| 2026-07 | EU | CAMX XSTO | Camurus | Phase 3 | A Trial to Assess Efficacy and Safety of Octreotide Subcutaneous Depot in Patients With GEP-NET |
| 2026-07-31 | EU | ORNBV XHEL | Orion Corporation | Phase 1/Phase 2 | Safety and Pharmacokinetics of ODM-208 in Patients With Metastatic Castration-resistant Prostate Cancer |
| 2026-08 | EU | ARGX XBRU | argenx | Phase 2 | A Safety and Efficacy Study of ARGX-119 in Adult Patients With Amyotrophic Lateral Sclerosis (ALS) |
| 2026-08-13 | EU | ZEAL XCSE | Zealand Pharma | Phase 2 | Efficacy and Safety of Petrelintide in Participants With Overweight or Obesity and Type 2 Diabetes (ZUPREME 2) |
| 2026-08-17 | EU | BIOA-B XSTO | BioArctic | Phase 2 | Safety, Tolerability, and Pharmacokinetics of Exidavnemab in Patients With Parkinson's Disease and Patients With Multiple System Atrophy |
| 2026-09 | EU | ARGX XBRU | argenx | Phase 3 | A Study to Assess the Efficacy and Safety of Empasiprubart Versus IVIg in Adults With Multifocal Motor Neuropathy |
| 2026-09-30 | EU | ARGX XBRU | argenx | Phase 2/Phase 3 | A Study of Efgartigimod PH20 SC in Children Between 2 and Less Than 18 Years of Age With Generalized Myasthenia Gravis |
| 2026-10 | EU | PHARM XAMS | Pharming | Phase 2 | Leniolisib for Immune Dysregulation in CVID |
| 2026-10 | EU | PHIL XMIL | Philogen | Phase 1/Phase 2 | Safety and Efficacy of L19TNF Plus Temozolomide Chemoradiotherapy in Patients With Newly Diagnosed Glioblastoma |
| 2026-10-01 | EU | ARGX XBRU | argenx | Phase 3 | A Phase 3 Study to Evaluate the Safety and Efficacy of Efgartigimod PH20 Subcutaneous in Adult Patients With Primary Immune Thrombocytopenia |
| 2026-10-05 | EU | SOBI XSTO | Swedish Orphan Biovitrum | Phase 3 | A Phase 3 Study of Pacritinib in Patients With Primary Myelofibrosis, Post Polycythemia Vera Myelofibrosis, or Post-Essential Thrombocythemia Myelofibrosis |
| 2026-11 | EU | DBV XPAR | DBV Technologies | Phase 3 | Safety Study of Viaskin® Peanut Patch in Peanut-Allergic Children 1 Through 3 Years of Age (COMFORT Toddlers) |
| 2026-11 | EU | ARGX XBRU | argenx | Phase 2 | A Study to Evaluate Safety and Efficacy of Empasiprubart in Adults With Dermatomyositis |
| 2026-11 | EU | PHARM XAMS | Pharming | Phase 2 | Leniolisib for Immune Dysregulation in PIDs |
| 2026-11-30 | EU | PHARM XAMS | Pharming | Phase 3 | Pediatric Patients Aged 4 to 11 Years With APDS |
| 2026-11-30 | EU | BAVA XCSE | Bavarian Nordic | Phase 2 | Comparability Trial of the MVA-BN Vaccine Manufactured in Different Production Cells |
| 2026-12 | EU | ABVX XPAR | Abivax | Phase 2 | Efficacy and Safety of Obefazimod in Subjects With Moderately to Severely Active Crohn's Disease |
| 2026-12-01 | EU | ARGX XBRU | argenx | Phase 2/Phase 3 | A Study to Investigate the Efficacy and Safety of Efgartigimod PH20 SC in Adult Participants With Active Idiopathic Inflammatory Myopathy. |
| 2026-12-04 | EU | VLA XPAR | Valneva | Phase 3 partner: Pfizer | A Study to Learn About the Safety, Tolerability, and Immunogenicity of a Fifth Dose of 6-Valent OspA-Based Lyme Disease Vaccine |
| 2026-12-30 | EU | SOBI XSTO | Swedish Orphan Biovitrum | Phase 2 | A Study to Assess the Effectiveness and Safety of Pacritinib in Patients With VEXAS Syndrome (PAXIS) |
| 2026-12-31 | EU | NWRN XSWX | Newron Pharmaceuticals | Phase 3 | Evenamide, a Glutamate Release Modulator, as Add-On to Standard of Care in Subjects With Documented Treatment-Resistant Schizophrenia |
| 2027-02 | EU | ARGX XBRU | argenx | Phase 2 | A Study to Assess the Efficacy and Safety of Efgartigimod PH20 SC in Adults With Systemic Sclerosis |
| 2027-02 | EU | GMAB XCSE | Genmab | Phase 3 | Study to Assess the Efficacy of Rina-S Compared to Treatment of Investigator's Choice in Participants With Platinum Resistant Ovarian Cancer |
| 2027-02 | EU | BAVA XCSE | Bavarian Nordic | Phase 2 | A Phase 2 Trial in Healthy Adult Participants of the Recombinant MVA-BN-WEV Vaccine |
| 2027-02 | EU | ALM* XMAD | Almirall | Phase 2 | A Proof-of-Concept Study of LAD328 in Adults With Hidradenitis Suppurativa |
| 2027-02-28 | EU | HNSA XSTO | Hansa Biopharma | Phase 2 | Imlifidase Prior to Kidney Transplant in Highly Sensitised Children |
| 2027-03 | EU | ARGX XBRU | argenx | Phase 2/Phase 3 | Evaluating the Pharmacokinetics, Pharmacodynamics, and Safety of Efgartigimod Administered Intravenously in Children With Generalized Myasthenia Gravis |
| 2027-03 | EU | GMAB XCSE | Genmab | Phase 2 | A Study to Evaluate Adverse Events of Subcutaneous (SC) Epcoritamab Administered in the Outpatient Setting in Adult Participants With Relapsed or Refractory Diffuse Large B-Cell Lymphoma and Classic Follicular Lymphoma |
| 2027-03 | EU | SOBI XSTO | Swedish Orphan Biovitrum | Phase 3 | Study to Provide Continued Access to Treatment for Patients Completing a Previous Trial With Efanesoctocog Alfa |
| 2027-03 | EU | FARON* XHEL | Faron Pharmaceuticals | Phase 1/Phase 2 | A Study to Assess Safety, Tolerability and Preliminary Efficacy of Bexmarilimab in Combination With Standard of Care in Patients With Hematological Malignancies |
| 2027-04-25 | EU | ALM* XMAD | Almirall | Phase 3 | A Study of Lebrikizumab Treatment in Adults and Adolescents With Moderate-to-Severe Atopic Dermatitis |
| 2027-04-30 | EU | ARGX XBRU | argenx | Phase 2 | A Study to Assess the Long-term Safety and Efficacy of a Subcutaneous Formulation of Efgartigimod in Adults With Chronic Inflammatory Demyelinating Polyneuropathy (CIDP, an Autoimmune Disorder That Affects the Peripheral Nerves) |
| 2027-05 | EU | VICO XSTO | Vicore Pharma | Phase 2 | A Trial to Evaluate Efficacy and Safety of Buloxibutid in People With Idiopathic Pulmonary Fibrosis. |
| 2027-05-25 | EU | ALM* XMAD | Almirall | Phase 2 | A Study of LAD191 in Adults With Hidradenitis Suppurativa |
| 2027-06 | EU | IPH XPAR | Innate Pharma | Phase 2 | IPH5201 and Durvalumab in Patients With Resectable Non-Small Cell Lung Cancer (MATISSE) |
| 2027-06 | EU | ALBPS XPAR | Biophytis | Phase 2 | Testing the Efficacy, Safety, and PK of 20E in Patients With Obesity Who Are Starting Treatment With the GLP-1 Agonist Semaglutide for Weight Loss. |
| 2027-06 | EU | GMAB XCSE | Genmab | Phase 3 | A Study to Evaluate Change in Disease Activity of Subcutaneous (SC) Epcoritamab Combined With Intravenous and Oral Rituximab, Cyclophosphamide, Doxorubicin Hydrochloride, Vincristine, and Prednisone (R-CHOP) or R-CHOP in Adult Participants With Newly Diagnosed Diffuse Large B-Cell Lymphoma (DLBCL) |
| 2027-06 | EU | IDIA XSWX | Idorsia | Phase 2 | A Study to Learn How Safe ACT-777991 is and How Well it Works in Adults With Non-segmental Vitiligo |
| 2027-06-23 | EU | ALM* XMAD | Almirall | Phase 2 | A Study of LAD603 in Adults With Alopecia Areata |
| 2027-07 | EU | ALSEN XPAR | Sensorion | Phase 1/Phase 2 | A Phase I/II Clinical Trial With SENS-501 in Children Suffering From Severe to Profound Hearing Loss Due to Otoferlin (OTOF) Mutations |
| 2027-07 | EU | ARGX XBRU | argenx | Phase 3 | A Study of the Efficacy and Safety of Efgartigimod in Patients With Primary Sjögren's Syndrome |
| 2027-07 | EU | GMAB XCSE | Genmab | Phase 1/Phase 2 | Rinatabart Sesutecan (Rina-S, PRO1184, GEN1184) for Advanced Solid Tumors (GCT1184-01/ PRO1184-001) |
| 2027-07-30 | EU | GMAB XCSE | Genmab | Phase 3 | Trial to Evaluate Acasunlimab and Pembrolizumab Combination Superiority Over Standard of Care Docetaxel in Non-Small Cell Lung Cancer (ABBIL1TY NSCLC-06) |
| 2027-08 | EU | GNFT XPAR | Genfit | Phase 2 | Phase 2 Study of 500 mg BID NTZ on Top of Standard of Care in Patients With Acute Decompensation of Liver Cirrhosis at High Risk of Progression to Acute-on-Chronic Liver Failure or Established Acute-on-Chronic Liver Failure |
| 2027-09 | EU | ARGX XBRU | argenx | Phase 3 | A Study to Assess Efficacy and Safety of Empasiprubart Versus IVIg in Adults With CIDP |
| 2027-09 | EU | GMAB XCSE | Genmab | Phase 3 | An Extension Study to Assess the Efficacy of Rina-S Compared to Treatment of Investigator's Choice in Participants With Platinum Resistant Ovarian Cancer in China |
| 2027-09 | EU | GMAB XCSE | Genmab | Phase 1/Phase 2 | Trial of the Safety and Efficacy of Epcoritamab in Japanese Subjects With Relapsed or Refractory (R/R) B-Cell Non-Hodgkin Lymphoma (R/R B-NHL) |
| 2027-09 | EU | NYKD XOSL | Nykode Therapeutics | Phase 1/Phase 2 | Safety and Efficacy of VB10.16 and Pembrolizumab in Patients with Head-Neck Squamous Cell Carcinoma |
| 2027-09-30 | EU | IVA XPAR | Inventiva | Phase 3 | A Phase 3 Study Evaluating Efficacy and Safety of Lanifibranor Followed by an Active Treatment Extension in Adult Patients With (NASH) and Fibrosis Stages F2 and F3 ( NATiV3 ) |
| 2027-09-30 | EU | GMAB XCSE | Genmab | Phase 1/Phase 2 | Safety and Efficacy Trial of Epcoritamab Combinations in Subjects With B-cell Non-Hodgkin Lymphoma (B-NHL) |
| 2027-10 | EU | ARGX XBRU | argenx | Phase 2 | ADAPT Forward 2 – ISA2 – a Study to Evaluate the Safety, Tolerability and Efficacy of Empasiprubart IV Monotherapy in Participants With AChR-Ab Seropositive Generalized Myasthenia Gravis |
| 2027-10 | EU | PHARM XAMS | Pharming | Phase 2 | Efficacy of KL1333 in Adult Patients With Primary Mitochondrial Disease |
| 2027-10-07 | EU | ARGX XBRU | argenx | Phase 3 | A Study to Assess the Efficacy and Safety of Empasiprubart in Adults With CIDP |
| 2027-11 | EU | ARGX XBRU | argenx | Phase 2 | A Study to Evaluate the Safety and Tolerability of Efgartigimod PH20 SC Given by Prefilled Syringe in Kidney Transplant Recipients With Antibody-Mediated Rejection (AMR) |
| 2027-11-12 | EU | ZEAL XCSE | Zealand Pharma | Phase 2 partner: Roche | A Dose-Finding Study of Petrelintide With Enicepatide (RO7795068) in Adults With Obesity or Overweight |
| 2027-11-22 | EU | GMAB XCSE | Genmab | Phase 2 | Study to Assess the Efficacy and Safety of Rina-S in Participants With Non-small Cell Lung Cancer |
| 2027-11-30 | EU | FARON* XHEL | Faron Pharmaceuticals | Phase 2 | Bexmarilimab + Azacitidine Versus Placebo + Azacitidine in Participants With Treatment-naïve Higher-risk Myelodysplastic Syndromes |
| 2027-12 | EU | GNFT XPAR | Genfit | Phase 1/Phase 2 | Combination of GNS561 and Trametinib in Patients With Advanced KRAS Mutated Cholangiocarcinoma |
| 2027-12 | EU | GMAB XCSE | Genmab | Phase 1/Phase 2 | Safety and Efficacy Study of Epcoritamab in Subjects With Relapsed/Refractory Chronic Lymphocytic Leukemia and Richter's Syndrome |
| 2027-12 | EU | PHIL XMIL | Philogen | Phase 3 | Efficacy of Daromun Neoadjuvant Intratumoral Treatment in Clinical Stage IIIB/C/D Melanoma Patients |
| 2027-12-15 | EU | OSE XPAR | OSE Immunotherapeutics | Phase 3 | Trial of Therapeutic Cancer Vaccine OSE2101 in Patients With Non-Small Cell Lung Cancer and Secondary Resistance to Immune Checkpoint Inhibitor |
| 2027-12-30 | EU | TNG XPAR | Transgene | Phase 1/Phase 2 | A Clinical Trial Evaluating TG4050 in Head and Neck Cancer |
| 2027-12-31 | EU | ORNBV XHEL | Orion Corporation | Phase 1/Phase 2 | A Phase 1/2, First-in-Human Study On ODM-212 In Subjects With Selected Advanced Solid Tumours |
| 2028-01-27 | EU | VLA XPAR | Valneva | Phase 3 partner: Pfizer | A Study to Learn About Different Dosing Schedules of a Lyme Disease Vaccine in Healthy Adults |
| 2028-01-30 | EU | BSLN XSWX | Basilea Pharmaceutica | Phase 3 | A Phase 3 Efficacy and Safety Study of Fosmanogepix for the Treatment of Adult Participants With Candidemia and/or Invasive Candidiasis. |
| 2028-02 | EU | BSLN XSWX | Basilea Pharmaceutica | Phase 3 | A Phase 3 Efficacy and Safety Study of Fosmanogepix for the Treatment of Adult Patients With Invasive Mold Infections. |
| 2028-03 | EU | ABVX XPAR | Abivax | Phase 2 | Long-term Safety and Efficacy Profile of ABX464 in Subjects With Moderate to Severe Active Ulcerative Colitis |
| 2028-03 | EU | GMAB XCSE | Genmab | Phase 3 | A Study of Subcutaneously Injected Epcoritamab Plus Oral Lenalidomide Tablets Compared to Intravenously (IV) Infused Rituximab Plus IV Infused Gemcitabine and IV Infused Oxaliplatin in Adult Participants With Relapsed or Refractory Diffuse Large B-Cell Lymphoma |
| 2028-03 | EU | HPHA XFRA | Heidelberg Pharma | Phase 1/Phase 2 | Study to Assess Safety of HDP-101 in Patients With Relapsed Refractory Multiple Myeloma |
| 2028-03-07 | EU | ARGX XBRU | argenx | Phase 2 | ADAPT Forward 1 – ISA1 – a Study to Evaluate Empasiprubart IV as add-on Therapy to Efgartigimod IV in Participants With AChR-Ab Seropositive Generalized Myasthenia Gravis With a Partial Clinical Response to Efgartigimod |
| 2028-04 | EU | ARGX XBRU | argenx | Phase 2/Phase 3 | A Study to Assess the Correct Dose, Safety and Efficacy of Empasiprubart in Adolescent Participants Aged 12 to Less Than 18 Years With Chronic Inflammatory Demyelinating Polyradiculoneuropathy |
| 2028-04 | EU | BAVA XCSE | Bavarian Nordic | Phase 3 | Long-term Follow-up Study to Evaluate Safety and Immunogenicity of PXVX0317 Single or Booster Vaccination |
| 2028-05-10 | EU | ORNBV XHEL | Orion Corporation | Phase 3 partner: MSD | A Study of Opevesostat (MK-5684) Versus Alternative Next-generation Hormonal Agent (NHA) in Metastatic Castration-resistant Prostate Cancer (mCRPC) Post One NHA (MK-5684-004) |
| 2028-06 | EU | ARGX XBRU | argenx | Phase 3 | A Study to Assess the Efficacy and Safety of Efgartigimod IV in Adult Participants With Primary Immune Thrombocytopenia |
| 2028-06 | EU | ARGX XBRU | argenx | Phase 3 | A Study to Assess Efficacy and Safety of Efgartigimod PH20 SC PFS in Adult Participants With Graves' Disease. |
| 2028-06 | EU | ARGX XBRU | argenx | Phase 3 | A Study to Assess Efficacy and Safety of Efgartigimod PH20 SC PFS in Adult Participants With Graves' Disease |
| 2028-06-30 | EU | NANO XPAR | Nanobiotix | Phase 3 partner: Johnson & Johnson | JNJ-90301900 (NBTXR3) Activated by Radiotherapy With or Without Cetuximab in LA-HNSCC |
| 2028-07 | EU | PHIL XMIL | Philogen | Phase 2 | Study of the Efficacy of Intratumoral L19IL2 or L19TNF or L19IL2/L19TNF, in Combination with Pembrolizumab, in Unresectable Melanoma Patients |
| 2028-07-09 | EU | PHARM XAMS | Pharming | Phase 3 | Pediatric Patients Aged 1 to 6 Years With APDS |
| 2028-08 | EU | ALM* XMAD | Almirall | Phase 3 | A Study of Lebrikizumab in Adults With Nummular Eczema |
| 2028-08-02 | EU | ORNBV XHEL | Orion Corporation | Phase 3 partner: MSD | Study of Opevesostat (MK-5684) Versus Alternative NHA in mCRPC (MK-5684-003) |
| 2028-09 | EU | ARGX XBRU | argenx | Phase 3 | A Study to Assess the Long-term Safety and Efficacy of a Subcutaneous Formulation of Efgartigimod in Adults With Active Idiopathic Inflammatory Myopathy |
| 2028-09 | EU | GMAB XCSE | Genmab | Phase 2 | Study to Assess the Efficacy and Safety of Rina-S in Participants With Advanced Gastrointestinal (GI) Cancers |
| 2028-09 | EU | MOLN XSWX | Molecular Partners | Phase 1/Phase 2 | Study of [212Pb]Pb-DOTAM-MAM279 ([212Pb]Pb-MP0712) in Patients With Small Cell Lung Cancer and Other DLL3 Expressing Solid Tumors |
| 2028-09-18 | EU | PHARM XAMS | Pharming | Phase 2 | Long-term Safety and Efficacy of Leniolisib in PIDs With Immune Dysregulation |
| 2028-09-18 | EU | ZEAL XCSE | Zealand Pharma | Phase 3 | Efficacy and Safety Evaluation of Glepaglutide in Treatment of Short Bowel Syndrome |
| 2028-10 | EU | ARGX XBRU | argenx | Phase 2/Phase 3 | A Study of Efgartigimod IV in Participants From 12 Years to Less Than 18 Years of Age With Chronic Immune Thrombocytopenia (ITP) |
| 2028-10 | EU | GMAB XCSE | Genmab | Phase 3 | Study to Assess the Efficacy and Safety of Rina-S Plus Standard of Care Compared to Standard of Care for Maintenance Treatment of Participants With Recurrent Platinum-sensitive Ovarian Cancer After Second-line (2L) Platinum-based Doublet Chemotherapy |
| 2028-10-23 | EU | ZEAL XCSE | Zealand Pharma | Phase 3 | Efficacy And Safety Evaluation of Glepaglutide in Treatment of SBS |
| 2028-12 | EU | BAVA XCSE | Bavarian Nordic | Phase 3 | A Safety and Immunogenicity Study of CHIKV VLP Vaccine in Children. |
| 2029-01 | EU | GMAB XCSE | Genmab | Phase 1/Phase 2 | First-in-Human (FIH) Trial in Patients With Relapsed, Progressive or Refractory B-Cell Lymphoma |
| 2029-01-15 | EU | ORNBV XHEL | Orion Corporation | Phase 1/Phase 2 partner: MSD | Substudy 01A: Safety and Efficacy of Opevesostat (MK-5684)-Based Treatment Combinations or Opevesostat Alone in Participants With Metastatic Castration-resistant Prostate Cancer (mCRPC) (MK-5684-01A) |
| 2029-01-30 | EU | PHIL XMIL | Philogen | Phase 2 | A Study to Evaluate the Safety and Efficacy of L19TNF With Alkylating Chemotherapy for Patients With Recurrent IDH-mutant Astrocytoma or Oligodendroglioma |
| 2029-03-31 | EU | PHARM XAMS | Pharming | Phase 2 | Open Label Extension to Assess Long Term Safety and Efficacy of KL1333 in Patients With Primary Mitochondrial Disease |
| 2029-04-02 | EU | PHM* XMAD | PharmaMar | Phase 1/Phase 2 | Study of PM54 in Combination With Immunotherapy in Adult Participants With Advanced Malignancies |
| 2029-05-28 | EU | ARGX XBRU | argenx | Phase 2 | A Study to Assess the Safety, Tolerability, Efficacy, Pharmacokinetics, and Immunogenicity of Intravenous Administration of ARGX-119 in Pediatric Participants Aged 5 to Less Than 18 Years With Spinal Muscular Atrophy |
| 2029-06 | EU | PRTC XLON | PureTech | Phase 3 | Trial to Evaluate the Efficacy and Safety of LYT-100 (Deupirfenidone) Compared to Pirfenidone in Adults With Idiopathic Pulmonary Fibrosis (IPF) |
| 2029-07 | EU | GMAB XCSE | Genmab | Phase 3 | Study of Petosemtamab Plus Chemotherapy Versus Cetuximab Plus Chemotherapy in RAS and BRAF Wild-type, Unresectable or Metastatic, Left-sided Colorectal Cancer |
| 2029-08 | EU | GMAB XCSE | Genmab | Phase 3 | Study to Assess the Efficacy and Safety of Rina-S Compared to Treatment of Investigator's Choice in Participants With Endometrial Cancer |
| 2029-08 | EU | IDIA XSWX | Idorsia | Phase 3 | A Study to Evaluate the Long-term Safety and Tolerability of Lucerastat in Adult Subjects With Fabry Disease |
| 2029-08-30 | EU | PHM* XMAD | PharmaMar | Phase 3 | Study of Lurbinectedin in Combination With Doxorubicin Versus Doxorubicin Alone as First-line Treatment in Participants With Metastatic Leiomyosarcoma (SaLuDo) |
| 2029-09 | EU | ARGX XBRU | argenx | Phase 2/Phase 3 | Evaluating Long-term Safety of Efgartigimod Administered Intravenously and Efgartigimod PH20 Administered Subcutaneously in Children With Generalized Myasthenia Gravis |
| 2029-09 | EU | ORNBV XHEL | Orion Corporation | Phase 1/Phase 2 | A 2-part Phase 1/2 Open-label Trial on ODM-212 |
| 2029-09-30 | EU | ARGX XBRU | argenx | Phase 2 | A Clinical Trial to Investigate the Long-term Safety and Tolerability, Efficacy, Pharmacodynamics, Pharmacokinetics, and Immunogenicity of ARGX-117 in Adults With Multifocal Motor Neuropathy |
| 2029-12 | EU | OSE XPAR | OSE Immunotherapeutics | Phase 1/Phase 2 | Dose-finding and Dose Expansion Study of OSE-279 in Subjects With Advanced Solid Tumors or Lymphomas |
| 2029-12 | EU | GMAB XCSE | Genmab | Phase 3 | Study to Assess the Efficacy and Safety of Rina-S With or Without Bevacizumab Compared to Investigator's Choice of Platinum-based Chemotherapy With or Without Bevacizumab as Second-line Treatment in Participants With Recurrent Platinum-sensitive Ovarian Cancer |
| 2029-12 | EU | GMAB XCSE | Genmab | Phase 3 | Study of Subcutaneous Epcoritamab in Combination With Intravenous Rituximab and Oral Lenalidomide (R2) to Assess Adverse Events and Change in Disease Activity in Adult Participants With Follicular Lymphoma |
| 2030-04-30 | EU | HNSA XSTO | Hansa Biopharma | Phase 3 | A Long-term Follow-up Trial of Patients Previously Treated With Imlifidase Prior to Kidney Transplantation and a Non-comparative Transplanted Patient Group |
| 2030-05 | EU | BAVA XCSE | Bavarian Nordic | Phase 3 | An Efficacy, Safety, and Immunogenicity Study of CHIKV VLP Vaccine for the Prevention of Chikungunya Disease in Adolescents and Adults |
| 2030-12 | EU | GMAB XCSE | Genmab | Phase 1/Phase 2 partner: BioNTech | A Clinical Study to Test if an Investigational Treatment Called BNT314 When Used in Combination With Another Investigational Treatment Pumitamig (BNT327) and Chemotherapy, is Beneficial and Safe for Patients With Advanced Colorectal Cancer |
| 2030-12-04 | EU | ARGX XBRU | argenx | Phase 2 | A Study to Learn About How Well the Medicine Efgartigimod Works to Treat Autoimmune Encephalitis In Children 12 Years or Older and Adults |
| 2031-02 | EU | PHIL XMIL | Philogen | Phase 2 | L19IL2/TNF in Patients With Basal Cell Carcinoma |
| 2031-02 | EU | PHIL XMIL | Philogen | Phase 2 | L19IL2/L19TNF in Patients With Cutaneous Squamous Cell Carcinoma |
| 2031-02 | EU | PHIL XMIL | Philogen | Phase 2 | L19IL2 or L19TNF or L19IL2/TNF in Patients With Basal Cell Carcinoma (BCC) |
| 2032-11 | EU | GMAB XCSE | Genmab | Phase 2 | A Study to Evaluate Adverse Events and Change in Disease Activity of Subcutaneous (SC) Epcoritamab in Combination With Oral and Intravenous Anti-Neoplastic Agents in Adult Participants With Non-Hodgkin Lymphoma |
| 2037-11 | EU | GMAB XCSE | Genmab | Phase 3 | Study of Subcutaneous Epcoritamab in Combination With Intravenous Rituximab and Oral Lenalidomide (R2) to Assess Adverse Events and Change in Disease Activity in Adult Participants With Previously Untreated Follicular Lymphoma |
| 2026-07-21 | Ex-US | CHIZF | China Traditional Chinese Medicine Holdings Co. Limited | Phase 2 | CD22/CD19 CAR-T and Auto-HSCT Sandwich Strategy as Consolidation Therapy for B-ALL |
| 2026-07-26 | US | MNKD | MannKind | PDUFA | |
| 2026-07-30 | US | CERS | Cerus Corporation | Phase 2 | A Recovery and Lifespan Study Using INTERCEPT Red Blood Cells Prepared Using the INTERCEPT Blood System for RBCs With AS-1 |
| 2026-07-30 | US | QNRX | Quoin Pharmaceuticals, Ltd. | Phase 3 | Clinical Study of QRX003 Lotion in Subjects With Netherton Syndrome |
| 2026-07-31 | US | CERS | Cerus Corporation | Phase 3 | INTERCEPT Blood System for RBCs Study in Regions at Potential Risk for Zika Virus Transfusion-Transmitted Infections |
| 2026-07-31 | US | OCGN | Ocugen, Inc. | Phase 1 | Phase I Study to Assess the Safety and Efficacy of OCU200 for Center-Involved Diabetic Macular Edema (DME) |
| 2026-08-01 | Ex-US | ABSCF | AB Science S.A. | Phase 2 | AB8939 in Patients With Relapsed/Refractory Acute Myeloid Leukemia |
| 2026-08-01 | US | ACIU | AC Immune SA | Phase 1 | A Study Investigating the Safety, Absorption, Elimination, and the Effect on the Immune System of ACI-19764 in Healthy Participants |
| 2026-08-01 | US | ACRS | Aclaris Therapeutics, Inc. | Phase 2 | ATI-045 Versus Placebo in Patients With Moderate-to-Severe Atopic Dermatitis |
| 2026-08-01 | US | AKBA | Akebia Therapeutics, Inc. | Phase 3 | To Evaluate the Efficacy of Three Times Weekly (TIW) Vadadustat Compared to Standard of Care ESA in Patients With Anemia of CKD Receiving In-Center Hemodialysis |
| 2026-08-01 | US | ANRO | Alto Neuroscience, Inc. | Phase 2 | ALTO-100 in Bipolar Disorder With Depression (BD-D) |
| 2026-08-01 | Ex-US | ASCLF | Ascletis Pharma Inc. | Phase 2 | A Study to Evaluate the Efficacy, Safety, and Tolerability of ASC30 Tablets in Participants With Type 2 Diabetes Mellitus |
| 2026-08-01 | US | BHVN | Biohaven Ltd. | Phase 1 | A Surgical Window of Opportunity Clinical Trial of Troriluzole in Recurrent IDH Wild-Type Glioblastoma |
| 2026-08-01 | US | CADL | Candel Therapeutics, Inc. | Phase 2 | A Biomarker Study in Men With Localized Prostate Cancer Treated With Aglatimagene Besadenovec |
| 2026-08-01 | Ex-US | CASBF | CanSino Biologics Inc. | Phase 1 | A Study to Evaluate the Safety and Immunogenicity of Ad5-105K in Adults Aged 18 to 49 Years |
| 2026-08-01 | US | CORT | Corcept Therapeutics Incorporated | Phase 2 | Relacorilant in Combination With Different Treatment Regimens in Patients With Gynecological Cancers |
| 2026-08-01 | US | CORT | Corcept Therapeutics Incorporated | Phase 2 | Relacorilant in Combination With Different Treatment Regimens in Patients With Gynecological Cancers |
| 2026-08-01 | US | CPHI | China Pharma Holdings, Inc. | Phase 2 | A Study to Evaluate the Efficacy, Safety, and Tolerability of ASC30 Tablets in Participants With Type 2 Diabetes Mellitus |
| 2026-08-01 | US | CRIS | Curis, Inc. | Phase 2 | CA-4948-101: Open-Label, Dose Escalation and Expansion Trial of Emavusertib (CA-4948) in Relapsed or Refractory Primary Central Nervous System Lymphoma (R/R PCNSL) |
| 2026-08-01 | US | ENSC | Ensysce Biosciences, Inc. | Phase 3 | PF614 Analgesic Activity in Acute Postoperative Pain (PF614-301) |
| 2026-08-01 | US | EYPT | EyePoint, Inc. | Phase 3 | A 2-year Study of EYP-1901 in Subjects With Wet Age Related Macular Degeneration (wAMD) (LUGANO) Primary Efficacy Will be Determined at Week 56 |
| 2026-08-01 | US | GPCR | Structure Therapeutics Inc. | Phase 2 | Aleniglipron Phase 2 Body Composition Study |
| 2026-08-01 | US | HELP | Cybin Inc. | Phase 3 | A Study of a Deuterated Psilocin Analog (CYB003) in Humans With Major Depressive Disorder |
| 2026-08-01 | US | IGC | IGC Pharma, Inc. | Phase 2 | Clinical Trial on Agitation in Alzheimer's Dementia |
| 2026-08-01 | US | IVVD | Invivyd, Inc. | Phase 3 | Study of VYD2311 for the Prevention of COVID-19 |
| 2026-08-01 | US | IVVD | Invivyd, Inc. | Phase 3 | Safety and Serum Virus Neutralizing Antibody Responses of VYD2311, a COVID-19 Vaccine, and Coadministered VYD2311 With a COVID-19 Vaccine |
| 2026-08-01 | Ex-US | JBPHF | Jacobio Pharmaceuticals Group Co., Ltd. | Phase 2 | JAB-2485 Activity in Adult Patients With Advanced Solid Tumors |
| 2026-08-01 | US | KOD | Kodiak Sciences Inc. | Phase 3 | A Study to Evaluate the Efficacy and Safety of Tarcocimab Tedromer and Tabirafusp Tedromer Compared to Aflibercept in Participants With Neovascular (Wet) Age-related Macular Degeneration (wAMD) – DAYBREAK |
| 2026-08-01 | US | KPTI | Karyopharm Therapeutics Inc. | Phase 3 | Selinexor in Maintenance Therapy After Systemic Therapy for Participants With p53 Wild-Type, Advanced or Recurrent Endometrial Carcinoma |
| 2026-08-01 | US | KURA | Kura Oncology, Inc. | Phase 1 | Safety and Tolerability of Ziftomenib Combinations in Patients With Relapsed/Refractory Acute Myeloid Leukemia |
| 2026-08-01 | US | KYTX | Kyverna Therapeutics, Inc. | Phase 2 | KYSA-1: A Study of Anti-CD19 Chimeric Antigen Receptor T-Cell (CD19 CAR T) Therapy, in Subjects With Refractory Lupus Nephritis |
| 2026-08-01 | US | MIRM | Mirum Pharmaceuticals, Inc. | Phase 3 | A Trial Evaluating Brelovitug vs Delayed Treatment for the Treatment of Chronic Hepatitis Delta Infection (AZURE-4) |
| 2026-08-01 | US | MPLT | MapLight Therapeutics, Inc. | Phase 2 | A Study to Assess the Efficacy and Safety of ML-007C-MA for the Treatment of Inpatient Adults With Schizophrenia |
| 2026-08-01 | Ex-US | MRCHF | H.U. Group Holdings, Inc. | Phase 3 | Comparison of Azathioprine to Methotrexate in Combination Therapy With Adalimumab in Crohn's Disease: an Open-label Randomized Controlled Trial |
| 2026-08-01 | US | NCNA | NuCana plc | Phase 2 | A Safety, Pharmacokinetic and Clinical Activity Study of NUC-7738 in Patients With Advanced Solid Tumours and Lymphoma |
| 2026-08-01 | US | PHVS | Pharvaris N.V. | Phase 3 | Study of Oral Deucrictibant Extended-Release Tablet for Prophylaxis Against Angioedema Attacks in Adolescents and Adults With HAE |
| 2026-08-01 | US | RCUS | Arcus Biosciences, Inc. | Phase 2 | Study of Novel Treatment Combination Therapies in Participants With Head and Neck Squamous Cell Carcinoma Regardless of PD-L1 Expression Status; Substudy-01 |
| 2026-08-01 | US | RGNX | REGENXBIO Inc. | Phase 2 | RGX-314 Gene Therapy Administered in the Suprachoroidal Space for Participants With Neovascular Age-Related Macular Degeneration (nAMD) |
| 2026-08-01 | US | RGNX | REGENXBIO Inc. | Phase 3 | AFFINITY DUCHENNE: RGX-202 Gene Therapy in Participants With Duchenne Muscular Dystrophy (DMD) |
| 2026-08-01 | US | RGNX | REGENXBIO Inc. | Phase 2 | RGX-314 Gene Therapy Administered in the Suprachoroidal Space for Participants With Neovascular Age-Related Macular Degeneration (nAMD) |
| 2026-08-01 | US | RIGL | Rigel Pharmaceuticals, Inc. | Phase 2 | Study of R289 in Patients With Lower-risk Myelodysplastic Syndromes (LR MDS) |
| 2026-08-01 | US | RNA | Avidity Biosciences, Inc. | Phase 3 | Global Study of Del-desiran for the Treatment of DM1 |
| 2026-08-01 | US | SLGL | Sol-Gel Technologies Ltd. | Phase 3 | Efficacy and Safety of Patidegib Gel 2% for Preventing Basal Cell Carcinomas on the Face of Adults With Gorlin Syndrome |
| 2026-08-01 | US | VCNX | Vaccinex, Inc. | Phase 1 – Suspended | Adoptive T Cell Therapy Following HER2-Pulsed Dendritic Cell Vaccine & Pepinemab /Trastuzumab in Patients w/ Metastatic HER2+ Breast Cancer |
| 2026-08-01 | US | XENE | Xenon Pharmaceuticals Inc. | Phase 3 | A Randomized Study of Azetukalner Versus Placebo in Major Depressive Disorder |
| 2026-08-02 | US | REPL | Replimune, Inc. | PDUFA – CRL | |
| 2026-08-06 | US | MBIO | Mustang Bio, Inc. | Phase 1 | Genetically Modified T-cell Immunotherapy in Treating Patients With Relapsed/Refractory Acute Myeloid Leukemia and Persistent/Recurrent Blastic Plasmacytoid Dendritic Cell Neoplasm |
| 2026-08-12 | US | ACRV | Acrivon Therapeutics, Inc. | Phase 1 | Phase 1 Study of ACR-2316 in Specific Advanced Solid Tumors |
| 2026-08-13 | US | JSPR | Jasper Therapeutics, Inc. | Phase 2 | A Phase 2, Open-Label, Extension Study to Evaluate Long Term Safety and Clinical Activity of Briquilimab in Participants From Jasper-Sponsored Chronic Urticaria Trials |
| 2026-08-13 | US | LNTH | Lantheus Holdings, Inc. | PDUFA | |
| 2026-08-13 | Ex-US | ZLDPF | Zealand Pharma A/S | Phase 2 | Efficacy and Safety of Petrelintide in Participants With Overweight or Obesity and Type 2 Diabetes (ZUPREME 2) |
| 2026-08-15 | US | PMVP | PMV Pharmaceuticals, Inc. | Phase 2 | The Evaluation of PC14586 in Patients With Advanced Solid Tumors Harboring a TP53 Y220C Mutation (PYNNACLE) |
| 2026-08-19 | US | SYRE | Spyre Therapeutics, Inc. | Phase 1 | A Study of SPY002-091 in Healthy Volunteers |
| 2026-08-24 | US | SGMO | Sangamo Therapeutics, Inc. | Phase 1 | Safety Study of Zinc Finger Nuclease CCR5-modified Hematopoietic Stem/Progenitor Cells in HIV-1 Infected Patients |
| 2026-08-25 | US | CLRB | Cellectar Biosciences, Inc. | Phase 1 | Dose Escalation Study of CLR 131 in Pediatric Relapsed/Refractory Malignant Tumors Including Neuroblastoma and Sarcomas |
| 2026-08-30 | Ex-US | MSCLF | Satellos Bioscience Inc. | Phase 2 | An Open-label Long-term Follow-up Study of SAT-3247 for Participants With Duchenne Muscular Dystrophy Including Those Who Participated in SAT-3247-CL-101 |
| 2026-08-31 | US | IMMP | Immutep Limited | Phase 1 | A First-in-human Study of the Safety of an Immunosuppressive Antibody (IMP761) in Healthy Volunteers |
| 2026-08-31 | US | NRIX | Nurix Therapeutics, Inc. | Phase 1 | A Study of NX-1607 in Adults With Advanced Malignancies |
| 2026-08-31 | Ex-US | SNPHY | Santen Pharmaceutical Co., Ltd. | Phase 3 | A Phase III Study in Subjects With Primary Open Angle Glaucoma or Ocular Hypertension in China |
| 2026-08-31 | US | VSTM | Verastem, Inc. | Phase 2 | Study of Avutometinib (VS-6766) +Defactinib With Gemcitabine and Nab-paclitaxel in Patients With Pancreatic Cancer |
| 2026-09-01 | US | ARDX | Ardelyx, Inc. | Phase 3 | Study to Assess Safety and Efficacy of Tenapanor for Treatment of IBS-C in Pediatric Patients 12 to Less Than 18 Years |
| 2026-09-01 | US | ARQT | Arcutis Biotherapeutics, Inc. | Phase 2 | A Study for Evaluating Safety & Efficacy of Topical Roflumilast 0.3% Foam in Hidradenitis Suppurativa |
| 2026-09-01 | US | ARQT | Arcutis Biotherapeutics, Inc. | Phase 2 | A Study for Evaluating Safety & Efficacy of Topical Roflumilast 0.3% Foam in Hidradenitis Suppurativa |
| 2026-09-01 | US | ARVN | Arvinas, Inc. | Phase 2 | TACTIVE-U: A Study to Learn About the Study Medicine (Vepdegestrant) When Given With Other Medicines in People With Advanced or Metastatic Breast Cancer (Sub-Study A) |
| 2026-09-01 | US | ATXS | Astria Therapeutics, Inc. | Phase 1 | A Trial to Compare the Pharmacokinetics of Two Presentations of Navenibart in Healthy Participants |
| 2026-09-01 | US | AVIR | Atea Pharmaceuticals, Inc. | Phase 3 | C-BEYOND: Efficacy and Safety of BEM/RZR vs. SOF/VEL in Subjects With Chronic HCV |
| 2026-09-01 | US | BHVN | Biohaven Ltd. | Phase 2 | Taldefgrobep Alfa in Adults With Overweight and Obesity |
| 2026-09-01 | US | CGEM | Cullinan Therapeutics, Inc. | Phase 1 | A Study of CLN-619 (Anti-MICA/MICB Antibody) in Patients With Relapsed and Refractory Multiple Myeloma |
| 2026-09-01 | Ex-US | CLRPF | Clarity Pharmaceuticals Ltd | Phase 2 | 64Cu-SAR-bisPSMA and 67Cu-SAR-bisPSMA for Identification and Treatment of PSMA-expressing Metastatic Castrate Resistant Prostate Cancer (SECuRE) |
| 2026-09-01 | Ex-US | CLRPF | Clarity Pharmaceuticals Ltd | Phase 3 | Positron Emission Tomography Using 64Cu-SAR-bisPSMA in Participants With High-risk Prostate Cancer Prior to Radical Prostatectomy |
| 2026-09-01 | US | CORT | Corcept Therapeutics Incorporated | Phase 2 | A Phase 2b, Study Evaluating Miricorilant in Adult Patients With Nonalcoholic Steatohepatitis/Metabolic Dysfunction-Associated Steatohepatitis (MONARCH) |
| 2026-09-01 | US | CORT | Corcept Therapeutics Incorporated | Phase 2 | Two Part Study of Nenocorilant Combined With Nivolumab in Patients With Advanced Solid Malignancies |
| 2026-09-01 | US | CORT | Corcept Therapeutics Incorporated | Phase 2 | A Phase 2b, Study Evaluating Miricorilant in Adult Patients With Nonalcoholic Steatohepatitis/Metabolic Dysfunction-Associated Steatohepatitis (MONARCH) |
| 2026-09-01 | US | CRVO | CervoMed Inc. | Phase 2 | Clinical Study of Neflamapimod in Patients With Primary Progressive Aphasia |
| 2026-09-01 | US | DSGN | Design Therapeutics, Inc. | Phase 2 | DT-168 in Keratoplasty Patients With Fuchs Endothelial Corneal Dystrophy |
| 2026-09-01 | US | EWTX | Edgewise Therapeutics, Inc. | Phase 2 | Phase 2 Study of EDG-5506 in Becker Muscular Dystrophy (GRAND CANYON) |
| 2026-09-01 | US | IOVA | Iovance Biotherapeutics, Inc. | Phase 1 | KK-LC-1 TCR-T Cell Therapy for Gastric, Breast, Cervical, and Lung Cancer |
| 2026-09-01 | US | IRON | Disc Medicine, Inc. | Phase 2 | Study of DISC-0974 (RALLY-MF) in Participants With Myelofibrosis or Myelodysplastic Syndrome and Anemia |
| 2026-09-01 | US | IRON | Disc Medicine, Inc. | Phase 3 | Study of Bitopertin in Participants With EPP or XLP (APOLLO) |
| 2026-09-01 | US | KPTI | Karyopharm Therapeutics Inc. | Phase 2 | A Study to Evaluate Single Agent Selinexor Versus Physician's Choice in Participants With Previously Treated Myelofibrosis |
| 2026-09-01 | US | LEGN | Legend Biotech Corporation | Phase 1 | A Study of LUCAR-20SP in Subjects With Relapsed/Refractory B-cell Non-Hodgkin Lymphoma |
| 2026-09-01 | US | LXRX | Lexicon Pharmaceuticals, Inc. | Phase 1 | Comparison of Antiplatelet Effects of Sotagliflozin to FDA-approved Antiplatelet Drugs |
| 2026-09-01 | US | MAZE | Maze Therapeutics, Inc. | Phase 2 | A Phase 2 Study of MZE829 in Adults With APOL1 Kidney Disease |
| 2026-09-01 | US | NAMS | NewAmsterdam Pharma Company N.V. | Phase 2 | Evaluation of Obicetrapib on Antioxidant Levels in Plasma and HDL Particles of Healthy Volunteers |
| 2026-09-01 | US | NVCR | NovoCure Limited | Phase 2 | Optune Delivered Electric Field Therapy and Bevacizumab in Treating Patients With Recurrent or Progressive Grade 2 or 3 Meningioma |
| 2026-09-01 | US | ORIC | ORIC Pharmaceuticals, Inc. | Phase 2 | Study of ORIC-114 in Patients With Advanced Solid Tumors Harboring an EGFR or HER2 Alteration |
| 2026-09-01 | US | PCSA | Processa Pharmaceuticals, Inc. | Phase 2 | A Phase 2 Study of PCS6422 With Capecitabine in Patients With Advanced or Metastatic Breast Cancer |
| 2026-09-01 | US | RAPP | Rapport Therapeutics, Inc. | Phase 2 | Study Evaluating the Efficacy and Safety of RAP-219 in Adult Participants With Bipolar I Disorder |
| 2026-09-01 | US | SLN | Silence Therapeutics plc | Phase 2 | Study to Assess SLN124 in Patients With Polycythemia Vera |
| 2026-09-01 | US | SNDX | Syndax Pharmaceuticals, Inc. | Phase 2 | MAXPIRe: Study to Evaluate Axatilimab in Participants With Idiopathic Pulmonary Fibrosis (IPF) |
| 2026-09-01 | US | SUPN | Supernus Pharmaceuticals, Inc. | Phase 3 | Open-label Study to Evaluate Long-term Safety and Efficacy of SPN-812 (Viloxazine Extended-release Capsule) |
| 2026-09-01 | US | TYRA | Tyra Biosciences, Inc. | Phase 1 | Safety and Anti-Tumor Activity of TYRA-200 in Advanced Cholangiocarcinoma With Activating FGFR2 Gene Alterations |
| 2026-09-01 | US | VERA | Vera Therapeutics, Inc. | Phase 2 | Monthly Dosing of Atacicept in IgAN |
| 2026-09-01 | US | VERA | Vera Therapeutics, Inc. | Phase 2 | Monthly Dosing of Atacicept in IgAN |
| 2026-09-01 | US | VNDA | Vanda Pharmaceuticals Inc. | Phase 2 | Safety, Tolerability and Efficacy of Trichostatin A in Patients With Mild to Severe Onychomycosis |
| 2026-09-01 | US | VNDA | Vanda Pharmaceuticals Inc. | Phase 2 | An Eight-Week Study to Evaluate the Safety and Efficacy of VSJ-110 Compared to Placebo in the Treatment of Dry Eye |
| 2026-09-01 | US | VNDA | Vanda Pharmaceuticals Inc. | Phase 2 | Safety, Tolerability and Efficacy of Trichostatin A in Patients With Mild to Severe Onychomycosis |
| 2026-09-01 | US | VNDA | Vanda Pharmaceuticals Inc. | Phase 2 | An Eight-Week Study to Evaluate the Safety and Efficacy of VSJ-110 Compared to Placebo in the Treatment of Dry Eye |
| 2026-09-01 | US | VTVT | vTv Therapeutics Inc. | Phase 3 | Cadisegliatin as Adjunctive Therapy to Insulin in Participants With Type 1 Diabetes |
| 2026-09-01 | US | WVE | Wave Life Sciences Ltd. | Phase 2 | A Phase 1b/2a, Open-label Single Ascending Doses and Multiple Ascending Doses Study in Participants With Pi*ZZ AATD |
| 2026-09-04 | Ex-US | SHEZF | Shenzhen Hepalink Pharmaceutical Group Co., Ltd. | Phase 1 | A Clinical Study Evaluating H1710 for Injection in Participants With Advanced Solid Tumors |
| 2026-09-11 | Ex-US | NPPNY | Nippon Shinyaku Co., Ltd. | Phase 2 | NS-089/NCNP-02-201 in Boys With Duchenne Muscular Dystrophy (DMD) |
| 2026-09-15 | US | CORT | Corcept Therapeutics Incorporated | Phase 2 | REVERSE: Improving Treatment-resistant Post Traumatic Stress Disorder (PTSD) with Glucocorticoid Receptor (GR) Antagonism |
| 2026-09-15 | US | CORT | Corcept Therapeutics Incorporated | Phase 2 | REVERSE: Improving Treatment-resistant Post Traumatic Stress Disorder (PTSD) with Glucocorticoid Receptor (GR) Antagonism |
| 2026-09-21 | US | CRDL | Cardiol Therapeutics Inc. | Phase 3 | CardiolRx in Recurrent Pericarditis (MAVERIC Phase-3) |
| 2026-09-25 | US | VIR | Vir Biotechnology, Inc. | Phase 1 | Effect of Hepatic Impairment on the Pharmacokinetics and Safety of VIR-2218 and VIR-3434 |
| 2026-09-28 | US | MLTX | MoonLake Immunotherapeutics | Phase 3 | An Open-label, Single-arm Study to Evaluate Pharmacokinetics and Safety of Subcutaneous Sonelokimab in Adolescents With Moderate to Severe Hidradenitis Suppurativa (VELA-TEEN) |
| 2026-09-28 | US | OCGN | Ocugen, Inc. | Phase 3 | A Phase 2/3 Trial to Assess the Efficacy and Safety of OCU410ST for Stargardt Disease |
| 2026-09-30 | US | ALEC | Alector, Inc. | Phase 2 | Efficacy and Safety of GSK4527226 [AL101] in Participants With Early Alzheimer's Disease |
| 2026-09-30 | US | ATRA | Atara Biotherapeutics, Inc. | Phase 1 | Mesothelin-targeted CAR T-cell Therapy in Patients With Mesothelioma |
| 2026-09-30 | US | CERS | Cerus Corporation | Phase 2 – Withdrawn | Biotin-Acridine Red Cell Exchange Kinetics |
| 2026-09-30 | Ex-US | CHIZF | China Traditional Chinese Medicine Holdings Co. Limited | Phase 1 | The Safety and Efficacy of Pressurized Intraperitoneal Aerosol Chemotherapy for Peritoneal Metastatic Adenocarcinoma |
| 2026-09-30 | US | CHRS | Coherus Oncology, Inc. | Phase 1 | Study of CHS-114 in Participants With Advanced Solid Tumors |
| 2026-09-30 | US | MAJI | Marijuana Inc. | Phase 2 | Effects of CBD/CBD-A Oral Extract on Resting-state EEG and Neuropathic Pain Symptoms After SCI |
| 2026-09-30 | US | MJNA | Medical Marijuana, Inc. | Phase 2 | Effects of CBD/CBD-A Oral Extract on Resting-state EEG and Neuropathic Pain Symptoms After SCI |
| 2026-09-30 | US | QURE | uniQure N.V. | Phase 2 | Safety, Tolerability, and Exploratory Efficacy Study of Intrathecally Administered Gene Therapy AMT-162 in Adult Participants With SOD1 Amyotrophic Lateral Sclerosis (SOD1-ALS) |
| 2026-09-30 | US | RPTX | Repare Therapeutics Inc. | Phase 2 | A Study of RP-3500 in Combination With Standard Radiation Therapy in People With Solid Tumor Cancer |
| 2026-09-30 | Ex-US | SYMQY | SymBio Pharmaceuticals Limited | Phase 2 | A Phase 2a Study of IV BCV in Subjects With Adenovirus Infection |
| 2026-10-01 | US | ABOS | Acumen Pharmaceuticals, Inc. | Phase 2 | A Study to Evaluate Efficacy and Safety of Intravenous Sabirnetug in Participants With Early Alzheimer's Disease (ALTITUDE-AD) |
| 2026-10-01 | US | ADCT | ADC Therapeutics SA | Phase 2 | Loncastuximab Tesirine and Rituximab Followed by DA-EPOCH-R for Treating Patients With High-Risk Diffuse Large B-cell Lymphoma |
| 2026-10-01 | US | AGEN | Agenus Inc. | Phase 2 | Ivermectin in Combination With Balstilimab or Pembrolizumab in Patients With Metastatic Triple Negative Breast Cancer |
| 2026-10-01 | Ex-US | ATGGF | Actinogen Medical Limited | Phase 3 | Effect of 10 mg Xanamem on Dementia Due to Alzheimer's Disease |
| 2026-10-01 | US | BCRX | BioCryst Pharmaceuticals, Inc. | Phase 1 | A Study of the Safety, Tolerability, Pharmacokinetics, and Immunogenicity of BCX17725 |
| 2026-10-01 | US | BHVN | Biohaven Ltd. | Phase 3 | Study to Determine if BHV-7000 is Effective and Safe in Adults With Refractory Focal Onset Epilepsy |
| 2026-10-01 | Ex-US | CASBF | CanSino Biologics Inc. | Phase 2 | A Study to Evaluate the Safety and Immunogenicity of VLP-Polio in Infants and Toddlers |
| 2026-10-01 | Ex-US | CASBF | CanSino Biologics Inc. | Phase 1 | Clinical Trial of Lyophilized Haemophilus Influenzae Type b Conjugate Vaccine |
| 2026-10-01 | US | CLDX | Celldex Therapeutics, Inc. | Phase 3 | A Phase 3 Study of Barzolvolimab in Participants With Chronic Spontaneous Urticaria |
| 2026-10-01 | US | CLDX | Celldex Therapeutics, Inc. | Phase 3 | A Phase 3 Study of Barzolvolimab in Participants With Chronic Spontaneous Urticaria (CSU) |
| 2026-10-01 | US | COCP | Cocrystal Pharma, Inc. | Phase 2 | A Study to Evaluate the Efficacy, Safety and Pharmacokinetics of CDI-988 in Healthy Adults After Challenge With Snow Mountain Virus |
| 2026-10-01 | US | CORT | Corcept Therapeutics Incorporated | Phase 2 | Dazucorilant in Patients With Amyotrophic Lateral Sclerosis |
| 2026-10-01 | US | CORT | Corcept Therapeutics Incorporated | Phase 2 | Dazucorilant in Patients With Amyotrophic Lateral Sclerosis |
| 2026-10-01 | US | EYPT | EyePoint, Inc. | Phase 3 | A 2-year Study of EYP-1901 in Subjects With Wet Age Related Macular Degeneration (wAMD) (LUCIA) Primary Efficacy Will be Determined at Week 56 |
| 2026-10-01 | US | IDYA | IDEAYA Biosciences, Inc. | Phase 1 | A Study of PARG Inhibitor IDE161 in Participants With Advanced Solid Tumors |
| 2026-10-01 | US | IMCR | Immunocore Holdings plc | Phase 2 | Safety and Efficacy of IMC-F106C as a Single Agent and in Combination With Checkpoint Inhibitors |
| 2026-10-01 | Ex-US | INCPF | InnoCare Pharma Limited | Phase 2 | Efficacy and Safety of ICP-332 Versus Placebo in Participants With Moderate to Severe Plaque Psoriasis |
| 2026-10-01 | US | IOVA | Iovance Biotherapeutics, Inc. | Phase 2 | E7 T-cell Receptor (TCR) -T Cell Induction Therapy for Locoregionally Advanced HPV-associated Cancers |
| 2026-10-01 | US | IRON | Disc Medicine, Inc. | Phase 2 | Study of DISC-0974-201 in Participants With IBD and Anemia |
| 2026-10-01 | US | ITRM | Iterum Therapeutics plc | Phase 1 | Pharmacokinetics of Sulopenem Etzadroxil Plus Probenecid in Adolescents |
| 2026-10-01 | US | JANX | Janux Therapeutics, Inc. | Phase 1 | Study of JANX011 in Healthy Adult Volunteers to Assess Safety and Tolerability. |
| 2026-10-01 | US | JBIO | Jade Biosciences, Inc. | Phase 1 | A Phase 1 Study of JADE101 in Healthy Participants |
| 2026-10-01 | US | KZIA | Kazia Therapeutics Limited | Phase 2 | Genetic Testing in Guiding Treatment for Patients With Brain Metastases |
| 2026-10-01 | US | MIRM | Mirum Pharmaceuticals, Inc. | Phase 3 | Evaluation of Maralixibat in Pruritus Associated With General Cholestatic Liver Disease (EXPAND) |
| 2026-10-01 | US | NTHI | NeOnc Technologies Holdings, Inc. | Phase 1 | A Study of the Safety, Dosing, and Delivery of NEO100 in Patients With Pediatric Brain Tumors |
| 2026-10-01 | US | OGN | Organon & Co. | Phase 3 | Tapinarof for the Treatment of Plaque Psoriasis in Pediatric Subjects |
| 2026-10-01 | US | PHAR | Pharming Group N.V. | Phase 2 | Leniolisib for Immune Dysregulation in CVID |
| 2026-10-01 | US | PHAR | Pharming Group N.V. | Phase 2 | Leniolisib for Immune Dysregulation in CVID |
| 2026-10-01 | US | PHAT | Phathom Pharmaceuticals, Inc. | Phase 2 | A Study in Adult Participants With EoE to Evaluate Vonoprazan 20 mg Compared to Placebo After 12 Weeks and to Evaluate Vonoprazan 20 mg Up to 24 Weeks |
| 2026-10-01 | US | RGNX | REGENXBIO Inc. | Phase 3 | Pivotal 2 Study of RGX-314 Gene Therapy in Participants With nAMD |
| 2026-10-01 | US | RGNX | REGENXBIO Inc. | Phase 3 | Pivotal 2 Study of RGX-314 Gene Therapy in Participants With nAMD |
| 2026-10-01 | US | SNDX | Syndax Pharmaceuticals, Inc. | Phase 1 | Study of Revumenib, Azacitidine, and Venetoclax in Pediatric and Young Adult Patients With Refractory or Relapsed Acute Myeloid Leukemia |
| 2026-10-01 | US | SRNE | Sorrento Therapeutics, Inc. | Phase 1 | Study to Assess the Safety and Preliminary Efficacy of STI-1386 Oncolytic Virus in Relapsed or Refractory Solid Tumors |
| 2026-10-01 | US | TENX | Tenax Therapeutics, Inc. | Phase 3 | LEVosimendan to Improve Exercise Limitation in Patients With PH-HFpEF |
| 2026-10-01 | US | VNDA | Vanda Pharmaceuticals Inc. | Phase 2 | Evaluation of Efficacy and Safety of Iloperidone for the Treatment of Participants With Uncontrolled Hypertension |
| 2026-10-01 | US | VNDA | Vanda Pharmaceuticals Inc. | Phase 2 | Evaluation of Efficacy and Safety of Iloperidone for the Treatment of Participants With Uncontrolled Hypertension |
| 2026-10-01 | US | XENE | Xenon Pharmaceuticals Inc. | Phase 3 | A Randomized Study of XEN1101 Versus Placebo in Focal-Onset Seizures (X-TOLE3) |
| 2026-10-02 | US | FTRE | Fortrea Holdings Inc. | Phase 1 | AZD5305 hADME in Patients With Advanced Solid Malignancies |
| 2026-10-02 | US | PSTV | Plus Therapeutics, Inc. | Phase 1 | Multiple Dose Intraventricular Administration of Rhenium-186 NanoLiposome for Leptomeningeal Metastases |
| 2026-10-09 | US | TECX | Tectonic Therapeutic, Inc. | Phase 2 | A Study of TX000045 in Patients With Pulmonary Hypertension Secondary to Heart Failure With Preserved Ejection Fraction (the APEX Study) |
| 2026-10-15 | US | SLDB | Solid Biosciences Inc. | Phase 2 | Microdystrophin Gene Transfer Study in Adolescents and Children With DMD |
| 2026-10-16 | US | IOBT | IO Biotech, Inc. | Phase 2 | Neoadjuvant Pembrolizumab and IO102-103 for Squamous Cell Carcinoma of the Head and Neck (SCCHN). |
| 2026-10-24 | US | PHAR | Pharming Group N.V. | PDUFA – CRL | |
| 2026-10-30 | US | ADCT | ADC Therapeutics SA | Phase 1 | A Study to Evaluate the Safety and Anti-cancer Activity of Loncastuximab Tesirine in Combination With Other Anti-cancer Agents in Participants With Relapsed or Refractory B-cell Non-Hodgkin Lymphoma (LOTIS-7) |
| 2026-10-30 | US | INBX | Inhibrx Biosciences, Inc. | Phase 2 | Study of INBRX-106 and INBRX-106 in Combination With Pembrolizumab (Keytruda®) in Subjects With Locally Advanced or Metastatic Solid Tumors (Hexavalent OX40 Agonist) |
| 2026-10-30 | US | INO | INOVIO Pharmaceuticals, Inc. | PDUFA | |
| 2026-10-30 | US | MBX | MBX Biosciences, Inc. | Phase 1 | A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of MBX 4291 in Adult Participants With Obesity |
| 2026-10-31 | US | ADAG | Adagene Inc. | Phase 2 | ADG126 in Combination With Pembrolizumab in Patients With Advanced/Metastatic Solid Tumors |
| 2026-10-31 | US | ANNX | Annexon, Inc. | Phase 3 | A Study Investigating the Efficacy and Safety of Intravitreal (IVT) Injections of Vonaprument (Formerly ANX007) in Participants With Dry Age-Related Macular Degeneration (AMD) With Geographic Atrophy (GA) |
| 2026-10-31 | US | IMMP | Immutep Limited | Phase 3 | Study in Metastatic Breast Cancer Patients Receiving Eftilagimod Alpha or Placebo in Combination with Paclitaxel Chemotherapy |
| 2026-10-31 | US | JSPR | Jasper Therapeutics, Inc. | Phase 2 | Dose Escalation Trial Of Safety, Pharmacokinetic/Pharmacodynamic And Preliminary Clinical Activity of Briquilimab In Adult Patients With Chronic Spontaneous Urticaria (CSU) |
| 2026-10-31 | US | RCUS | Arcus Biosciences, Inc. | Phase 2 | Safety and Efficacy of Zimberelimab (AB122) in Combination With Domvanalimab (AB154) and Etrumadenant (AB928) in Patients With Previously Treated Non-Small Cell Lung Cancer |
| 2026-10-31 | US | REPL | Replimune Group, Inc. | Phase 1 | Study of RP2 Monotherapy and RP2 in Combination With Nivolumab in Patients With Solid Tumors |
| 2026-10-31 | US | SNTI | Senti Biosciences, Inc. | Phase 1 | Clinical Study of SN301A Injection in the Treatment of Hepatocellular Carcinoma |
| 2026-10-31 | US | SRPT | Sarepta Therapeutics, Inc. | Phase 3 | A Study to Compare Safety and Efficacy of High Doses of Eteplirsen in Participants With Duchenne Muscular Dystrophy (DMD) (MIS51ON) |
| 2026-10-31 | US | SYRE | Spyre Therapeutics, Inc. | Phase 2 | A Study of SPY072 in Rheumatic Disease |
| 2026-10-31 | US | TGTX | TG Therapeutics, Inc. | Phase 3 | A Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Safety, Radiological and Clinical Effects of Subcutaneous Ublituximab in Participants With Relapsing Multiple Sclerosis (RMS) |
| 2026-11-01 | US | ACIU | AC Immune SA | Phase 1 | [18F]ACI-19626 PET in TDP-43 Proteinopathies |
| 2026-11-01 | US | ANL | Adlai Nortye Ltd. | Phase 1 | First in Human, Dose Escalation Study of AN4005 |
| 2026-11-01 | US | APGE | Apogee Therapeutics, Inc. | Phase 2 | A Study Evaluating APG777 in Atopic Dermatitis |
| 2026-11-01 | Ex-US | APTOF | Aptose Biosciences Inc. | Phase 2 | Clinical Trial to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Tuspetinib (HM43239) in Patients With Relapsed or Refractory Acute Myeloid Leukemia |
| 2026-11-01 | US | ATOS | Atossa Therapeutics, Inc. | Phase 2 | (Z)-Endoxifen for the Treatment of Premenopausal Women With ER+/HER2- Breast Cancer |
| 2026-11-01 | US | BHVN | Biohaven Ltd. | Phase 1 | A Phase 1b Study of BHV-7000 in Participants With Inherited Erythromelalgia |
| 2026-11-01 | US | BRNS | Barinthus Biotherapeutics plc | Phase 1 | VTP-1000 in Adults With Celiac Disease |
| 2026-11-01 | US | BYSI | BeyondSpring Inc. | Phase 2 | Study of Plinabulin and Pegfilgrastim in People With Multiple Myeloma Undergoing an Autologous Hematopoietic Stem Cell Transplant (AHCT) |
| 2026-11-01 | US | CGEM | Cullinan Therapeutics, Inc. | Phase 1 | A Study of CLN-978 in Patients With Relapsed or Refractory (R/R) B Cell Non-Hodgkin Lymphoma (B-NHL) |
| 2026-11-01 | US | CGON | CG Oncology, Inc. | Phase 3 | A Study of Adjuvant Cretostimogene Grenadenorepvec for Treatment of Intermediate Risk NMIBC Following TURBT |
| 2026-11-01 | Ex-US | CHIZF | China Traditional Chinese Medicine Holdings Co. Limited | Phase 2 | Orelabrutinib in Combination with R-CHOP for CD5-positive DLBCL Patients(Rocket Trial) |
| 2026-11-01 | Ex-US | CHIZF | China Traditional Chinese Medicine Holdings Co. Limited | Phase 1 | The Dosing Regimen of Pyrotinib in HER2-positive Advanced First-line Breast Cancer: a Phase I Clinical Study |
| 2026-11-01 | US | CRBP | Corbus Pharmaceuticals Holdings, Inc. | Phase 2 | First-in-human Study of CRB-601-01 to Treat Patients With Advanced Solid Tumor. |
| 2026-11-01 | US | CRDF | Cardiff Oncology, Inc. | Phase 2 | Study of Onvansertib in Combination With FOLFIRI and Bevacizumab or FOLFOX and Bevacizumab Versus FOLFIRI and Bevacizumab or FOLFOX and Bevacizumab for First-Line Treatment of Metastatic Colorectal Cancer in Adult Participants With a KRAS or NRAS Mutation |
| 2026-11-01 | US | DBVT | DBV Technologies S.A. | Phase 3 | Safety Study of Viaskin® Peanut Patch in Peanut-Allergic Children 1 Through 3 Years of Age (COMFORT Toddlers) |
| 2026-11-01 | US | DRUG | Bright Minds Biosciences Inc. | Phase 2 | A 2-Part Study to Assess Efficacy, Safety and Tolerability of BMB-101 for the Treatment of Patients With Prader-Willi Syndrome. |
| 2026-11-01 | US | ELTX | Elicio Therapeutics, Inc. | Phase 2 | A Study of ELI-002 7P in Subjects With KRAS/NRAS Mutated Solid Tumors |
| 2026-11-01 | US | HRMY | Harmony Biosciences Holdings, Inc. | Phase 3 | An Efficacy and Safety Study of Clemizole HCl in Patients With Lennox-Gastaut Syndrome |
| 2026-11-01 | US | IMUX | Immunic, Inc. | Phase 3 | Study to Evaluate the Efficacy, Safety, and Tolerability of IMU-838 in Patients With Relapsing Multiple Sclerosis |
| 2026-11-01 | US | IOVA | Iovance Biotherapeutics, Inc. | Phase 1 | A Study of LN-144 in People With Metastatic Melanoma to the Brain |
| 2026-11-01 | US | KPRX | Kiora Pharmaceuticals, Inc. | Phase 2 | Safety, Tolerability and Efficacy of Intravitreal KIO-104 in Patients With Macular Edema |
| 2026-11-01 | Ex-US | MCUJF | Medicure Inc. | Phase 3 | Oral Pyridoxal 5'-Phosphate for the Treatment of Patients With PNPO Deficiency |
| 2026-11-01 | US | MGNX | MacroGenics, Inc. | Phase 1 | A Study of MGD024 in Patients With Relapsed or Refractory Hematologic Malignancies |
| 2026-11-01 | US | MGNX | MacroGenics, Inc. | Phase 1 | A Study of MGC028 in Participants With Advanced Solid Tumors |
| 2026-11-01 | US | NAMS | NewAmsterdam Pharma Company N.V. | Phase 3 | Cardiovascular Outcome Study to Evaluate the Effect of Obicetrapib in Patients With Cardiovascular Disease |
| 2026-11-01 | US | RCUS | Arcus Biosciences, Inc. | Phase 1 | A Study of AB801 Monotherapy and Combination Therapy in Participants With Advanced Malignancies |
| 2026-11-01 | US | SRRK | Scholar Rock Holding Corporation | Phase 3 | Long-Term Safety & Efficacy of Apitegromab in Patients With SMA Who Completed Previous Trials of Apitegromab |
| 2026-11-01 | US | STJO | St. Joseph, Inc. | Phase 2 | Trial Evaluating 3-year Disease Free Survival in Patients With Locally Advanced Rectal Cancer Treated With Chemoradiation Plus Induction or Consolidation Chemotherapy and Total Mesorectal Excision or Non-operative Management |
| 2026-11-01 | US | TLX | Telix Pharmaceuticals Limited | Phase 1 | PSMA PET Response Guided SabR in High Risk Pca |
| 2026-11-01 | US | TYRA | Tyra Biosciences, Inc. | Phase 2 | Safety and Preliminary Anti-Tumor Activity of TYRA-300 in Advanced Urothelial Carcinoma and Other Solid Tumors With FGFR3 Gene Alterations |
| 2026-11-01 | US | VIR | Vir Biotechnology, Inc. | Phase 2 | A Study to Evaluate Tobevibart+Elebsiran Versus Bulevirtide in Chronic HDV Infection |
| 2026-11-01 | US | ZURA | Zura Bio Limited | Phase 2 | Tibulizumab Skin Healing and Inflammation Evaluation for Lasting Defense |
| 2026-11-18 | US | SYRE | Spyre Therapeutics, Inc. | Phase 1 | A Study of SPY003-207 in Healthy Volunteers |
| 2026-11-20 | US | SKYE | Skye Bioscience, Inc. | Phase 2 | Study to Evaluate the Effect on Obesity of QW Nimacimab and QW Nimacimab Co-administered With Semaglutide vs Placebo |
| 2026-11-22 | Ex-US | RVXCF | Resverlogix Corp. | Phase 2 | A Two-Part Phase 2a Study of RVX000222 in Patients With End-Stage Renal Disease Treated With Hemodialysis |
| 2026-11-24 | Ex-US | CASBF | CanSino Biologics Inc. | Phase 2 | Clinical Trial of the 24-valent Pneumococcal Polysaccharide Conjugate Vaccine (CRM197/Tetanus Toxoid) |
| 2026-11-25 | Ex-US | INCPF | InnoCare Pharma Limited | Phase 3 | ICP-332 in Subjects With Moderate to Severe Atopic Dermatitis |
| 2026-11-30 | US | AURA | Aura Biosciences, Inc. | Phase 2 | Suprachoroidal Administration in Subjects With Metastases to the Choroid |
| 2026-11-30 | US | BIOA | BioAge Labs, Inc. | Phase 2 | A Phase 2 Study to Evaluate the Pharmacodynamics, Safety and Tolerability of BGE-102 in Participants With Obesity and Cardiovascular Risk Factors |
| 2026-11-30 | Ex-US | BVNRY | Bavarian Nordic A/S | Phase 2 | Comparability Trial of the MVA-BN Vaccine Manufactured in Different Production Cells |
| 2026-11-30 | US | IMCR | Immunocore Holdings plc | Phase 2 | Phase 1/2 Study of IMC-R117C in Selected Advanced Cancers |
| 2026-11-30 | US | QURE | uniQure N.V. | Phase 2 | AMT-260 Gene Therapy Study in Adults With Unilateral Refractory Mesial Temporal Lobe Epilepsy |
| 2026-11-30 | US | REPL | Replimune Group, Inc. | Phase 1 | Study of RP3 Monotherapy and RP3 in Combination With Nivolumab in Patients With Solid Tumours |
| 2026-11-30 | US | RNAC | Cartesian Therapeutics, Inc. | Phase 3 | Investigating an mRNA CAR T-cell Therapy, Known as Descartes-08, as a Potential Approach to Treat Myasthenia Gravis |
| 2026-12-01 | US | ABUS | Arbutus Biopharma Corporation | Phase 2 | Intrahepatic and Peripheral Responses to Imdusiran (AB-729) in Chronic Hepatitis B |
| 2026-12-01 | US | ACLX | Arcellx, Inc. | Phase 2 | Study of Anitocabtagene-autoleucel in Relapsed or Refractory Multiple Myeloma (iMMagine-1) |
| 2026-12-01 | US | ADCT | ADC Therapeutics SA | Phase 1 | A Study to Evaluate the Pharmacokinetics and Safety of Loncastuximab Tesirine in Participants With Relapsed or Refractory Diffuse Large B-cell Lymphoma or High-grade B-cell Lymphoma With Hepatic Impairment (LOTIS-10) |
| 2026-12-01 | US | AGEN | Agenus Inc. | Phase 2 | Vorbipiprant (CR6086) / Balstilimab (AGEN2034) Combination in Stage IV Refractory pMMR – MSS CRC, and Other Metastatic GI Cancers |
| 2026-12-01 | US | AGEN | Agenus Inc. | Phase 2 | Platform Study of Immunotherapy Combinations in Colorectal Cancer Liver Metastases |
| 2026-12-01 | US | ALDX | ALDEYRA THERAPEUTICS, INC. | Phase 3 | A Clinical Trial Evaluating Patients With Primary Vitreoretinal Lymphoma |
| 2026-12-01 | US | ALMS | Alumis Inc. | Phase 2 | Open-Label Extension Study to Evaluate the Long Term Safety and Efficacy of ESK-001 in Plaque Psoriasis |
| 2026-12-01 | US | ANRO | Alto Neuroscience, Inc. | Phase 2 | Study of ALTO-300 in MDD |
| 2026-12-01 | US | ARDX | Ardelyx, Inc. | Phase 2 | Tenapanor in Synucleinopathy-Related Constipation |
| 2026-12-01 | US | ATXS | Astria Therapeutics, Inc. | Phase 3 | A Study of Navenibart in Participants With Hereditary Angioedema |
| 2026-12-01 | US | AVIR | Atea Pharmaceuticals, Inc. | Phase 3 | C-Forward: Efficacy and Safety of BEM/RZR vs SOF/VEL in Subjects With Chronic HCV |
| 2026-12-01 | US | BCDA | BioCardia, Inc. | Phase 2 | Clinical Trial of Human Allogenic Culture-expanded Bone Marrow-derived Mesenchymal Stem Cells |
| 2026-12-01 | US | BEAM | Beam Therapeutics Inc. | Phase 2 | A Study Evaluating the Safety and Efficacy of BEAM-201 in Relapsed/Refractory T-Cell Acute Lymphoblastic Leukemia (T-ALL) or T-Cell Lymphoblastic Lymphoma (T-LL) |
| 2026-12-01 | US | BHVN | Biohaven Ltd. | Phase 3 | A Study to Determine if BHV-7000 is Effective and Safe in Adults With Refractory Focal Onset Epilepsy |
| 2026-12-01 | US | BHVN | Biohaven Ltd. | Phase 2 | Long-term Safety and Tolerability of BHV-7000 |
| 2026-12-01 | Ex-US | BRIBF | Brii Biosciences Limited | Phase 2 | Study to Investigate the Efficacy and Safety of Regimens Containing BRII-179, BRII-835, and PEG-IFNα Treating Chronic Hepatitis B Virus (HBV) Infection (ENRICH) |
| 2026-12-01 | US | BRTX | BioRestorative Therapies, Inc. | Phase 2 | A Single Dose of BRTX 100 for Patients With Chronic Lumbar Disc Disease (cLDD) |
| 2026-12-01 | US | CGEM | Cullinan Therapeutics, Inc. | Phase 1 | A Study of CLN-978, a Subcutaneously Administered CD19-directed T Cell Engager, in Subjects With Systemic Lupus Erythematosus |
| 2026-12-01 | US | CMPX | Compass Therapeutics, Inc. | Phase 1 | A Phase 1 of CTX-8371 in Patients With Advanced Malignancies |
| 2026-12-01 | US | CNTA | Centessa Pharmaceuticals plc | Phase 2 | A Study of ORX750 in Participants With Narcolepsy and Idiopathic Hypersomnia |
| 2026-12-01 | US | CNTX | Context Therapeutics Inc. | Phase 1 | CT-95 in Advanced Cancers Associated With Mesothelin Expression |
| 2026-12-01 | US | DCTH | Delcath Systems, Inc. | Phase 2 | Evaluation of the Safety and Efficacy of Treatment w/High Dose Melphalan Given Directly Into the Liver Followed by Treatment w/Approved Cancer Treatment or Approved Cancer Treatment Alone in Patients w/ Metastatic Colorectal Cancer w/Liver Dominant Disease |
| 2026-12-01 | US | DMAC | DiaMedica Therapeutics Inc. | Phase 3 | Treatment of Acute Ischemic Stroke (ReMEDy2 Trial) |
| 2026-12-01 | US | DNLI | Denali Therapeutics Inc. | Phase 2 | A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of DNL593 in Healthy Participants and Participants With Frontotemporal Dementia (FTD-GRN) |
| 2026-12-01 | US | DSGN | Design Therapeutics, Inc. | Phase 2 | A Multiple Ascending Dose Study of DT-216P2 in Patients With Friedreich's Ataxia |
| 2026-12-01 | US | EIKN | Eikon Therapeutics, Inc. | Phase 2 | A Phase 2 Study of EIK1001 in Combo With Pembrolizumab and Chemotherapy in Patients With Stage 4 NSCLC |
| 2026-12-01 | US | EPRX | Eupraxia Pharmaceuticals Inc. | Phase 2 | A Trial to Evaluate EP-104GI in Adults With Eosinophilic Esophagitis (EoE). |
| 2026-12-01 | US | GLSI | Greenwich LifeSciences, Inc. | Phase 3 | Phase 3 Study to Evaluate the Efficacy and Safety of HER2/Neu Peptide GLSI-100 (GP2 + GM-CSF) in HER2/Neu Positive Subjects |
| 2026-12-01 | US | GNLX | Genelux Corporation | Phase 2 | Olvi-Vec Combined With Platinum Plus Etoposide Therapy in Patients With Late Phase SCLC |
| 2026-12-01 | US | GOSS | Gossamer Bio, Inc. | Phase 3 | Open-label Extension Study of Seralutinib in Adult Subjects With PAH (PROSERA-EXT) |
| 2026-12-01 | US | IMMX | Immix Biopharma, Inc. | Phase 2 | Study of NXC-201 CAR-T in Patients With Light Chain (AL) Amyloidosis |
| 2026-12-01 | US | IXHL | Incannex Healthcare Inc. | Phase 3 | RePOSA-Revealing the Efficacy of IHL-42X Use in Patients With OSA |
| 2026-12-01 | US | KPTI | Karyopharm Therapeutics Inc. | Phase 2 | Selinexor (KPT-330) in Patients With Relapsed/Refractory Diffuse Large B-Cell Lymphoma (DLBCL) |
| 2026-12-01 | US | KPTI | Karyopharm Therapeutics Inc. | Phase 3 | A Study of Rituximab-Gemcitabine-Dexamethasone-Platinum (R-GDP) With or Without Selinexor in Patients With Relapsed/Refractory Diffuse Large B-cell Lymphoma |
| 2026-12-01 | US | KZIA | Kazia Therapeutics Limited | Phase 1 | GDC-0084 With Radiation Therapy for People With PIK3CA-Mutated Solid Tumor Brain Metastases or Leptomeningeal Metastases |
| 2026-12-01 | US | KZIA | Kazia Therapeutics Limited | Phase 2 | Paxalisib (GDC-0084) In Recurrent Or Refractory PCNSL |
| 2026-12-01 | US | LXEO | Lexeo Therapeutics, Inc. | Phase 2 | Gene Therapy for ACM Due to a PKP2 Pathogenic Variant |
| 2026-12-01 | US | MDWD | MediWound Ltd. | Phase 3 | A Double Blind Study Performed to Evaluate the Efficacy and the Safety of EscharEx in Debridement of VLU (VALUE) |
| 2026-12-01 | US | MGTX | MeiraGTx Holdings plc | Phase 2 | A Study of AAV2-hAQP1 Gene Therapy in Participants With Radiation-Induced Late Xerostomia |
| 2026-12-01 | US | MNPR | Monopar Therapeutics Inc. | Phase 1 | Dose-Escalation of MNPR-101-PCTA-177Lu in Solid Tumors |
| 2026-12-01 | Ex-US | NPPNY | Nippon Shinyaku Co., Ltd. | Phase 2 | Trial of Efficacy and Safety of NS-229 Versus Placebo in Patients With Eosinophilic Granulomatosis With Polyangiitis |
| 2026-12-01 | US | NVCT | Nuvectis Pharma, Inc. | Phase 1 | Study of NXP900 With Osimertinib in Subjects With Advanced, EGFR-Mutated Non-Small Cell Lung Cancer |
| 2026-12-01 | US | NXTC | NextCure, Inc. | Phase 1 | A Phase 1 Study of LNCB74 in Advanced Solid Tumors |
| 2026-12-01 | US | OMER | Omeros Corporation | Phase 2 | Long-Term Safety, Tolerability and Efficacy of OMS906 in Paroxysmal Nocturnal Hemoglobinuria |
| 2026-12-01 | US | ORIC | ORIC Pharmaceuticals, Inc. | Phase 1 | ORIC-114 in Combination With Subcutaneous Amivantamab in Patients With EGFR Exon20 Insertion Mutant NSCLC |
| 2026-12-01 | US | PBYI | Puma Biotechnology, Inc. | Phase 2 | Capecitabine 7/7 Schedule With Neratinib in Patients With Metastatic HER2-Positive Breast Cancer |
| 2026-12-01 | US | PMN | ProMIS Neurosciences, Inc. | Phase 1 | PMN310 in Patients With Early Alzheimer's Disease (PRECISE-AD) |
| 2026-12-01 | US | PRAX | Praxis Precision Medicines, Inc. | Phase 3 | A Clinical Trial for Participants With DEE to Assess Efficacy, Safety, Tolerability, and PK of Relutrigine |
| 2026-12-01 | US | RANI | Rani Therapeutics Holdings, Inc. | Phase 1 | An Early Phase Study of RT-114 (RaniPill Containing PG-102, a GLP-1/2 Dual Agonist) in Healthy Volunteers. |
| 2026-12-01 | US | RCUS | Arcus Biosciences, Inc. | Phase 2 | A Phase I-II Study to Test the Safety and Efficacy of PD1 (AB122) and Adenosine Receptor (AB928) Antagonists With Chemotherapy After Short-Course Radiation for Rectal Cancer. |
| 2026-12-01 | US | RCUS | Arcus Biosciences, Inc. | Phase 2 | Zimberelimab and Quemliclustat in Combination With Chemotherapy for the Treatment of Patients With Borderline Resectable and Locally Advanced Pancreatic Adenocarcinoma |
| 2026-12-01 | US | RCUS | Arcus Biosciences, Inc. | Phase 2 | Adenosine Signaling Modulation and Immune Checkpoint Inhibition With Hormone Sensitive Oligometastatic Prostate Cancer |
| 2026-12-01 | US | RCUS | Arcus Biosciences, Inc. | Phase 1 | A Study to Investigate the Safety, Tolerability, and PK of AB102 in Healthy Participants |
| 2026-12-01 | US | RGNX | REGENXBIO Inc. | Phase 3 | Pivotal 1 Study of ABBV-RGX-314 (Also Known as RGX-314) Gene Therapy Administered Via Subretinal Delivery One Time in Participants With nAMD |
| 2026-12-01 | US | SNDX | Syndax Pharmaceuticals, Inc. | Phase 2 | A Phase I-II Study Investigating the All-Oral Combination of the Menin Inhibitor SNDX-5613 With Decitabine/Cedazuridine (ASTX727) and Venetoclax in Acute Myeloid Leukemia (SAVE) |
| 2026-12-01 | US | SNDX | Syndax Pharmaceuticals, Inc. | Phase 2 | A Phase II Study of the Menin Inhibitor Revumenib in Leukemia Associated With Upregulation of HOX Genes |
| 2026-12-01 | Ex-US | TLTFF | Theralase Technologies Inc. | Phase 2 | Intravesical Photodynamic Therapy ("PDT") in BCG-Unresponsive/Intolerant Non-Muscle Invasive Bladder Cancer ("NMIBC") Patients |
| 2026-12-01 | US | TVTX | Travere Therapeutics, Inc. | Phase 1 | Sparsentan for the Treatment of VEGF Signaling Pathway Inhibitor-Associated Proteinuria |
| 2026-12-01 | US | VIR | Vir Biotechnology, Inc. | Phase 2 | Study to Investigate the Efficacy and Safety of Regimens Containing BRII-179, BRII-835, and PEG-IFNα Treating Chronic Hepatitis B Virus (HBV) Infection (ENRICH) |
| 2026-12-01 | US | VIR | Vir Biotechnology, Inc. | Phase 3 | A Study to Evaluate Tobevibart+Elebsiran in Participants With Chronic HDV Infection Not Virologically Suppressed With Bulevirtide |
| 2026-12-01 | US | VNDA | Vanda Pharmaceuticals Inc. | Phase 3 | Study to Evaluate the Efficacy and Safety of VQW-765 for the On-Demand Treatment of Social Anxiety Disorder |
| 2026-12-01 | US | VNDA | Vanda Pharmaceuticals Inc. | Phase 3 | Study to Evaluate the Efficacy and Safety of VQW-765 for the On-Demand Treatment of Social Anxiety Disorder |
| 2026-12-01 | US | ZNTL | Zentalis Pharmaceuticals, Inc. | Phase 2 | A Study of Azenosertib (ZN-c3) in Subjects With Platinum-Resistant High-Grade Serous Ovarian, Fallopian Tube or Primary Peritoneal Cancer |
| 2026-12-01 | US | ZYME | Zymeworks Inc. | Phase 1 | A Study of ZW191 in Participants With Solid Tumors |
| 2026-12-02 | US | XNCR | Xencor, Inc. | Phase 2 | XmAb20717 in Advanced Biliary Tract Cancers |
| 2026-12-03 | US | VSTM | Verastem, Inc. | Phase 1 | Identification of Treatment Concentrations of Defactinib or VS-6766 for the Treatment of Patients With Glioblastoma |
| 2026-12-04 | US | ARVN | Arvinas, Inc. | Phase 1 | A Study to Learn How the Body Processes the Study Medicine Called Vepdegestrant in People With Loss of Liver Function |
| 2026-12-15 | US | CRDF | Cardiff Oncology, Inc. | Phase 2 | Onvansertib + Paclitaxel In TNBC |
| 2026-12-15 | Ex-US | GEDSF | Gedeon Richter PLC | Phase 3 | Efficacy and Safety of Cariprazine in the Treatment of Adolescent Participants (13 to 17 Years of Age) With Schizophrenia |
| 2026-12-22 | US | ENSC | Ensysce Biosciences, Inc. | Phase 1 | Single Dose Study, Pharmacokinetics of Oxycodone and PF614 Co-Administered With Nafamostat (PF614-MPAR-102) |
| 2026-12-28 | Ex-US | INCPF | InnoCare Pharma Limited | Phase 2 | A Phase I/II Study of CM355 in Patients With Relapsed or Refractory B-Cell Non-Hodgkin's Lymphoma (B-NHL) |
| 2026-12-30 | US | ARVN | Arvinas, Inc. | Phase 2 | TACTIVE-U: A Study to Learn About the Study Medicine (Vepdegestrant) When Given With Other Medicines in People With Advanced or Metastatic Breast Cancer (Sub-Study B) |
| 2026-12-30 | US | ARVN | Arvinas, Inc. | Phase 3 | Vepdegestrant (ARV-471/PF-07850327) + Palbociclib vs Letrozole + Palbociclib in ER(+)/HER2(-) Advanced Breast Cancer |
| 2026-12-30 | US | ARVN | Arvinas, Inc. | Phase 3 | Vepdegestrant (ARV-471/PF-07850327) + Palbociclib vs Letrozole + Palbociclib in ER(+)/HER2(-) Advanced Breast Cancer |
| 2026-12-30 | US | HOTH | Hoth Therapeutics, Inc. | Phase 2 | Study to Investigate the Efficacy, Safety, and Tolerability of Topical HT-001 for the Treatment of Skin Toxicities Associated With Epidermal Growth Factor Receptor Inhibitors |
| 2026-12-30 | US | IMCR | Immunocore Holdings plc | Phase 2 | Tebentafusp in Molecular Relapsed Disease (MRD) Melanoma |
| 2026-12-30 | US | NTHI | NeOnc Technologies Holdings, Inc. | Phase 2 | NEO100 and High-Grade Meningioma |
| 2026-12-30 | Ex-US | PSYGF | Psyence Group Inc. | Phase 2 | Psilocybin-Assisted Psychotherapy in Cancer Patients With Adjustment Disorder |
| 2026-12-30 | US | SNDX | Syndax Pharmaceuticals, Inc. | Phase 2 | A Multi-Site Break Through Cancer Trial: Phase II Study Investigating Dual Inhibition of BCL2 and Menin in AML MRD Using the Combination of Venetoclax and Revumenib |
| 2026-12-30 | US | SUPN | Supernus Pharmaceuticals, Inc. | Phase 2 | BIS-001-ER for the Treatment of Adult Focal Impaired Awareness Seizures |
| 2026-12-30 | US | TCRX | TScan Therapeutics, Inc. | Phase 1 | A Basket Study of Customized Autologous TCR-T Cell Therapies in Patients With Locally Advanced (Unresectable) or Metastatic Solid Tumors |
| 2026-12-31 | US | ACAD | ACADIA Pharmaceuticals Inc. | Phase 2 | Pimavanserin for Rigid-compulsive Symptoms in Autism Spectrum Disorder |
| 2026-12-31 | US | ADAG | Adagene Inc. | Phase 2 | Pembrolizumab and ADG106 in Advanced Solid Cancers and Triple Negative Breast Cancer |
| 2026-12-31 | US | ADCT | ADC Therapeutics SA | Phase 1 | Addition of Loncastuximab Tesirine to Acalbrutinib , Chronic Lymphocytic Leukemia |
| 2026-12-31 | US | ANNX | Annexon, Inc. | Phase 3 | An Open Label Clinical Study to Evaluate Tanruprubart (Also Commonly Known as ANX005) in Participants With Guillain-Barré Syndrome (FORWARD Study) |
| 2026-12-31 | US | ARVN | Arvinas, Inc. | Phase 2 | TACTIVE-U: A Study to Learn About the Study Medicine (Vepdegestrant) When Given With Other Medicines in People With Advanced or Metastatic Breast Cancer. (Sub-Study C) |
| 2026-12-31 | US | BCAX | Bicara Therapeutics Inc. | Phase 1 | Study of Safety and Tolerability of BCA101 Monotherapy and in Combination Therapy in Patients With EGFR-driven Advanced Solid Tumors |
| 2026-12-31 | US | CATX | Perspective Therapeutics, Inc. | Phase 1 | A Safety Study of 212Pb-VMT-alpha-NET in Patients With Neuroendocrine Tumors |
| 2026-12-31 | Ex-US | CHIZF | China Traditional Chinese Medicine Holdings Co. Limited | Phase 3 | The Efficacy and Safety of Dapagliflozin in the Treatment of Hereditary Kidney Disease With Proteinuria in Children |
| 2026-12-31 | Ex-US | CLRPF | Clarity Pharmaceuticals Ltd | Phase 3 | 64Cu-SAR-bisPSMA Positron Emission Tomography: A Phase 3 Study of Participants With Biochemical Recurrence of Prostate Cancer |
| 2026-12-31 | Ex-US | CRTHF | CARsgen Therapeutics Holdings Limited | Phase 1 | A Study to Evaluate the Efficacy and Safety of CT041 After Adjuvant Chemotherapy for Pancreatic Cancer |
| 2026-12-31 | Ex-US | CRTHF | CARsgen Therapeutics Holdings Limited | Phase 1 | CT011 Autologous CAR-T Cells in Patients With Hepatocellular Carcinoma at Risk of Recurrence After Surgical Resection |
| 2026-12-31 | Ex-US | CRTHF | CARsgen Therapeutics Holdings Limited | Phase 1 | CT1190B in the Treatment of Patients With Moderate to Severe Refractory Systemic Lupus Erythematosus (SLE) or Refractory/Progressive Systemic Sclerosis (SSc) |
| 2026-12-31 | Ex-US | CRTHF | CARsgen Therapeutics Holdings Limited | Phase 1 | Safety, Efficacy and Cellular Metabolic Dynamics of ct1192 in Patients With Moderate to Severe Refractory SLE |
| 2026-12-31 | Ex-US | CRTHF | CARsgen Therapeutics Holdings Limited | Phase 1 | The Safety, Efficacy, and Cellular Metabolic Kinetics of CT1192 in Treating Patients With Anti Neutrophil Cytoplasmic Antibody Associated Vasculitis |
| 2026-12-31 | US | ESLA | Estrella Immunopharma, Inc. | Phase 2 | T-Cell Therapy (EB103) in Adults With Relapsed/Refractory B-Cell Non-Hodgkin's Lymphoma (NHL) |
| 2026-12-31 | US | FBRX | Forte Biosciences, Inc. | Phase 1 | A Study to Evaluate the Safety and Efficacy of FB102 in Patients With Non-segmental Vitiligo |
| 2026-12-31 | US | FOLD | Amicus Therapeutics, Inc. | Phase 3 | A Study to Evaluate Migalastat in Fabry Subjects With Amenable GLA Variant and Renal Disease |
| 2026-12-31 | US | GOVX | GeoVax Labs, Inc. | Phase 2 | SARS-CoV-2 Vaccine (GEO-CM04S1) Versus mRNA SARS-COV-2 Vaccine in Patients With Blood Cancer |
| 2026-12-31 | US | INO | Inovio Pharmaceuticals, Inc. | Phase 2 | INO-5401 and INO-9012 Delivered by Electroporation (EP) in Combination With Cemiplimab (REGN2810) in Newly-Diagnosed Glioblastoma (GBM) |
| 2026-12-31 | Ex-US | JCRRF | JCR Pharmaceuticals Co., Ltd. | Phase 2 | An Extension Study of JR-141-BR21 in Patients With Mucopolysaccharidosis II |
| 2026-12-31 | Ex-US | MRCHF | H.U. Group Holdings, Inc. | Phase 1 | Effect of Minimally Invasive Surgical Assisted by Robots on Intraventricular Hemorrhage |
| 2026-12-31 | US | PBYI | Puma Biotechnology, Inc. | Phase 1 | Alisertib in Combination With Osimertinib in Metastatic EGFR-mutant Lung Cancer |
| 2026-12-31 | US | PHIO | Phio Pharmaceuticals Corp. | Phase 1 | Adoptive Cell Therapy Using Cancer Specific CD8+ Tumor Infiltrating Lymphocytes in Adult Patients With Solid Tumors |
| 2026-12-31 | US | STJO | St. Joseph, Inc. | Phase 1 | Adoptive Cell Therapy Using Cancer Specific CD8+ Tumor Infiltrating Lymphocytes in Adult Patients With Solid Tumors |
| 2026-12-31 | US | SUPN | Supernus Pharmaceuticals, Inc. | Phase 2 | Double-blind, Placebo-controlled Study in Adults With Major Depressive Disorder |
| 2026-12-31 | US | VIR | Vir Biotechnology, Inc. | Phase 3 | A Study to Evaluate Tobevibart + Elebsiran in Chronic HDV Infection |
| 2026-12-31 | Ex-US | ZLDPF | Zealand Pharma A/S | Phase 3 | Enzalutamide in First Line Androgen Deprivation Therapy for Metastatic Prostate Cancer |
| 2027-01-01 | US | ACAD | ACADIA Pharmaceuticals Inc. | Phase 2 | Pimavanserin and Aggression and Social Cognition. |
| 2027-01-01 | US | AGEN | Agenus Inc. | Phase 1 | Botensilimab, Balstilimab, and SBRT in Colorectal Cancer |
| 2027-01-01 | Ex-US | ASPHF | Ascentage Pharma Group International | Phase 1 | A Phase I Study of Decitabine, Lisaftoclax, and Olverembatinib in Patients With Advanced Chronic Myeloid Leukemia and Philadelphia Chromosome-Positive Acute Myeloid Leukemia |
| 2027-01-01 | US | CALC | CalciMedica, Inc. | Phase 2 | Study of CM4620 to Reduce the Severity of Pancreatitis Due to Asparaginase |
| 2027-01-01 | US | CGEM | Cullinan Therapeutics, Inc. | Phase 1 | CLN-049 in Patients With Relapsed/Refractory Acute Myeloid Leukemia (AML) or Myelodysplastic Syndrome (MDS) |
| 2027-01-01 | US | COYA | Coya Therapeutics, Inc. | Phase 2 | Study of COYA 302 for the Treatment of ALS |
| 2027-01-01 | Ex-US | CSPHF | CStone Pharmaceuticals | Phase 2 | A Phase I/II Study of CS2009 in Participants With Advanced Solid Tumors |
| 2027-01-01 | US | ELDN | Eledon Pharmaceuticals, Inc. | Phase 2 | Safety, Pharmacokinetics, and Efficacy of AT 1501 in Patients Undergoing Kidney Transplant |
| 2027-01-01 | US | ELVN | Enliven Therapeutics, Inc. | Phase 1 | ELVN-002 With Trastuzumab +/- Chemotherapy in HER2+ Solid Tumors, Colorectal and Breast Cancer |
| 2027-01-01 | US | EWTX | Edgewise Therapeutics, Inc. | Phase 2 | A Study of EDG-5506 in Children With Duchenne Muscular Dystrophy (LYNX) |
| 2027-01-01 | Ex-US | HOPHF | Hemogenyx Pharmaceuticals Plc | Phase 1 | Clinical Study of Anti-FLT3 CAR-T Cells for the Treatment of Relapsed/Refractory AML |
| 2027-01-01 | US | IOVA | Iovance Biotherapeutics, Inc. | Phase 2 | E7 TCR-T Cell Immunotherapy for Human Papillomavirus (HPV) Associated Cancers |
| 2027-01-01 | Ex-US | JBPHF | Jacobio Pharmaceuticals Group Co., Ltd. | Phase 2 | JAB-30355 in Patients With Advanced Solid Tumors Harboring TP53 Y220C Mutation |
| 2027-01-01 | US | KURA | Kura Oncology, Inc. | Phase 1 | KO-2806 Monotherapy and Combination Therapies in Advanced Solid Tumors |
| 2027-01-01 | US | KURA | Kura Oncology, Inc. | Phase 1 | Ziftomenib in Combination With Chemotherapy for Children With Relapsed/Refractory Acute Leukemia |
| 2027-01-01 | US | KYTX | Kyverna Therapeutics, Inc. | Phase 2 | Anti-CD 19 CAR-T Cell Therapy in Patients With ANCA Vasculitis |
| 2027-01-01 | US | LRMR | Larimar Therapeutics, Inc. | Phase 2 | An Open-Label Study of CTI-1601 in Subjects With Friedreich's Ataxia |
| 2027-01-01 | US | NRIX | Nurix Therapeutics, Inc. | Phase 1 | A Study of NX-5948 in Adults With Relapsed/Refractory B-cell Malignancies |
| 2027-01-01 | US | ORKA | Oruka Therapeutics, Inc. | Phase 1 | ORKA-002-211 A Phase I Study to Evaluate ORKA-002 in Healthy Volunteers Following A Single Dose |
| 2027-01-01 | US | PYPD | PolyPid Ltd. | PDUFA | |
| 2027-01-01 | US | RARE | Ultragenyx Pharmaceutical Inc. | Phase 3 | Setrusumab in Pediatric Japanese Subjects With Osteogenesis Imperfecta |
| 2027-01-01 | US | RCUS | Arcus Biosciences, Inc. | Phase 2 | A Safety and Efficacy Study of Treatment Combinations With and Without Chemotherapy in Adult Participants With Advanced Upper Gastrointestinal Tract Malignancies |
| 2027-01-01 | US | REPL | Replimune Group, Inc. | Phase 2 | Phase II Study of RP2 as Immunoprevention in High-Risk Oral Precancerous Disease |
| 2027-01-01 | US | REPL | Replimune Group, Inc. | Phase 2 | Phase II Study of RP2 as Immunoprevention in High-Risk Oral Precancerous Disease |
| 2027-01-01 | US | SGMT | Sagimet Biosciences Inc. | Phase 1 | Phase 1 Study to Evaluate the Safety, Tolerability, PK, and PD of TVB-3567 in Healthy Participants With or Without Acne |
| 2027-01-01 | US | XENE | Xenon Pharmaceuticals Inc. | Phase 3 | An Open-Label Study of Azetukalner in Major Depressive Disorder |
| 2027-01-01 | US | ZVRA | Zevra Therapeutics, Inc. | Phase 2 | Study of Sodium Phenylbutyrate (ACER-001) for the Treatment of Pediatric and Adults Patients With Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCADD) |
| 2027-01-03 | Ex-US | CRTHF | CARsgen Therapeutics Holdings Limited | Phase 1 | a Study of CT0596 in Relapsed/Refractory Multiple Myeloma and Relapsed/Refractory Plasma Cell Leukemia |
| 2027-01-03 | Ex-US | CRTHF | CARsgen Therapeutics Holdings Limited | Phase 1 | A Study of CT0596 in Relapsed/Refractory Multiple Myeloma and Relapsed/ Refractory Plasma Cell Leukemia |
| 2027-01-03 | Ex-US | CRTHF | CARsgen Therapeutics Holdings Limited | Phase 1 | A Study of CT0596 in Plasma Cell Leukemia |
| 2027-01-04 | Ex-US | PHCUF | Photocure ASA | Phase 3 | Outcomes of High-risk Non-muscle Invasive Bladder Cancer Treated With Blue Light Resection |
| 2027-01-07 | US | IDYA | IDEAYA Biosciences, Inc. | Phase 1 | Study of IDE397 in Participants With Solid Tumors Harboring MTAP Deletion |
| 2027-01-08 | US | FTRE | Fortrea Holdings Inc. | Phase 3 | Study to Evaluate the Efficacy and Safety of Intravitreal OTX-TKI (Axitinib Implant) in Subjects With Neovascular Age- Related Macular Degeneration |
| 2027-01-08 | US | OCUL | Ocular Therapeutix, Inc. | Phase 3 | Study to Evaluate the Efficacy and Safety of Intravitreal OTX-TKI (Axitinib Implant) in Subjects With Neovascular Age- Related Macular Degeneration |
| 2027-01-13 | US | FTRE | Fortrea Holdings Inc. | Phase 3 | A Study to Investigate Changes in Symptoms in Adult Participants With Chronic Rhinosinusitis With Nasal Polyposis Initiating Treatment With Tezepelumab |
| 2027-01-15 | US | AZTR | Azitra, Inc. | Phase 2 | A Study to Evaluate Topical ATR04-484 for EGFRi-Associated Dermal Toxicity |
| 2027-01-15 | US | IDYA | IDEAYA Biosciences, Inc. | Phase 3 | IDE196 (Darovasertib) in Combination With Crizotinib as First-line Therapy in Metastatic Uveal Melanoma |
| 2027-01-15 | US | MLTX | MoonLake Immunotherapeutics | Phase 3 | Evaluation of Sonelokimab in Patients With Active Psoriatic Arthritis and Anti-TNFα Inadequate Response |
| 2027-01-15 | US | XBIT | XBiotech Inc. | Phase 2 | Natrunix in Combination With Methotrexate for Rheumatoid Arthritis Treatment |
| 2027-01-16 | US | CRBP | Corbus Pharmaceuticals Holdings, Inc. | Phase 2 | A Phase 1/2 Study to Investigate CRB-701 in Solid Tumors |
| 2027-01-25 | US | SGMT | Sagimet Biosciences Inc. | Phase 1 | Study of TVB-2640 in Men With Metastatic Castration-Resistant Prostate Cancer |
| 2027-01-29 | US | DVAX | Dynavax Technologies Corporation | Phase 2 | Immunogenicity, Safety, and Tolerability of rF1V-1018 Vaccine in Adults 18 to 55 Years of Age |
| 2027-01-29 | US | IDYA | IDEAYA Biosciences, Inc. | Phase 2 | Study of IDE196 in Patients With Solid Tumors Harboring GNAQ/11 Mutations or PRKC Fusions |
| 2027-01-31 | US | APLM | Apollomics, Inc. | Phase 2 | Safety and Efficacy of Combining APL-101 With Frontline Osimertinib in Patients With EGFR-mutated Metastatic Non-small Cell Lung Cancer (NSCLC) |
| 2027-01-31 | US | CELZ | Creative Medical Technology Holdings, Inc. | Phase 2 | Safety and Efficacy of CELZ-201 in Patients With Recent Onset Type 1 Diabetes |
| 2027-01-31 | US | CUE | Cue Biopharma, Inc. | Phase 1 | CUE-102 in Recurrent Glioblastoma |
| 2027-01-31 | Ex-US | SCNLF | Scancell Holdings plc | Phase 2 | SCIB1 and iSCIB1+ in Melanoma Patients Receiving Nivolumab With Ipilimumab or SCIB1 With Pembrolizumab (The SCOPE Study) |
| 2027-02-01 | US | ABCL | AbCellera Biologics Inc. | Phase 2 | Study Evaluating ABCL635 for Vasomotor Symptoms of Menopause |
| 2027-02-01 | US | AMLX | Amylyx Pharmaceuticals, Inc. | Phase 1 | AMX0114 in Adult Participants With Amyotrophic Lateral Sclerosis |
| 2027-02-01 | Ex-US | BVNRY | Bavarian Nordic A/S | Phase 2 | A Phase 2 Trial in Healthy Adult Participants of the Recombinant MVA-BN-WEV Vaccine |
| 2027-02-01 | US | CING | Cingulate Inc. | Phase 3 – Suspended | Phase 3 Efficacy and Safety Laboratory Classroom Study in Pediatrics (6-12) With ADHD Using CTx-1301 |
| 2027-02-01 | US | CING | Cingulate Inc. | Phase 3 – Suspended | Phase 3 Efficacy and Safety Laboratory Classroom Study in Pediatrics (6-12) With ADHD Using CTx-1301 |
| 2027-02-01 | US | DAWN | Day One Biopharmaceuticals, Inc. | Phase 2 | A Study of Emiltatug Ledadotin (Emi-Le) in Participants With Solid Tumors |
| 2027-02-01 | US | DNLI | Denali Therapeutics Inc. | Phase 1 | A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of DNL628 in Participants With Early Alzheimer's Disease |
| 2027-02-01 | US | ENLV | Enlivex Therapeutics Ltd. | Phase 2 | Intra-Articular Allocetra in Patients With Primary Knee Osteoarthritis |
| 2027-02-01 | US | FBRX | Forte Biosciences, Inc. | Phase 1 | A Study Testing the Safety and Effects of FB102 in Healthy Volunteers |
| 2027-02-01 | US | GERN | Geron Corporation | Phase 1 | A Study to Evaluate the Safety, Pharmacokinetics, Pharmacodynamics and Clinical Activity of Imetelstat in Combination With Ruxolitinib in Participants With Myelofibrosis |
| 2027-02-01 | US | GNLX | Genelux Corporation | Phase 2 | Efficacy & Safety of Olvimulogene Nanivacirepvec & Platinum-doublet + Physician's Choice of Immune Checkpoint Inhibitor Compared to Docetaxel in NSCL Cancer |
| 2027-02-01 | US | IRON | Disc Medicine, Inc. | Phase 2 | A Phase 2, Open-Label Study of DISC-3405 in Participants With Polycythemia Vera (PV) |
| 2027-02-01 | US | KOD | Kodiak Sciences Inc. | Phase 3 | A Phase 3 Study to Evaluate the Efficacy and Safety of Intravitreal KSI-101 in Participants With Macular Edema Secondary to Inflammation (MESI) – PINNACLE |
| 2027-02-01 | US | KPTI | Karyopharm Therapeutics Inc. | Phase 1 | Eltanexor and Venetoclax in Relapsed or Refractory Myelodysplastic Syndrome and Acute Myeloid Leukemia |
| 2027-02-01 | US | KYTX | Kyverna Therapeutics, Inc. | Phase 1 | CARTIMMUNE: Study of Patients With Autoimmune Diseases Receiving KYV-101 |
| 2027-02-01 | Ex-US | LBTSF | Almirall, S.A. | Phase 2 | A Proof-of-Concept Study of LAD328 in Adults With Hidradenitis Suppurativa |
| 2027-02-01 | US | SEPN | Septerna, Inc. | Phase 1 | A Study to Evaluate Single and Multiple Doses of SEP-479 in Healthy Adult Participants |
| 2027-02-01 | US | SNDX | Syndax Pharmaceuticals, Inc. | Phase 1 | A Study of SNDX-5613 in Combination With Intensive Chemotherapy in Participants With Acute Myeloid Leukemias |
| 2027-02-01 | US | SXTP | 60 Degrees Pharmaceuticals, Inc. | Phase 2 | B-FREE Chronic Babesiosis Study |
| 2027-02-01 | US | TVRD | Tvardi Therapeutics, Inc. | Phase 2 | A Study of TTI-101 as Monotherapy and in Combination in Participants With Locally Advanced or Metastatic, and Unresectable Hepatocellular Carcinoma |
| 2027-02-01 | US | XNCR | Xencor, Inc. | Phase 1 | Study of XmAb®819 in Subjects With Advanced Clear Cell Renal Cell Carcinoma |
| 2027-02-02 | US | LNTH | Lantheus Holdings, Inc. | Phase 1 | A Pilot Study to Assess the Clinical Utility of PYLARIFY PET-CT for Detecting Metastasis in Pancreatic Cancer, Hepatocellular Carcinoma and Breast Cancer |
| 2027-02-04 | US | MLTX | MoonLake Immunotherapeutics | Phase 3 | Evaluation of Sonelokimab in Patients With Active Psoriatic Arthritis Naive to Biologic Disease-Modifying Antirheumatic Drug |
| 2027-02-07 | US | SRNE | Sorrento Therapeutics, Inc. | Phase 1 | Resiniferatoxin to Treat Severe Pain Associated With Advanced Cancer |
| 2027-02-12 | US | OCGN | Ocugen, Inc. | Phase 3 | A Phase 3 Study Of OCU400 Gene Therapy for the Treatment Of Retinitis Pigmentosa |
| 2027-02-15 | Ex-US | CASBF | CanSino Biologics Inc. | Phase 3 | A Study to Evaluate the Immunogenicity and Safety of 13-valent Pneumococcal Conjugate Vaccine (PCV13i) in Healthy Infants Aged 2 Months (Minimum 6 Weeks) |
| 2027-02-17 | US | NVCR | NovoCure Limited | Phase 1 | A Phase I Study of the NovoTTF-200M and Novo TTF-200A Systems for the Treatment of Refractory Spinal Metastasis |
| 2027-02-28 | US | FBRX | Forte Biosciences, Inc. | Phase 2 | Randomized, Double Blind, Placebo-controlled Phase 2 Study in Adults With Celiac Disease |
| 2027-02-28 | US | INSP | Inspire Medical Systems, Inc. | Phase 3 | Effects of Hypoglossal Nerve Stimulation on Cognition and Language in Down Syndrome and Obstructive Sleep Apnea |
| 2027-02-28 | Ex-US | MRCHF | H.U. Group Holdings, Inc. | Phase 3 | Phase III Non-Inferiority Trial of Proton Versus Photon Therapy for Nasopharyngeal Carcinoma |
| 2027-02-28 | US | NTHI | NeOnc Technologies Holdings, Inc. | Phase 2 | Safety and Efficacy of NEO212 in Patients With Astrocytoma IDH-mutant, Glioblastoma IDH-wildtype or Brain Metastasis |
| 2027-03-01 | Ex-US | ACHFF | Arch Biopartners Inc. | Phase 2 | LSALT Peptide for Prevention or Attenuation of Acute Kidney Injury (AKI) in Patients Undergoing On-Pump Cardiac Surgery |
| 2027-03-01 | US | ACLX | Arcellx, Inc. | Phase 1 | A Phase 1 Study of Anitocabtagene Autoleucel for the Treatment of Subjects With Non-oncology Plasma Cell-related Diseases |
| 2027-03-01 | US | ADCT | ADC Therapeutics SA | Phase 2 | Loncastuximab Tesirine and Rituximab as Bridging Therapy Before Standard-of-care CAR-T Therapy in Patients With Large B-cell Lymphoma (CORAL) |
| 2027-03-01 | US | AGIO | Agios Pharmaceuticals, Inc. | Phase 2 | AG-120 in People With IDH1 Mutant Chondrosarcoma |
| 2027-03-01 | US | ALGS | Aligos Therapeutics, Inc. | Phase 2 | A Study Evaluating the Efficacy and Safety of ALG-000184 Compared With Tenofovir Disoproxil Fumarate in Untreated HBeAg-Positive and HBeAg- Negative Adult Subjects With Chronic Hepatitis B (B-SUPREME) |
| 2027-03-01 | US | ALLR | Allarity Therapeutics, Inc. | Phase 2 | Investigation of the Anti-tumor Effect of 2X-121 in Patients With Recurrent, Advanced Ovarian Cancer |
| 2027-03-01 | US | AURA | Aura Biosciences, Inc. | Phase 1 | A Phase 1, Open-label Trial of Belzupacap Sarotalocan (AU-011) in Bladder Cancer |
| 2027-03-01 | US | CGEN | Compugen Ltd. | Phase 2 | A Clinical Trial to Evaluate the Safety and Efficacy of COM701 in Relapsed Platinum Sensitive Ovarian Cancer |
| 2027-03-01 | US | CLDX | Celldex Therapeutics, Inc. | Phase 1 | A Study of CDX-622 in Participants With Mild to Moderate Asthma |
| 2027-03-01 | US | DAWN | Day One Biopharmaceuticals, Inc. | Phase 2 | Tovorafenib for Treatment of Craniopharyngioma in Children and Young Adults |
| 2027-03-01 | US | DNLI | Denali Therapeutics Inc. | Phase 2 | Safety and Pharmacodynamic Effects of BIIB122 in Participants With LRRK2-Associated Parkinson's Disease (LRRK2-PD) |
| 2027-03-01 | US | DNLI | Denali Therapeutics Inc. | Phase 2 | Safety and Pharmacodynamic Effects of BIIB122 in Participants With LRRK2-Associated Parkinson's Disease (LRRK2-PD) |
| 2027-03-01 | US | EWTX | Edgewise Therapeutics, Inc. | Phase 2 | Phase 2 Study of EDG-5506 in Children and Adolescents With Duchenne Muscular Dystrophy Previously Treated With Gene Therapy |
| 2027-03-01 | US | FDMT | 4D Molecular Therapeutics, Inc. | Phase 2 | 4D-150 in Patients With Neovascular (Wet) Age-Related Macular Degeneration |
| 2027-03-01 | Ex-US | INCPF | InnoCare Pharma Limited | Phase 2 | Study of the Efficacy and Safety of ICP-332 in Participants With Prurigo Nodularis |
| 2027-03-01 | Ex-US | IUGNF | Imugene Limited | Phase 1 | CF33-hNIS-antiPDL1 for the Treatment of Metastatic Triple Negative Breast Cancer |
| 2027-03-01 | US | MNKD | MannKind Corporation | Phase 2 | INHALE-1st: Afrezza® For Youth With Newly-Diagnosed Type 1 Diabetes |
| 2027-03-01 | US | MNKD | MannKind Corporation | Phase 2 | INHALE-1st: Afrezza® For Youth With Newly-Diagnosed Type 1 Diabetes |
| 2027-03-01 | US | NUVB | Nuvation Bio Inc. | Phase 2 | Safety and Efficacy Study of NUV-1511 in Adult Patients With Advanced Solid Tumors |
| 2027-03-01 | US | NVCT | Nuvectis Pharma, Inc. | Phase 1 | A Phase 1 Clinical Study of NXP900 in Subjects With Advanced Cancers |
| 2027-03-01 | US | OCGN | Ocugen, Inc. | Phase 2 | Study to Assess the Safety and Efficacy of OCU400 for Retinitis Pigmentosa and Leber Congenital Amaurosis |
| 2027-03-01 | US | OCUL | Ocular Therapeutix, Inc. | Phase 3 | A Study to Evaluate the Efficacy and Safety of OTX-TKI (Axitinib Implant) in Participants With Non-Proliferative Diabetic Retinopathy |
| 2027-03-01 | US | PEPG | PepGen Inc. | Phase 2 | A Clinical Study of PGN-EDODM1 in People With Myotonic Dystrophy Type 1 |
| 2027-03-01 | US | PMVP | PMV Pharmaceuticals, Inc. | Phase 1 | A Study to Investigate the Effects of Multiple Doses of Rezatapopt on the Pharmacokinetics of Metformin, Rosuvastatin, Repaglinide, and Midazolam in Patients With Advanced Solid Tumors Harboring a TP53 Y220C Mutation. |
| 2027-03-01 | US | PSTV | Plus Therapeutics, Inc. | Phase 1 | Determine Maximum Tolerated Dose, Safety, and Tolerability of Rhenium (186Re) in Pediatric Recurrent, Refractory or Progressive Ependymoma and High-Grade Glioma |
| 2027-03-01 | US | STOK | Stoke Therapeutics, Inc. | Phase 3 | A Double-blind Study Evaluating the Efficacy, Safety, and Tolerability of Zorevunersen in Patients With Dravet Syndrome |
| 2027-03-01 | US | SXTP | 60 Degrees Pharmaceuticals, Inc. | Phase 2 | Oral Tafenoquine Plus Standard of Care Versus Placebo Plus Standard of Care for Babesiosis |
| 2027-03-01 | US | THAR | Tharimmune, Inc. | Phase 2 | TH104 for the Treatment of Pruritus in Primary Biliary Cholangitis |
| 2027-03-01 | US | URGN | UroGen Pharma Ltd. | Phase 3 | A Phase 3 Single-arm Study of UGN-104 for the Treatment of Low-grade Upper Tract Urothelial Cancer |
| 2027-03-01 | US | VSTM | Verastem, Inc. | Phase 2 | A Study of Avutometinib (VS-6766) and Defactinib in People With Mesonephric Gynecologic Cancer |
| 2027-03-02 | US | SNDX | Syndax Pharmaceuticals, Inc. | Phase 1 | Revumenib in Combination With 7+3 + Midostaurin in AML |
| 2027-03-07 | Ex-US | ASPHF | Ascentage Pharma Group International | Phase 2 | Phase II Study Assessing the Efficacy and Toxicity of Olverembatinib Monotherapy in Patients With Newly Diagnosed Chronic Myeloid Leukemia in Chronic Phase |
| 2027-03-08 | Ex-US | ORYZF | Oryzon Genomics S.A. | Phase 1 | Iadademstat in Combination With Azacitidine and Venetoclax in Treating Newly Diagnosed Acute Myeloid Leukemia |
| 2027-03-10 | US | FBRX | Forte Biosciences, Inc. | Phase 1 | A Study to Evaluate the Safety and Efficacy of FB102 in Patients With Severe to Very Severe Alopecia Areata. |
| 2027-03-12 | US | TSHA | Taysha Gene Therapies, Inc. | Phase 2 | First-in-Human Study of TSHA-101 Gene Therapy for Treatment of Infantile Onset GM2 Gangliosidosis |
| 2027-03-12 | US | TVTX | Travere Therapeutics, Inc. | Phase 2 | Study of Sparsentan Treatment in Pediatrics With Proteinuric Glomerular Diseases |
| 2027-03-12 | US | TVTX | Travere Therapeutics, Inc. | Phase 2 | Study of Sparsentan Treatment in Pediatrics With Proteinuric Glomerular Diseases |
| 2027-03-14 | US | ZLAB | Zai Lab Limited | Phase 3 | A Study to Assess the Efficacy and Safety of ZL-1109 in Chinese Participants With Active Thyroid Eye Disease |
| 2027-03-15 | US | CLDX | Celldex Therapeutics, Inc. | Phase 2 | Pembrolizumab Combined With Bevacizumab With or Without Agonist Anti-CD40 CDX-1140 for the Treatment of Patients With Recurrent Ovarian Cancer |
| 2027-03-31 | US | ALT | Altimmune, Inc. | Phase 2 | RESTORE TRIAL: A Phase 2 Study Evaluating the Efficacy and Safety of Pemvidutide in the Treatment of Alcohol-Associated Liver Disease (ALD) |
| 2027-03-31 | Ex-US | ASPHF | Ascentage Pharma Group International | Phase 3 | A Study of Olverembatinib in SDH-deficient GIST. |
| 2027-03-31 | US | CGON | CG Oncology, Inc. | Phase 2 | Phase 2 Study to Evaluate Safety and Efficacy of Cretostimogene Grenadenorepvec in High-Risk NMIBC |
| 2027-03-31 | US | CLDX | Celldex Therapeutics, Inc. | Phase 2 | DC Migration Study to Evaluate TReg Depletion In GBM Patients With and Without Varlilumab |
| 2027-03-31 | US | HURA | TuHURA Biosciences, Inc. | Phase 3 | Placebo-Controlled Trial of IFx-Hu2.0 Followed By Pembrolizumab In Checkpoint Inhibitor Naïve Participants With Advanced Or Metastatic Merkel Cell Carcinoma |
| 2027-03-31 | Ex-US | KSPHF | Kissei Pharmaceutical Co., Ltd. | Phase 3 | Confirmatory Study 3 of KPS-0373 in Patients With Spinocerebellar Degeneration |
| 2027-03-31 | US | LEGN | Legend Biotech Corporation | Phase 1 | A Clinical Study to Evaluate LVIVO-TaVec200 for the Treatment of Relapsed/Refractory Multiple Myeloma |
| 2027-03-31 | Ex-US | MSCLF | Satellos Bioscience Inc. | Phase 2 | Phase 2 Study of SAT-3247 in Pediatric Ambulatory Patients |
| 2027-03-31 | US | TNGX | Tango Therapeutics, Inc. | Phase 2 | Safety and Tolerability of TNG456 Alone and in Combination With Abemaciclib in Patients With Solid Tumors With MTAP Loss |
| 2027-04-01 | US | ABCL | AbCellera Biologics Inc. | Phase 1 | A First-in-Human Phase 1 Single-Ascending Dose Study of ABCL575 in Healthy Participants |
| 2027-04-01 | US | ASRT | Assertio Holdings, Inc. | Phase 2 | Intra-nasal Ketorolac for Acute Ureteral Stent-associated Pain Following Ureteroscopy for Stone Disease |
| 2027-04-01 | US | CGTX | Cognition Therapeutics, Inc. | Phase 2 | A Study to Evaluate the Safety and Efficacy of CT1812 in Early Alzheimer's Disease |
| 2027-04-01 | Ex-US | CHIZF | China Traditional Chinese Medicine Holdings Co. Limited | Phase 3 | Xian-Lian-Jie-Du Optimization Decoction As an Adjuvant Treatment for Prevention of Recurrence of Colon Cancer |
| 2027-04-01 | US | CLYM | Climb Bio Inc | Phase 1 | A Phase 1b Study of Budoprutug in Systemic Lupus Erythematosus (SLE) |
| 2027-04-01 | US | HRMY | Harmony Biosciences Holdings, Inc. | Phase 3 | A Study of EPX-100 (Clemizole Hydrochloride) in Participants With Dravet Syndrome |
| 2027-04-01 | US | KOD | Kodiak Sciences Inc. | Phase 3 | A Phase 3 Study to Evaluate the Efficacy and Safety of Intravitreal KSI-101 in Participants With Macular Edema Secondary to Inflammation (MESI) – PEAK |
| 2027-04-01 | US | KPTI | Karyopharm Therapeutics Inc. | Phase 2 | Selinexor and Backbone Treatments of Multiple Myeloma Patients |
| 2027-04-01 | US | KYTX | Kyverna Therapeutics, Inc. | Phase 2 | KYSA-7: A Study of Anti-CD19 CAR T-Cell Therapy, in Subjects With Refractory Primary and Secondary Progressive Multiple Sclerosis |
| 2027-04-01 | US | MIRM | Mirum Pharmaceuticals, Inc. | Phase 2 | A Study to Evaluate Efficacy and Safety of an Investigational Drug Named Volixibat in Patients With Itching Caused by Primary Biliary Cholangitis |
| 2027-04-01 | US | NKTX | Nkarta, Inc. | Phase 2 | A Phase 1/2 Study of NKX019 in Subjects With Autoimmune Disease (Ntrust-1) |
| 2027-04-01 | US | RAPT | RAPT Therapeutics, Inc. | Phase 2 | Phase 2b Study of RPT904 as Monotherapy in Participants With IgE-Mediated Food Allergy |
| 2027-04-01 | US | RCUS | Arcus Biosciences, Inc. | Phase 2 | Combination Therapy in Patients With Localized Pancreatic Ductal Adenocarcinoma |
| 2027-04-01 | US | TLSA | Tiziana Life Sciences Ltd | Phase 2 | A Phase 2a Study of Foralumab Nasal in Patients With Multiple System Atrophy (MSA) |
| 2027-04-01 | US | VSTM | Verastem, Inc. | Phase 2 | A Study of Avutometinib, Defactinib, and Letrozole in People With Low-Grade Serous Ovarian Cancer |
| 2027-04-01 | US | XENE | Xenon Pharmaceuticals Inc. | Phase 3 | A Study to Evaluate XEN1101 as Adjunctive Therapy in Primary Generalized Tonic-Clonic Seizures |
| 2027-04-15 | US | CLDX | Celldex Therapeutics, Inc. | Phase 1 | Personalized TCR-T: Study of Adoptively Transferred T-cell Receptor Gene-engineered T Cells (TCR-T) |
| 2027-04-24 | US | ZJYL | Jin Medical International Ltd. | Phase 2 | Assess the Efficacy of Radiotherapy and Sequential Chemotherapy and AK104 Before TME Surgery for Local CRC(AK104-IIT-13) |
| 2027-04-25 | Ex-US | ALMRY | Almirall SA | Phase 3 | A Study of Lebrikizumab Treatment in Adults and Adolescents With Moderate-to-Severe Atopic Dermatitis |
| 2027-04-25 | Ex-US | LBTSF | Almirall, S.A. | Phase 3 | A Study of Lebrikizumab Treatment in Adults and Adolescents With Moderate-to-Severe Atopic Dermatitis |
| 2027-04-25 | US | PYXS | Pyxis Oncology, Inc. | Phase 1 | A Study of PYX-201 in Advanced Solid Tumors |
| 2027-04-26 | US | TLX | Telix Pharmaceuticals Limited | Phase 1 | Samarium Optimized for Long-lasting Analgesia in Cancerous End-stage Bone Pain |
| 2027-04-30 | US | IDYA | IDEAYA Biosciences, Inc. | Phase 2 | (Neo)Adjuvant IDE196 (Darovasertib) in Patients With Localized Ocular Melanoma |
| 2027-04-30 | US | IOVA | Iovance Biotherapeutics, Inc. | Phase 2 | LN-145 or LN-145-S1 in Treating Patients With Relapsed or Refractory Ovarian Cancer, Triple Negative Breast Cancer (TNBC), Anaplastic Thyroid Cancer, Osteosarcoma, or Other Bone and Soft Tissue Sarcomas |
| 2027-04-30 | US | NBTX | Nanobiotix S.A. | Phase 1 | NBTXR3 Activated by Radiotherapy for Patients With Advanced Cancers Treated With An Anti-PD-1 Therapy |
| 2027-04-30 | Ex-US | NPPNY | Nippon Shinyaku Co., Ltd. | Phase 2 | Extension Study of NS-089/NCNP-02 in DMD |
| 2027-04-30 | US | RCUS | Arcus Biosciences, Inc. | Phase 2 | Neoadjuvant Atezolizumab-Based Combination Therapy in Men With Localized Prostate Cancer Prior to Radical Prostatectomy |
| 2027-04-30 | US | RLAY | Relay Therapeutics, Inc. | Phase 1 | First-in-Human Study of Mutant-selective PI3Kα Inhibitor, RLY-2608, as a Single Agent in Patients With Advanced Solid Tumors and in Combination With Endocrine Therapy +/- a CDK4/6 or CDK4 Inhibitor in Patients With Advanced Solid Tumors or Advanced Breast Cancer |
| 2027-05-01 | US | ADPT | Adaptive Biotechnologies Corporation | Phase 2 | Assessing Minimal Residual Disease by Next- Generation Sequencing to Minimize Exposure in People With CLL or SLL Who Have Been Treated With Venetoclax |
| 2027-05-01 | US | AGIO | Agios Pharmaceuticals, Inc. | Phase 2 – Withdrawn | A Study of Mitapivat in Participants With Sickle Cell Disease and Nephropathy |
| 2027-05-01 | US | BOLT | Bolt Biotherapeutics, Inc. | Phase 2 | A First-in-Human Study Using BDC-4182 as a Single Agent in Advanced Gastric and Gastroesophageal Cancer |
| 2027-05-01 | US | CMPX | Compass Therapeutics, Inc. | Phase 2 | CTX-009 With Gemcitabine, Cisplatin, and Durvalumab as First-line Therapy in Patients With Unresectable or Metastatic Biliary Tract Cancers |
| 2027-05-01 | US | IOVA | Iovance Biotherapeutics, Inc. | Phase 1 | A Study of LN-144 or LN-145 in People With Advanced Uveal Melanoma, Undifferentiated Pleomorphic Sarcoma, or Dedifferentiated Liposarcoma |
| 2027-05-01 | US | JBIO | Jade Biosciences, Inc. | Phase 1 | A Single Dose, Phase 1 Study of JADE101 in Healthy Japanese and Chinese Participants |
| 2027-05-01 | US | MGNX | MacroGenics, Inc. | Phase 2 – Suspended | Regorafenib (Reg) and Lorigerlimab (Lor), RELO Regimen, in Treatment of High-risk Patients With Colorectal Cancer With Radiographic Occult Molecular Residual Disease After End of Established Definitive Therapy [ReLOAD Trial] |
| 2027-05-01 | US | RCUS | Arcus Biosciences, Inc. | Phase 1 | A Study to Evaluate the Safety and Tolerability of AB680 in Participants With Gastrointestinal Malignancies |
| 2027-05-01 | US | RCUS | Arcus Biosciences, Inc. | Phase 2 | Study Evaluating Effectiveness and Safety of Zimberelimab and Domvanalimab in Lung Cancer |
| 2027-05-01 | US | VSTM | Verastem, Inc. | Phase 2 – Suspended | A Study of VS-6766 and Cetuximab in Patients With Advanced Colorectal Cancer |
| 2027-05-01 | US | VXRT | Vaxart, Inc. | Phase 2 | A Study to Evaluate VXA-CoV2-3.3 COVID-19 Vaccine Against Currently Approved/Authorized mRNA COVID-19 Injectable Booster Vaccine in Adults Previously Immunized Against COVID-19 Infection |
| 2027-05-01 | US | VYGR | Voyager Therapeutics, Inc. | Phase 2 | VY7523-102: Randomized, Placebo-Controlled, Double-Blind, Multiple Ascending Dose Study in Participants With Early Alzheimer's Disease |
| 2027-05-01 | US | XENE | Xenon Pharmaceuticals Inc. | Phase 3 | A Randomized Study of Azetukalner Versus Placebo in Major Depressive Disorder (X-NOVA3) |
| 2027-05-01 | US | ZURA | Zura Bio Limited | Phase 2 | Tibulizumab Systemic Sclerosis Understanding and Response Evaluation (TibuSURE) |
| 2027-05-05 | US | FTRE | Fortrea Holdings Inc. | Phase 1 | A Study to Investigate Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of AZD5492 in Adult Participants With Systemic Lupus Erythematosus or Idiopathic Inflammatory Myopathies or Rheumatoid Arthritis. |
| 2027-05-06 | US | SLDB | Solid Biosciences Inc. | Phase 2 | A Study of SGT-003 Gene Therapy in Duchenne Muscular Dystrophy (INSPIRE DUCHENNE) |
| 2027-05-25 | Ex-US | ALMRY | Almirall SA | Phase 2 | A Study of LAD191 in Adults With Hidradenitis Suppurativa |
| 2027-05-25 | Ex-US | LBTSF | Almirall, S.A. | Phase 2 | A Study of LAD191 in Adults With Hidradenitis Suppurativa |
| 2027-05-26 | US | FDMT | 4D Molecular Therapeutics, Inc. | Phase 1 | Dose Escalation Study of Intravitreal 4D-110 in Patients With Choroideremia |
| 2027-05-27 | US | MBX | MBX Biosciences, Inc. | Phase 2 | Extension Study to Evaluate the Long-Term Safety and Tolerability of MBX 2109 in Patients With Hypoparathyroidism |
| 2027-05-30 | US | ACRV | Acrivon Therapeutics, Inc. | Phase 2 | A Phase 2 Study of ACR-368 in Endometrial Adenocarcinoma |
| 2027-05-30 | US | OLMA | Olema Pharmaceuticals, Inc. | Phase 1 | Phase 1 Study of OP-3136 in Advanced or Metastatic Solid Tumors |
| 2027-05-30 | US | ZLAB | Zai Lab Limited | Phase 1 | A Study of ZL-1310 in Subjects With Small Cell Lung Cancer |
| 2027-05-31 | US | DAWN | Day One Biopharmaceuticals, Inc. | Phase 2 | A Study to Evaluate Tovorafenib in Pediatric and Young Adult Participants With Relapsed or Progressive Low-Grade Glioma and Advance Solid Tumors |
| 2027-05-31 | Ex-US | LBTSF | Almirall, S.A. | Phase 1 | A Study of LAD106 in Healthy Adult Participants |
| 2027-05-31 | US | RIGL | Rigel Pharmaceuticals, Inc. | Phase 2 | Fostamatinib for Treating Acute Respiratory Distress Syndrome (ARDS) in Hospitalized Adults |
| 2027-05-31 | US | SRPT | Sarepta Therapeutics, Inc. | Phase 3 | A Gene Transfer Therapy Study to Evaluate the Safety and Efficacy of Delandistrogene Moxeparvovec (SRP-9001) in Non-Ambulatory and Ambulatory Participants With Duchenne Muscular Dystrophy (DMD) |
| 2027-06-01 | US | AKBA | Akebia Therapeutics, Inc. | Phase 2 | A Study of Praliciguat in Participants With Focal Segmental Glomerulosclerosis (FSGS) |
| 2027-06-01 | US | ALXO | ALX Oncology Holdings Inc. | Phase 1 | A First in Human Study of ALX2004 With Advanced or Metastatic Selected Solid Tumors |
| 2027-06-01 | US | APRE | Aprea Therapeutics, Inc. | Phase 1 | Study of APR-1051 in Patients With Advanced Solid Tumors |
| 2027-06-01 | US | BLLN | BillionToOne, Inc. | Phase 1 | Response Adapted Neoadjuvant Therapy in Gastroesophageal Cancers (RANT-GC Trial) |
| 2027-06-01 | US | BMEA | Biomea Fusion, Inc. | Phase 2 | Phase 2 Trial of Icovamenib in Participants With Type 2 Diabetes Who Are Not Achieving Glycemic Targets |
| 2027-06-01 | US | BMEA | Biomea Fusion, Inc. | Phase 2 | Phase 2 Trial of Icovamenib in Participants With Type 2 Diabetes Mellitus Who Are Not Achieving Glycemic Targets While Using GLP-1-Based Therapy |
| 2027-06-01 | Ex-US | CHIZF | China Traditional Chinese Medicine Holdings Co. Limited | Phase 3 | EFG vs IVIG in TAMG |
| 2027-06-01 | US | CRVS | Corvus Pharmaceuticals, Inc. | Phase 2 | Study to Evaluate Soquelitinib in Participants With Moderate to Severe AD |
| 2027-06-01 | US | DAWN | Day One Biopharmaceuticals, Inc. | Phase 3 | DAY101 vs. Standard of Care Chemotherapy in Pediatric Participants With Low-Grade Glioma Requiring First-Line Systemic Therapy (LOGGIC/FIREFLY-2) |
| 2027-06-01 | US | DNLI | Denali Therapeutics Inc. | Phase 3 | An Extension Study of the Long-Term Safety, Tolerability, and Efficacy of Tividenofusp Alfa (DNL310) in Participants With Mucopolysaccharidosis Type II (MPS II) From Study DNLI-E-0002 or Study DNLI-E-0007 |
| 2027-06-01 | US | FDMT | 4D Molecular Therapeutics, Inc. | Phase 2 | 4D-710 in Adult Patients With Cystic Fibrosis |
| 2027-06-01 | US | FDMT | 4D Molecular Therapeutics, Inc. | Phase 3 | 4D-150 in Patients With Macular Neovascularization Secondary to Age-Related Macular Degeneration |
| 2027-06-01 | US | HUMA | Humacyte, Inc. | Phase 3 | To Compare the Efficacy and Safety of the ATEV With AVF in Female Patients With End-Stage Renal Disease Requiring Hemodialysis |
| 2027-06-01 | Ex-US | IDRSF | Idorsia Ltd | Phase 2 | A Study to Learn How Safe ACT-777991 is and How Well it Works in Adults With Non-segmental Vitiligo |
| 2027-06-01 | US | IMMP | Immutep Limited | Phase 3 | Study of Eftilagimod Alfa (Efti) in Combination With Pembrolizumab and Chemotherapy Versus Placebo in Combination With Pembrolizumab and Chemotherapy in Participants With Metastatic Non-Small Cell Lung Cancer (NSCLC) (TACTI-004) |
| 2027-06-01 | US | INBX | Inhibrx Biosciences, Inc. | Phase 2 | Neoadjuvant INBRX-106 in Combination With Pembrolizumab for Stage II/III TNBC Patients |
| 2027-06-01 | Ex-US | INCPF | InnoCare Pharma Limited | Phase 1 | ICP-248 in Combination With Azacitidine for the Treatment in Patients With Myeloid Malignancies |
| 2027-06-01 | US | IRON | Disc Medicine, Inc. | Phase 1 | A Phase 1b, Open-Label Study of DISC-3405 in Participants With Sickle Cell Disease (SCD) |
| 2027-06-01 | Ex-US | IUGNF | Imugene Limited | Phase 1 | Dose-escalation and Dose-expansion Study of Safety of Azer-cel (PBCAR0191) in Participants With Relapsed/Refractory (r/r) Non-Hodgkin Lymphoma (NHL) and r/r B-cell Acute Lymphoblastic Leukemia (B-ALL) |
| 2027-06-01 | Ex-US | KHTRF | Knight Therapeutics Inc. | Phase 2 | Dose Escalation For INtraprostatic LEsions |
| 2027-06-01 | US | KPTI | Karyopharm Therapeutics Inc. | Phase 2 | A Study of Selinexor Monotherapy in Subjects With JAK Inhibitor-naïve Myelofibrosis and Moderate Thrombocytopenia |
| 2027-06-01 | US | KYTX | Kyverna Therapeutics, Inc. | Phase 1 | A Study of Anti-CD19 Chimeric Antigen Receptor T-Cell ( CAR-T) Therapy in Subjects With Non-relapsing and Progressive Forms of Multiple Sclerosis |
| 2027-06-01 | US | KYTX | Kyverna Therapeutics, Inc. | Phase 2 | Comparison of B-cell Depletion by Rituximab and Anti-CD 19 CAR-T Therapy in Patients With Rheumatoid Arthritis |
| 2027-06-01 | US | LBRX | LB Pharmaceuticals Inc. | Phase 3 | Study to Evaluate LB-102 for the Treatment of Adult Patients With Acute Schizophrenia (NOVA-2) |
| 2027-06-01 | US | MIST | Milestone Pharmaceuticals Inc. | Phase 2 | The NODE-202 Study (Study of Etripamil Nasal Spray in Pediatric Patients) |
| 2027-06-01 | US | NMRA | Neumora Therapeutics, Inc. | Phase 3 | Study to Assess the Safety and Effectiveness of NMRA-335140-501 |
| 2027-06-01 | US | ORKA | Oruka Therapeutics, Inc. | Phase 2 | Dose Ranging Study of ORKA-001 in Patients With Moderate-to-Severe Plaque Psoriasis |
| 2027-06-01 | US | PHVS | Pharvaris N.V. | Phase 3 | Extension Study of Oral PHA-022121 for Acute Treatment of Angioedema Attacks in Patients With Hereditary Angioedema |
| 2027-06-01 | US | PHVS | Pharvaris N.V. | Phase 3 | Study of Oral Deucrictibant XR Tablet for Prophylaxis and Deucrictibant IR Capsule for On-Demand Treatment of Angioedema Attacks in Adults With Acquired Angioedema Due to C1 Inhibitor Deficiency |
| 2027-06-01 | US | RIGL | Rigel Pharmaceuticals, Inc. | Phase 2 | Olutasidenib Combined With Co-targeted Therapy in Relapsed or Refractory IDH1-mutated Myeloid Malignancies Harboring Activated Signaling Pathway Mutations |
| 2027-06-01 | US | RXRX | Recursion Pharmaceuticals, Inc. | Phase 2 | Evaluate REC-4881 in Participants With Familial Adenomatous Polyposis (FAP) |
| 2027-06-01 | US | SLDB | Solid Biosciences Inc. | Phase 1 | A Study of SGT-501 Gene Therapy in Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) |
| 2027-06-01 | US | SNSE | Sensei Biotherapeutics, Inc. | Phase 2 | A Study of SNS-101 (Anti VISTA) Monotherapy and in Combination With Cemiplimab in Patients With Advanced Solid Tumors |
| 2027-06-01 | Ex-US | SOLTF | Nxera Pharma Co., Ltd. | Phase 2 | HTL0039732 in Participants With Advanced Solid Tumours |
| 2027-06-01 | US | SRNE | Sorrento Therapeutics, Inc. | Phase 2 – Suspended | Study to Assess Epidural Resiniferatoxin for the Treatment of Intractable Pain Associated With Advanced Cancer |
| 2027-06-01 | US | SVRA | Savara Inc. | Phase 3 | Inhaled Molgramostim in Pediatric Participants With Autoimmune Pulmonary Alveolar Proteinosis (aPAP). |
| 2027-06-01 | US | TARA | Protara Therapeutics, Inc. | Phase 3 | Study of Choline Chloride for Injection in Adolescent and Adult Patients With Intestinal Failure Receiving Long Term Parenteral Support |
| 2027-06-01 | US | TLSI | TriSalus Life Sciences, Inc. | Phase 1 | Cryoablation and Arterial Infusion of SD-101 in Combination With Durvalumab and Tremelimumab |
| 2027-06-01 | US | TNGX | Tango Therapeutics, Inc. | Phase 2 | Study to Evaluate the Safety, Tolerability & Efficacy of TNG462 in Combination in PDAC & NSCLC Patients |
| 2027-06-01 | US | VRCA | Verrica Pharmaceuticals Inc. | Phase 3 | Cantharidin Application in Patients With Common Warts (Verruca Vulgaris) (COVE-2) |
| 2027-06-01 | US | VSTM | Verastem, Inc. | Phase 2 | A Phase 2 Study of VS-7375 in Patients With KRAS G12D-Mutated Colorectal Cancer |
| 2027-06-01 | US | VSTM | Verastem, Inc. | Phase 2 | A Phase 2 Study of VS-7375 in Patients With KRAS G12D-Mutated Pancreatic Cancer |
| 2027-06-01 | US | VSTM | Verastem, Inc. | Phase 2 | A Phase 2 Study of VS-7375 in Patients With KRAS G12D-Mutated Non-Small Cell Lung Cancer |
| 2027-06-01 | US | ZYME | Zymeworks Inc. | Phase 3 | Personalized Medicine for Advanced Biliary Cancer Patients |
| 2027-06-03 | Ex-US | CRTHF | CARsgen Therapeutics Holdings Limited | Phase 1 | Study of CT071 Injection in High Risk Newly Diagnosed Multiple Myeloma |
| 2027-06-09 | US | IOBT | IO Biotech, Inc. | Phase 2 | A Study of IO102/IO103, Nivolumab, and Relatlimab in People With Melanoma |
| 2027-06-15 | Ex-US | CRTHF | CARsgen Therapeutics Holdings Limited | Phase 2 | Anti-GPRC5D CAR-T Cells (CT071) in Participants With RRMM or RRpPCL |
| 2027-06-23 | Ex-US | ALMRY | Almirall SA | Phase 2 | A Study of LAD603 in Adults With Alopecia Areata |
| 2027-06-23 | Ex-US | LBTSF | Almirall, S.A. | Phase 2 | A Study of LAD603 in Adults With Alopecia Areata |
| 2027-06-25 | US | APLS | Apellis Pharmaceuticals, Inc. | Phase 2 | A Phase 2, Randomized, Placebo Controlled, Multicenter, Masked Study to Evaluate the Efficacy, Safety, Tolerability, and Pharmacodynamics of Multidose APL 3007 in Combination With Syfovre/Pegcetacoplan (APL-2) in Patients Diagnosed With Geographic Atrophy Secondary to Age Related Macular Degeneratio |
| 2027-06-25 | US | FTRE | Fortrea Holdings Inc. | Phase 3 | Open-label Study to Assess Reduction of Background Asthma Medication While Sustaining Asthma Control and Clinical Remission With Tezepelumab in Patients 12-80yrs With Severe Asthma. |
| 2027-06-25 | Ex-US | INCPF | InnoCare Pharma Limited | Phase 1 | Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of ICP-248 as Monotherapy or in Combination With Anti-CD20 Monoclonal Antibody in Mature B-cell Malignancies |
| 2027-06-30 | US | ACRS | Aclaris Therapeutics, Inc. | Phase 1 | MK2 Inhibitor in Combination With mFOLFIRINOX for Untreated Metastatic Pancreatic Ductal Adenocarcinoma |
| 2027-06-30 | Ex-US | CRTHF | CARsgen Therapeutics Holdings Limited | Phase 1 | A Clinical Study Exploring the Safety, Efficacy and Cell Metabolic Dynamics of Universal CD19 / 20 Car-t Cell Injection in Moderate to Severe Refractory Systemic Lupus Erythematosus |
| 2027-06-30 | Ex-US | CSPHF | CStone Pharmaceuticals | Phase 1 | A Study of CS5001 in Patients With Advanced Solid Tumors and Lymphomas |
| 2027-06-30 | US | IMNN | Imunon, Inc. | Phase 2 | Phase II IMNN-001 (Also Known as GEN-1) on SLL With BEV and NACT, Newly Diagnosed Advanced Ovarian, Fallopian Tube or Primary Peritoneal Cancer |
| 2027-06-30 | US | INDP | Indaptus Therapeutics, Inc. | Phase 2 | Study of DECOY20 With or Without Tislelizumab in Patients With Advanced Solid Tumors |
| 2027-06-30 | US | LEGN | Legend Biotech Corporation | Phase 1 | The CD19/CD20 Dual-Target in Vivo CAR-T Lentiviral Product in the Treatment of Relapsed/Refractory B-cell Malignancies |
| 2027-06-30 | US | MIRM | Mirum Pharmaceuticals, Inc. | Phase 3 | A Trial Evaluating Brelovitug (BJT-778) vs Bulevirtide for the Treatment of Chronic Hepatitis Delta Infection (AZURE-2) |
| 2027-06-30 | US | PBYI | Puma Biotechnology, Inc. | Phase 2 | A Study of Alisertib in Combination With Endocrine Therapy in Patients With HR-positive, HER2-negative Recurrent or Metastatic Breast Cancer |
| 2027-06-30 | US | RIGL | Rigel Pharmaceuticals, Inc. | Phase 2 | Phase 1b/2 Study of Decitabine and Venetoclax in Combination With the Targeted Mutant IDH1 Inhibitor Olutasidenib |
| 2027-06-30 | US | RLMD | Relmada Therapeutics, Inc. | Phase 3 – Withdrawn | A Study of NDV-01 as an Intravesical Administration to Patients With BCG-Unresponsive Non-Muscle Invasive Bladder Cancer (NMIBC), Refractory to First-line Therapy |
| 2027-07-01 | US | ANL | Adlai Nortye Ltd. | Phase 1 | An Initial Evaluation of AN8025 in Solid Tumors |
| 2027-07-01 | US | APLS | Apellis Pharmaceuticals, Inc. | Phase 3 | An Open-Label, Nonrandomized, Multicenter Extension Study to Evaluate the Long-term Safety and Efficacy of Pegcetacoplan in Participants With C3 Glomerulopathy or Immune-Complex Membranoproliferative Glomerulonephritis |
| 2027-07-01 | US | ARTV | Artiva Biotherapeutics, Inc. | Phase 1 | Open-label Single-Center Study to Evaluate the Safety and Efficacy of Combining Rituximab and AB-101 in B-cell Associated Autoimmune Diseases. |
| 2027-07-01 | US | BHVN | Biohaven Ltd. | Phase 1 | Study of BHV-1400 in IgA Nephropathy |
| 2027-07-01 | US | FOLD | Amicus Therapeutics, Inc. | Phase 3 | A Study to Evaluate the Safety, Efficacy, PK, PD and Immunogenicity of Cipaglucosidase Alfa/Miglustat in IOPD Subjects Aged 0 to <18 |
| 2027-07-01 | US | JANX | Janux Therapeutics, Inc. | Phase 1 | Study of JANX007 in Subjects With Metastatic Castration-Resistant Prostate Cancer (ENGAGER-PSMA-01) |
| 2027-07-01 | US | MESO | Mesoblast Limited | Phase 3 | Efficacy and Safety of Rexlemestrocel-L Combined With HA* in Participants With Moderate to Severe Chronic Low Back Pain |
| 2027-07-01 | US | MGNX | MacroGenics, Inc. | Phase 2 | A Study of Lorigerlimab in Participants With Advanced Solid Tumors |
| 2027-07-01 | US | NTLA | Intellia Therapeutics, Inc. | Phase 3 | A Phase 3 Study of NTLA-2001 in ATTRv-PN |
| 2027-07-01 | Ex-US | PBIGF | Paradigm Biopharmaceuticals Limited | Phase 3 | A Study to Investigate the Treatment Effect of Subcutaneous Injections of Pentosan Polysulfate Sodium Compared With Placebo in Adult Participants With Knee Osteoarthritis Pain. |
| 2027-07-01 | US | RCUS | Arcus Biosciences, Inc. | Phase 2 | Domvanalimab and Zimberelimab in Advanced Liver Cancers |
| 2027-07-01 | US | SGMO | Sangamo Therapeutics, Inc. | Phase 2 | Safety and Tolerability Study of ST-503 for Refractory Pain Due to Peripheral Neuropathy (Small Fiber Predominant, SFN) |
| 2027-07-01 | US | TLX | Telix Pharmaceuticals Limited | Phase 3 | Study of TLX101-Tx Plus Standard of Care (SoC) Versus SoC Alone for the Treatment of Patients With Recurrent Glioblastoma |
| 2027-07-01 | US | VKTX | Viking Therapeutics, Inc. | Phase 3 | VK2735 for Weight Management Type 2 Diabetes Phase 3 (VANQUISH 2) |
| 2027-07-01 | US | VKTX | Viking Therapeutics, Inc. | Phase 3 | VK2735 for Weight Management Phase 3 |
| 2027-07-01 | US | ZVRA | Zevra Therapeutics, Inc. | Phase 1 | An Individual Patient, Open Label Study to Use ACER-001 to Treat Combined D,L-2 Hydroxyglutaric Aciduria (C-2HGA) |
| 2027-07-30 | US | ADAG | Adagene Inc. | Phase 2 | A Study Evaluating the Efficacy and Safety of Multiple Immunotherapy-Based Treatment Combinations in Patients With Advanced Liver Cancers (Morpheus-Liver) |
| 2027-07-30 | US | ONCY | Oncolytics Biotech Inc. | Phase 2 | A Study in Advanced or Metastatic Gastrointestinal Cancers Exploring Treatment Combinations With Pelareorep and Atezolizumab |
| 2027-07-30 | US | TPST | Tempest Therapeutics, Inc. | Phase 2 | A Study Evaluating the Efficacy and Safety of Multiple Immunotherapy-Based Treatment Combinations in Patients With Advanced Liver Cancers (Morpheus-Liver) |
| 2027-07-31 | US | BTAI | BioXcel Therapeutics, Inc. | Phase 1 | Determining Efficacy and Safety of BXCL501 in Agitation Associated With Pediatric Schizophrenia and Bipolar Disorder |
| 2027-07-31 | US | KYNB | Kyntra Bio, Inc. | Phase 2 | FOR46 in Combination With Enzalutamide in Patients With Metastatic Castration Resistant Prostate Cancer |
| 2027-07-31 | US | MAIA | MAIA Biotechnology, Inc. | Phase 3 | A Phase III Study With THIO + Cemiplimab vs Chemotherapy as 3rd Line Treatment in Advanced/Metastatic NSCLC |
| 2027-07-31 | US | TGTX | TG Therapeutics, Inc. | Phase 2 | A Study to Evaluate Pharmacokinetics (PK) and Safety of Subcutaneous (SC) Ublituximab Administered at Various Injection Sites and Relative Bioavailability Via Autoinjector (AI) Versus Syringe Subcutaneously in Participants With Multiple Sclerosis (MS) |
| 2027-08-01 | US | ACAD | ACADIA Pharmaceuticals Inc. | Phase 2 | ACP-211 Monotherapy for Major Depressive Disorder With Inadequate Antidepressant Response |
| 2027-08-01 | US | ADCT | ADC Therapeutics SA | Phase 2 | Loncastuximab Tesirine in Combination With Rituximab in Patients With Relapsed or Refractory Follicular Lymphoma |
| 2027-08-01 | US | ARTV | Artiva Biotherapeutics, Inc. | Phase 1 | AB-101 in Combination With B-Cell Depleting mAb in Patients Who Failed Treatment for Class III or IV Lupus Nephritis or Other Forms of Refractory Systemic Lupus Erythematosus |
| 2027-08-01 | Ex-US | ASPHF | Ascentage Pharma Group International | Phase 3 | A Global Study of Lisaftoclax (APG-2575) Combined With Acalabrutinib Versus Immunochemotherapy for Newly Diagnosed CLL/SLL. |
| 2027-08-01 | US | BBOT | BridgeBio Oncology Therapeutics, Inc. | Phase 1 | BBO-11818 in Adult Subjects With KRAS Mutant Cancer |
| 2027-08-01 | US | BHVN | Biohaven Ltd. | Phase 3 | A Study to Determine if BHV-8000 is Effective, Safe and Tolerable as a Treatment for Adults Living With Early Parkinson's Disease |
| 2027-08-01 | US | CLLS | Cellectis S.A. | Phase 2 | Study Evaluating UCART20x22 in B-Cell Non-Hodgkin Lymphoma |
| 2027-08-01 | US | CLYM | Climb Bio Inc | Phase 2 | A Phase 1b/2a Study of Budoprutug in Subjects With Immune Thrombocytopenia (ITP) |
| 2027-08-01 | US | KPRX | Kiora Pharmaceuticals, Inc. | Phase 2 | A Phase II Study of Intravitreal KIO-301 in Patients With Late-stage Retinitis Pigmentosa |
| 2027-08-01 | US | NVCR | NovoCure Limited | Phase 1 | A Study of Tumor-Treating Fields (TTFields) in People With Lung Adenocarcinoma |
| 2027-08-01 | US | RARE | Ultragenyx Pharmaceutical Inc. | Phase 3 | Follow-up Study of AAV-Mediated Gene Transfer (UX111; Previously Known as ABO-102) for MPS Type IIIA |
| 2027-08-01 | US | RARE | Ultragenyx Pharmaceutical Inc. | Phase 3 | A Study to Determine the Effect of Triheptanoin Compared With Even-Chain MCT on MCEs in Pediatric Patients With LC-FAOD |
| 2027-08-01 | US | SUPN | Supernus Pharmaceuticals, Inc. | Phase 2 | RENAISSANCE 2: SPN-817 Phase 2, Double-Blind, Placebo-Controlled Study in Adults With Focal Onset Seizures |
| 2027-08-01 | US | TLX | Telix Pharmaceuticals Limited | Phase 2 | CAIX PET/CT for Residual or Recurrent Post-ablative ccRCC |
| 2027-08-01 | US | TNYA | Tenaya Therapeutics, Inc. | Phase 2 | Multi-center, Open-label, Single-ascending Dose Study of Safety and Tolerability of TN-201 in Adults With Symptomatic MYBPC3 Mutation-associated HCM |
| 2027-08-01 | US | TVTX | Travere Therapeutics, Inc. | Phase 3 | A Study to Investigate Efficacy and Safety of Pegtibatinase Compared With Placebo in Participants ≥12 to ≤65 Years of Age With Classical Homocystinuria (HCU) Due to Cystathionine Beta Synthase Deficiency Receiving Standard of Care Treatment |
| 2027-08-01 | US | VRCA | Verrica Pharmaceuticals Inc. | Phase 3 | Cantharidin Application in Patients With Common Warts (Verruca Vulgaris) (COVE-3) |
| 2027-08-01 | US | ZJYL | Jin Medical International Ltd. | Phase 2 | Investigator Initiated Study for the Safety and Efficacy in Frontotemporal Dementia |
| 2027-08-01 | US | ZLAB | Zai Lab Limited | Phase 2 | A Study of ZL-1310 in Participants With Selected Solid Tumors |
| 2027-08-10 | US | LCTX | Lineage Cell Therapeutics, Inc. | Phase 1 | A Study to Evaluate the Safety of a Delivery Device for Administering LCTOPC1 in Participants With Spinal Cord Injury |
| 2027-08-16 | US | VIR | Vir Biotechnology, Inc. | Phase 2 | To Access the Safety and Effects of Intravenous Administration of VIR-5818 Alone and in Combination With Pembrolizumab in Adult Participants With Locally Advanced or Metastatic HER2-Expressing Cancers |
| 2027-08-16 | US | VSTM | Verastem, Inc. | Phase 2 | A Study of Avutometinib and Defactinib in People With Thyroid Cancer |
| 2027-08-27 | US | PMVP | PMV Pharmaceuticals, Inc. | Phase 1 | A Phase Ib Study of Rezatapopt in Combination With Azacitidine in Patients With TP53Y220C Mutant Myeloid Malignancies (Acute Myeloid Leukemia or Myelodysplastic Syndrome) |
| 2027-08-29 | US | NVCR | NovoCure Limited | Phase 2 | A Study of NovoTTF-200T(P) in Combination With Gemcitabine and Nab-Paclitaxel for Resectable Pancreatic Adenocarcinoma |
| 2027-08-30 | US | LNTH | Lantheus Holdings, Inc. | Phase 1 | A Phase 1, Multicenter Imaging Study of LNTH-2403 in Participants With Locally Advanced or Metastatic Solid Tumors. |
| 2027-08-30 | US | RADX | Radiopharm Theranostics Limited | Phase 1 | A Phase 1, Multicenter Imaging Study of LNTH-2403 in Participants With Locally Advanced or Metastatic Solid Tumors. |
| 2027-08-31 | US | CRDF | Cardiff Oncology, Inc. | Phase 2 | Study of PLK1 Inhibitor, Onvansertib, in Relapsed Small Cell Lung Cancer |
| 2027-08-31 | US | IART | Integra LifeSciences Holdings Corporation | Phase 2 | Human Amnion Membrane Allograft and Early Return of Erectile Function After Radical Prostatectomy |
| 2027-08-31 | US | MIRM | Mirum Pharmaceuticals, Inc. | Phase 3 | Study to Evaluate Switching to Brelovitug for the Treatment of CHD in Participants Receiving Bulevirtide |
| 2027-08-31 | US | RIGL | Rigel Pharmaceuticals, Inc. | Phase 2 | A Phase 2 Study Evaluating Olutasidenib in Patients With IDH1-mutated Clonal Cytopenia of Undetermined Significance and Lower-risk Myelodysplastic/Syndromes/Chronic Myelomonocytic Leukemia. |
| 2027-08-31 | US | TLX | Telix Pharmaceuticals Limited | Phase 3 | Phase 3 Study to Assess Safety and Efficacy of 177Lu-TLX250 in Advanced Relapsed or Recurrent ccRCC |
| 2027-09-01 | US | AGEN | Agenus Inc. | Phase 2 | A Study of Botensilimab and Balstilimab for the Treatment of Colorectal Cancer |
| 2027-09-01 | US | BHVN | Biohaven Ltd. | Phase 1 | Study of BHV-1300 in Graves' Disease |
| 2027-09-01 | US | CHRS | Coherus Oncology, Inc. | Phase 2 | A Trial of Casdozokitug in Combination With Toripalimab Plus Bevacizumab in Participants With Unresectable and/or Locally Advanced or Metastatic Hepatocellular Carcinoma |
| 2027-09-01 | US | CLYM | Climb Bio Inc | Phase 2 | A Phase 1b/2a Study of Budoprutug in Systemic Lupus Erythematosus (SLE) |
| 2027-09-01 | US | CORT | Corcept Therapeutics Incorporated | Phase 2 | Relacorilant With Nab-Paclitaxel and Gemcitabine in Patients With Metastatic Pancreatic Adenocarcinoma |
| 2027-09-01 | US | CORT | Corcept Therapeutics Incorporated | Phase 2 | Relacorilant With Nab-Paclitaxel and Gemcitabine in Patients With Metastatic Pancreatic Adenocarcinoma |
| 2027-09-01 | US | CSTL | Castle Biosciences, Inc. | Phase 3 | Evaluation of D-Fi for the Treatment of Wounds Due to DEB |
| 2027-09-01 | US | HUMA | Humacyte, Inc. | Phase 3 | Humacyte Human Acellular Vessel (HAV) in Patients With Vascular Trauma |
| 2027-09-01 | US | IMTX | Immatics N.V. | Phase 2 | IMA402 T Cell-Engaging Receptor Molecule (TCER®) in Recurrent and/or Refractory Solid Tumors |
| 2027-09-01 | US | IOVA | Iovance Biotherapeutics, Inc. | Phase 2 | A Study to Investigate the Efficacy and Safety of an Infusion of IOV-4001 in Adult Participants With Unresectable or Metastatic Melanoma or Stage III or IV Non-small-cell Lung Cancer |
| 2027-09-01 | US | KTTA | Pasithea Therapeutics Corp. | Phase 1 | PAS-004 in Adults Who Have Neurofibromatosis Type 1 With Plexiform Neurofibromas |
| 2027-09-01 | US | KYTX | Kyverna Therapeutics, Inc. | Phase 3 | KYSA-6: A Study of Anti-CD19 Chimeric Antigen Receptor T-Cell Therapy, in Patients With Generalized Myasthenia Gravis |
| 2027-09-01 | US | NEO | NeoGenomics, Inc. | Phase 2 | Molecular Residual Disease Interception in Locoregionally-Advanced High Risk HPV+ and HPV- HNSCC |
| 2027-09-01 | US | RARE | Ultragenyx Pharmaceutical Inc. | Phase 3 | Clinical Study of DTX301 AAV-Mediated Gene Transfer for Ornithine Transcarbamylase (OTC) Deficiency |
| 2027-09-01 | US | RCUS | Arcus Biosciences, Inc. | Phase 1 | Study of AB598 Monotherapy and Combination Therapy in Participants With Advanced Cancers |
| 2027-09-01 | US | RZLT | Rezolute, Inc. | Phase 3 | A Phase 3 Study of Ersodetug in Patients With Tumor Hyperinsulinism |
| 2027-09-01 | US | TLSI | TriSalus Life Sciences, Inc. | Phase 1 | Pressure Enabled Intrapancreatic Delivery of SD-101 With Checkpoint Blockade for Locally Advanced Pancreatic Adenocarcinoma |
| 2027-09-01 | US | UPB | Upstream Bio, Inc. | Phase 2 | A Long-Term Safety and Efficacy Study of Verekitug (UPB-101) in Adult Participants With Severe Asthma (VALOUR) |
| 2027-09-01 | Ex-US | VACBF | Nykode Therapeutics AS | Phase 2 | Safety and Efficacy of VB10.16 and Pembrolizumab in Patients with Head-Neck Squamous Cell Carcinoma |
| 2027-09-01 | US | XFOR | X4 Pharmaceuticals, Inc. | Phase 3 | A Study of Mavorixafor in Participants With Congenital and Acquired Primary Autoimmune and Idiopathic Chronic Neutropenic Disorders Who Are Experiencing Recurrent and/or Serious Infections |
| 2027-09-01 | US | ZYME | Zymeworks Inc. | Phase 1 | A Study of ZW251 in Participants With Advanced Solid Tumors |
| 2027-09-29 | US | ADPT | Adaptive Biotechnologies Corporation | Phase 2 | MRD Guided De-intensification of Bendamustine/Rituximab for Indolent Non-Hodgkin Lymphoma |
| 2027-09-29 | US | VIR | Vir Biotechnology, Inc. | Phase 1 | Safety, Pharmacokinetics, and Preliminary Efficacy of VIR-5500 (AMX-500) in Prostate Cancer |
| 2027-09-30 | US | CNTA | Centessa Pharmaceuticals plc | Phase 3 | A Study to Investigate the Effects of Cleminorexton Compared With Placebo in the Treatment of Participants With Central Disorders of Hypersomnolence |
| 2027-09-30 | US | FATE | Fate Therapeutics, Inc. | Phase 1 | A Phase 1 Study of FT819 in B-cell Mediated Autoimmune Disease |
| 2027-09-30 | US | IMCR | Immunocore Holdings plc | Phase 1 | Study of IMC-P115C in Advanced PRAME-Positive Cancers |
| 2027-09-30 | US | IVA | Inventiva S.A. | Phase 3 | A Phase 3 Study Evaluating Efficacy and Safety of Lanifibranor Followed by an Active Treatment Extension in Adult Patients With MASH and Fibrosis Stages F2 and F3 (NATiV3) |
| 2027-09-30 | US | LEGN | Legend Biotech Corporation | Phase 1 | A Study of LCAR-AIO in Subjects With Relapsed/Refractory Systemic Lupus Erythematosus |
| 2027-09-30 | US | MAIA | MAIA Biotechnology, Inc. | Phase 2 | THIO Sequenced With Cemiplimab in Advanced NSCLC |
| 2027-09-30 | US | RNTX | Rein Therapeutics Inc. | Phase 2 | A Phase 2 Study of LTI-03 in Patients With Idiopathic Pulmonary Fibrosis |
| 2027-09-30 | US | VNDA | Vanda Pharmaceuticals Inc. | Phase 3 | Motion Delos: An Open Label Safety and Efficacy of Tradipitant in Participants Affected by Motion Sickness |
| 2027-09-30 | US | VNDA | Vanda Pharmaceuticals Inc. | Phase 3 | Motion Delos: An Open Label Safety and Efficacy of Tradipitant in Participants Affected by Motion Sickness |
| 2027-10-01 | US | AGEN | Agenus Inc. | Phase 2 | A Study of Evofosfamide in Combination with Zalifrelimab and Balstilimab |
| 2027-10-01 | US | APVO | Aptevo Therapeutics Inc. | Phase 1 | APVO436 Phase 1b/2 Study in Patients With Newly Diagnosed AML |
| 2027-10-01 | US | CERS | Cerus Corporation | Phase 2 | Challenge Transfusion of INTERCEPT Pathogen Reduced Red Blood Cells (RBCs) in Subjects With or Without Pre-existing Antibodies to INTERCEPT RBCs |
| 2027-10-01 | US | CLYM | Climb Bio Inc | Phase 2 | A Phase 2 Study of Budoprutug in Subjects With Primary Membranous Nephropathy |
| 2027-10-01 | US | CORT | Corcept Therapeutics Incorporated | Phase 2 | A Study of Enzalutamide, Enzalutamide in Combination With Mifepristone, or Chemotherapy in People With Metastatic Breast Cancer |
| 2027-10-01 | US | CORT | Corcept Therapeutics Incorporated | Phase 2 | A Study of Enzalutamide, Enzalutamide in Combination With Mifepristone, or Chemotherapy in People With Metastatic Breast Cancer |
| 2027-10-01 | US | EVMN | Evommune, Inc. | Phase 2 | Study of EVO756 in Adults With Migraine |
| 2027-10-01 | US | EYPT | EyePoint, Inc. | Phase 3 | CAPRI: A Phase 3 Randomized, Double-Masked Study Comparing the Efficacy of EYP-1901 Against Aflibercept in DME |
| 2027-10-01 | US | EYPT | EyePoint, Inc. | Phase 3 | COMO: A Phase 3 Randomized, Double-Masked Study Comparing the Efficacy of EYP-1901 Against Aflibercept in DME |
| 2027-10-01 | US | JBIO | Jade Biosciences, Inc. | Phase 1 | A Phase 1 Study of JADE201 in Participants With Rheumatoid Arthritis |
| 2027-10-01 | US | MIRM | Mirum Pharmaceuticals, Inc. | Phase 2 | Study of MRM-3379 in Male Participants With Fragile X Syndrome (BLOOM) |
| 2027-10-01 | US | NVCR | NovoCure Limited | Phase 2 | Nab-Paclitaxel + Cisplatin + Gemcitabine + TTF in pt. w/ Metastatic PAC |
| 2027-10-01 | US | OGN | Organon & Co. | Phase 2 | Evaluating Pembrolizumab, Trastuzumab and FLOT as Perioperative Treatment of HER2-positive, Localized Esophagogastric Adenocarcinoma |
| 2027-10-01 | US | OPK | OPKO Health, Inc. | Phase 2 | Pharmacokinetics, Pharmacodynamics, Safety and Tolerability Evaluation of CTAP101 Extended-release Capsules in Pediatric Participants |
| 2027-10-01 | US | ORKA | Oruka Therapeutics, Inc. | Phase 2 | Dose Ranging Study of ORKA-002 in Patients With Moderate-to-Severe Plaque Psoriasis |
| 2027-10-16 | US | IMCR | Immunocore Holdings plc | Phase 3 | IMC-F106C Regimen Versus Nivolumab Regimens in Previously Untreated Advanced Melanoma (PRISM-MEL-301) |
| 2027-10-20 | Ex-US | KNTPF | Kintor Pharmaceutical Limited | Phase 3 | To Evaluate Efficacy and Safety of TopicalKX-826 Solution in Chinese Male Patients With Androgenetic Alopecia |
| 2027-10-23 | Ex-US | SYMQY | SymBio Pharmaceuticals Limited | Phase 2 – Suspended | A Phase 1b/2 Study of Intravenous Brincidofovir in Patients With Relapsed or Refractory Lymphoma and Relapsed or Refractory Extranodal Natural Killer/T-cell Lymphoma |
| 2027-10-26 | Ex-US | GSGTF | GenSight Biologics S.A. | Phase 2 | Dose-escalation Study to Evaluate the Safety and Tolerability of GS030 in Subjects With Retinitis Pigmentosa |
| 2027-10-30 | US | PBYI | Puma Biotechnology, Inc. | Phase 2 | A Study of Alisertib in Patients With Extensive Stage Small Cell Lung Cancer |
| 2027-10-30 | US | TFX | Teleflex Incorporated | Phase 1 | Hyaluronic Acid-based Gel Spacers in Gynecologic Malignancies |
| 2027-10-30 | US | TLX | Telix Pharmaceuticals Limited | Phase 2 | Phase 1b/2 Study of Combination 177Lu Girentuximab Plus Cabozantinib and Nivolumab in Treatment naïve Patients With Advanced Clear Cell RCC |
| 2027-10-31 | US | CUE | Cue Biopharma, Inc. | Phase 2 | Three Schedules of CUE-101 Administered Before Surgery or Definitive Chemoradiation Therapy in HLA-A*0201 Positive Patients With Locally Advanced, HPV16-Positive Oropharyngeal Squamous-Cell Carcinoma |
| 2027-10-31 | Ex-US | JCRRF | JCR Pharmaceuticals Co., Ltd. | Phase 3 | A Phase III Study of JR-141 in Patients With Mucopolysaccharidosis II (STARLIGHT) |
| 2027-10-31 | US | LXRX | Lexicon Pharmaceuticals, Inc. | Phase 2 | Sotagliflozin in Patients With Heart Failure Symptoms and Type 1 Diabetes |
| 2027-10-31 | Ex-US | NURPF | Neuren Pharmaceuticals Limited | Phase 3 | A Study of NNZ-2591 in Pediatric Participants With Phelan-McDermid Syndrome |
| 2027-11-01 | US | CHRS | Coherus Oncology, Inc. | Phase 2 | A Combination Therapy Strategy to Prevent Anti-PD-1 Therapy Resistance in Metastatic Ovarian Cancer Patients |
| 2027-11-01 | US | CRIS | Curis, Inc. | Phase 2 | A Study of Emavusertib + An Approved Bruton Tyrosine Kinase Inhibitor (BTKi) in Participants With Chronic Lymphocytic Leukemia (CLL) and Other B-cell Malignancies |
| 2027-11-01 | US | CRVS | Corvus Pharmaceuticals, Inc. | Phase 3 | Soquelitinib vs Standard of Care in Participants With Relapsed/Refractory Peripheral T-cell Lymphoma Not Otherwise Specified, Follicular Helper T-cell Lymphomas, or Systemic Anaplastic Large-cell Lymphoma |
| 2027-11-01 | US | DVAX | Dynavax Technologies Corporation | Phase 2 | Safety and Immunogenicity of an Investigational Herpes Zoster Vaccine (Z-1018) Compared to Shingrix® in Healthy Adults 50 Years of Age and Over |
| 2027-11-01 | Ex-US | JBPHF | Jacobio Pharmaceuticals Group Co., Ltd. | Phase 2 | JAB-23E73 in Adult Participants With Advanced Solid Tumors With KRAS Alteration |
| 2027-11-01 | Ex-US | KSPHF | Kissei Pharmaceutical Co., Ltd. | Phase 3 | A Clinical Study of KLH-2109 in Patients With Endometriosis |
| 2027-11-01 | US | MPLT | MapLight Therapeutics, Inc. | Phase 2 | ML-004 Open-Label Extension Study in Adults and Adolescents With Autism Spectrum Disorders (ASD) |
| 2027-11-01 | US | NAMS | NewAmsterdam Pharma Company N.V. | Phase 3 | A CCTA Imaging Trial to Evaluate the Effect of Obicetrapib/Ezetimibe on Coronary Plaque |
| 2027-11-01 | US | REPL | Replimune Group, Inc. | Phase 2 | Neoadjuvant Intra-tumoral RP2 and FLOT in Gastroesophageal Adenocarcinoma |
| 2027-11-01 | US | REPL | Replimune Group, Inc. | Phase 2 | Neoadjuvant Intra-tumoral RP2 and FLOT in Gastroesophageal Adenocarcinoma |
| 2027-11-01 | US | SABS | SAB Biotherapeutics, Inc. | Phase 2 | SAFety and Efficacy of Human Anti-thymocyte ImmunoGlobUlin SAB-142 ARresting Progression of Type 1 Diabetes |
| 2027-11-01 | US | VERA | Vera Therapeutics, Inc. | Phase 2 | Atacicept in Multiple Glomerular Diseases |
| 2027-11-01 | US | VERA | Vera Therapeutics, Inc. | Phase 2 | Atacicept in Multiple Glomerular Diseases |
| 2027-11-01 | US | VNDA | Vanda Pharmaceuticals Inc. | Phase 3 | Evaluating the Effects of Tasimelteon vs. Placebo in Treating Pediatric Insomnia |
| 2027-11-01 | US | VNDA | Vanda Pharmaceuticals Inc. | Phase 3 | Randomized Withdrawal Study in Patients With Schizophrenia |
| 2027-11-01 | US | VNDA | Vanda Pharmaceuticals Inc. | Phase 3 | Evaluating the Effects of Tasimelteon vs. Placebo in Treating Pediatric Insomnia |
| 2027-11-01 | US | VNDA | Vanda Pharmaceuticals Inc. | Phase 3 | Randomized Withdrawal Study in Patients With Schizophrenia |
| 2027-11-15 | US | AURA | Aura Biosciences, Inc. | Phase 3 | A Phase 3 Randomized, Masked, Controlled Trial to Evaluate Efficacy and Safety of Belzupacap Sarotalocan (AU-011) Treatment Compared to Sham Control in Subjects With Primary Indeterminate Lesions or Small Choroidal Melanoma |
| 2027-11-19 | US | LNTH | Lantheus Holdings, Inc. | Phase 2 | Prostate Specific Membrane Antigen (PMSA)-Based PET Imaging of High Risk Prostate Cancer |
| 2027-11-19 | US | LNTH | Lantheus Holdings, Inc. | Phase 2 | Prostate Specific Membrane Antigen (PMSA)-Based PET Imaging of High Risk Prostate Cancer |
| 2027-11-22 | US | CGEN | Compugen Ltd. | Phase 1 | A Clinical Trial to Assess COM503 in Participants With Advanced Solid Malignancies |
| 2027-11-30 | US | ARVN | Arvinas, Inc. | Phase 2 | A Study to Evaluate ARV-806 in Adults With Advanced Cancer That Has the KRAS G12D Mutation |
| 2027-11-30 | US | CTMX | CytomX Therapeutics, Inc. | Phase 1 | First In Human Study of CX-2051 in Advanced Solid Tumors |
| 2027-11-30 | Ex-US | FGHQF | Frontage Holdings Corporation | Phase 2 | SKB264 in Combination With Pembrolizumab in Subjects With Selected Solid Tumors |
| 2027-11-30 | US | MYGN | Myriad Genetics, Inc. | Phase 2 | SKB264 in Combination With Pembrolizumab in Subjects With Selected Solid Tumors |
| 2027-11-30 | US | SRPT | Sarepta Therapeutics, Inc. | Phase 1 | A First-in-human Study of the Effects of SRP-1005 in Participants With Huntington's Disease |
| 2027-11-30 | US | ZJYL | Jin Medical International Ltd. | Phase 3 | Desiccated Thyroid Extract Combined With Levothyroxine for TSH Suppression Therapy in DTC |
| 2027-12-01 | Ex-US | ABSCF | AB Science S.A. | Phase 3 | Efficacy and Safety of Masitinib Versus Placebo in the Treatment of ALS Patients |
| 2027-12-01 | US | ADAG | Adagene Inc. | Phase 2 | A Phase Ib Safety lead-in, Followed by Phase II Trial of ADG106 in Combination With Neoadjuvant Chemotherapy in HER2 Negative Breast Cancer |
| 2027-12-01 | US | AKTS | Aktis Oncology, Inc. | Phase 1 | A Study of [225Ac]Ac-AKY-1189 in Patients With Solid Tumors |
| 2027-12-01 | US | AKTS | Aktis Oncology, Inc. | Phase 1 | A Study of [225Ac]Ac-AKY-2519 in Patients With Metastatic Castration-Resistant Prostate Cancer |
| 2027-12-01 | US | ALLO | Allogene Therapeutics, Inc. | Phase 2 | Consolidation of First-Line MRD+ Remission With Cema-cel in Patients With LBCL |
| 2027-12-01 | US | ALXO | ALX Oncology Holdings Inc. | Phase 2 | ASPEN-09-03: A Study of Evorpacept in Combination With Trastuzumab and Chemotherapy in Metastatic HER2-Positive Breast Cancer |
| 2027-12-01 | US | ANTX | AN2 Therapeutics, Inc. | Phase 2 | Epetraborole in Patients With Mycobacterium Abscessus Lung Disease |
| 2027-12-01 | US | ANVS | Annovis Bio, Inc. | Phase 3 | A Double-blind Dual Study Assessing Safety and Efficacy of Buntanetap in Participants With Early AD |
| 2027-12-01 | Ex-US | ASPHF | Ascentage Pharma Group International | Phase 1 | APG-2449 in Patients With Advanced Solid Tumors |
| 2027-12-01 | US | BCTX | BriaCell Therapeutics Corp. | Phase 3 | Study of the Bria-IMT Regimen and CPI vs Physicians' Choice in Advanced Metastatic Breast Cancer. |
| 2027-12-01 | US | CANF | Can-Fite BioPharma Ltd. | Phase 3 | A Phase 3 Study in Moderate-to-Severe Plaque Psoriasis With Piclidenoson to Study Safety and Efficacy |
| 2027-12-01 | US | CRBU | Caribou Biosciences, Inc. | Phase 1 | CRISPR-Edited Allogeneic Anti-BCMA CAR-T Cell Therapy in Patients With Relapsed/Refractory Multiple Myeloma |
| 2027-12-01 | US | DAWN | Day One Biopharmaceuticals, Inc. | Phase 1 | To Evaluate the Safety, Tolerability, Pharmacokinetics and Antitumor Activity of DAY301 in Participants With Locally Advanced or Metastatic Solid Tumors |
| 2027-12-01 | US | DNLI | Denali Therapeutics Inc. | Phase 3 | A Study to Determine the Efficacy and Safety of Tividenofusp Alfa (DNL310) vs Idursulfase in Pediatric and Young Adult Participants With Neuronopathic (nMPS II) or Non-Neuronopathic Mucopolysaccharidosis Type II (nnMPS II) |
| 2027-12-01 | US | ELVN | Enliven Therapeutics, Inc. | Phase 1 | A Phase 1a/1b Study of ELVN-001 for the Treatment Chronic Myeloid Leukemia |
| 2027-12-01 | US | FOLD | Amicus Therapeutics, Inc. | Phase 3 | A Study of Migalastat in Pediatric Subjects (2 to <12 Yrs) With Fabry Disease and Amenable GLA Variants |
| 2027-12-01 | US | GOSS | Gossamer Bio, Inc. | Phase 2 | Open-label Extension Study of GB002 in Adult Subjects With Pulmonary Arterial Hypertension (PAH) |
| 2027-12-01 | Ex-US | INCPF | InnoCare Pharma Limited | Phase 2 | A Study to Evaluate the Efficacy and Safety of ICP-248 in Subjects With Relapsed or Refractory Mantle Cell Lymphoma (APEX-06) |
| 2027-12-01 | US | INTS | Intensity Therapeutics, Inc. | Phase 3 | A Study to Investigate Efficacy & Safety of Intratumoral INT230-6 Compared to US Standard of Care in Adults With Soft Tissue Sarcomas (INVINCIBLE-3) |
| 2027-12-01 | US | KURA | Kura Oncology, Inc. | Phase 1 | A Study of Ziftomenib in Combination With Imatinib in Patients With Advanced Gastrointestinal Stromal Tumors (GIST) |
| 2027-12-01 | US | LEGN | Legend Biotech Corporation | Phase 1 | Claudin 18.2-Targeted Chimeric Antigen Receptor T-cells in Subjects With Unresectable, Locally Advanced, or Metastatic Gastric, Gastroesophageal Junction (GEJ), Esophageal, or Pancreatic Adenocarcinoma |
| 2027-12-01 | US | LEGN | Legend Biotech Corporation | Phase 1 | DLL3-Directed Chimeric Antigen Receptor T-cells in Subjects With Extensive Stage Small Cell Lung Cancer |
| 2027-12-01 | Ex-US | MDGEF | Medigene AG | Phase 1 | EPITOME-1015-I: a Study to Investigate the Safety and Tolerability of MDG1015 in Patients with Epithelial Ovarian Cancer, Gastroesophageal Adenocarcinoma, Round Cell Liposarcoma And/or Synovial Sarcoma |
| 2027-12-01 | US | MPLT | MapLight Therapeutics, Inc. | Phase 2 | A Study to Assess the Efficacy and Safety of ML-007C-MA for the Treatment of Alzheimer's Disease Psychosis |
| 2027-12-01 | US | NTLA | Intellia Therapeutics, Inc. | Phase 3 | MAGNITUDE: A Phase 3 Study of NTLA-2001 in Participants With Transthyretin Amyloidosis With Cardiomyopathy (ATTR-CM) |
| 2027-12-01 | US | OPK | OPKO Health, Inc. | Phase 2 | Phase 1/2 Study of OPK-88006 in Healthy and Presumed MASH Participants |
| 2027-12-01 | US | QURE | uniQure N.V. | Phase 2 | Safety, PK/PD, and Exploratory Efficacy Study of AMT-191 in Classic Fabry Disease |
| 2027-12-01 | US | RADX | Radiopharm Theranostics Limited | Phase 1 | HEAT Trial (HER2 Antibody Therapy With Lutetium-177) |
| 2027-12-01 | US | RADX | Radiopharm Theranostics Limited | Phase 2 | 177Lu-BetaBart in Patients With Relapsed/Refractory, Locally Advanced Inoperable, or Metastatic Solid Tumors |
| 2027-12-01 | US | RARE | Ultragenyx Pharmaceutical Inc. | Phase 2 | Study to Evaluate the Use of Triheptanoin in Patients With Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCADD) |
| 2027-12-01 | US | RCUS | Arcus Biosciences, Inc. | Phase 2 | Study With Various Immunotherapy Treatments in Participants With Lung Cancer |
| 2027-12-01 | US | REPL | Replimune Group, Inc. | Phase 2 | Study of RP2 in Combination With Second-line Therapy in Patients With Locally Advanced or Metastatic HCC |
| 2027-12-01 | US | REPL | Replimune Group, Inc. | Phase 2 | Study of RP2 in Combination With Second-line Therapy in Patients With Locally Advanced or Metastatic HCC |
| 2027-12-01 | US | RGNX | REGENXBIO Inc. | Phase 2 | Phase 2 Trial of RGX-314 in Adults With Center Involved – Diabetic Macular Edema (CI – DME) |
| 2027-12-01 | US | RGNX | REGENXBIO Inc. | Phase 2 | Phase 2 Trial of RGX-314 in Adults With Center Involved – Diabetic Macular Edema (CI – DME) |
| 2027-12-01 | US | RIGL | Rigel Pharmaceuticals, Inc. | Phase 1 | Perioperative Fostamatinib With Gemcitabine and Nab-paclitaxel in Resectable Pancreatic Cancer |
| 2027-12-01 | US | RNAC | Cartesian Therapeutics, Inc. | Phase 2 | Descartes-08 for Children, Adolescents, and Young Adults With Autoimmune Disorders |
| 2027-12-01 | US | RPTX | Repare Therapeutics Inc. | Phase 1 | Study of Lunresertib Alone or in Combination With RP-3500 or Debio 0123 in Patients With Advanced Solid Tumors |
| 2027-12-01 | US | SANA | Sana Biotechnology, Inc. | Phase 1 | Study Evaluating SC291 in Subjects With Severe r/r B-cell Mediated Autoimmune Diseases (GLEAM) |
| 2027-12-01 | US | STRO | Sutro Biopharma, Inc. | Phase 1 | A Study of STRO-004 in Adults With Refractory/Recurrent Metastatic Cancer |
| 2027-12-01 | US | TGTX | TG Therapeutics, Inc. | Phase 3 | Study to Evaluate Safety, Efficacy and Pharmacokinetics (PK) of a Modified Regimen of Ublituximab |
| 2027-12-01 | US | TGTX | TG Therapeutics, Inc. | Phase 1 | A Study to Assess the Safety and Clinical Activity of Azer-cel in Participants With B-cell Mediated Autoimmune Disorders |
| 2027-12-01 | US | TLX | Telix Pharmaceuticals Limited | Phase 3 | The Study of 177Lu-TLX591 Plus SOC Versus SOC Alone in Patients With mCRPC (ProstACT Global) |
| 2027-12-01 | US | VSTM | Verastem, Inc. | Phase 2 | A Phase 2 Study of Avutometinib (VS-6766) Plus Defactinib |
| 2027-12-01 | US | WVE | Wave Life Sciences Ltd. | Phase 2 | A Phase 1/2a Study of WVE-007 in Adults Living With Overweight or Obesity |
| 2027-12-01 | US | XNCR | Xencor, Inc. | Phase 1 | Phase 1, Safety and Tolerability Study of XmAb541 in Advanced Solid Tumors |
| 2027-12-01 | US | ZJYL | Jin Medical International Ltd. | Phase 3 | Mecobalamin in Promoting Recurrent Laryngeal Nerve Function Recovery After Thyroid Surgery |
| 2027-12-06 | US | PYXS | Pyxis Oncology, Inc. | Phase 2 | Phase 1/2 Study of PYX-201 in Combination With Pembrolizumab in Advanced Solid Tumors |
| 2027-12-15 | Ex-US | ORPOF | OSE IMMUNOTHERAPEUTICS | Phase 3 | Trial of Therapeutic Cancer Vaccine OSE2101 in Patients With Non-Small Cell Lung Cancer and Secondary Resistance to Immune Checkpoint Inhibitor |
| 2027-12-15 | US | SNDX | Syndax Pharmaceuticals, Inc. | Phase 2 | A Study of Revumenib in R/R Leukemias Including Those With an MLL/KMT2A Gene Rearrangement or NPM1 Mutation |
| 2027-12-25 | Ex-US | INCPF | InnoCare Pharma Limited | Phase 2 | Study of ICP-723 in Patients With Advanced Solid Tumors or Primary Central Nervous System Tumors |
| 2027-12-27 | US | MBRX | Moleculin Biotech, Inc. | Phase 2 | WP1066 and Radiation Therapy in Treating Patients With Newly Diagnosed Glioblastoma |
| 2027-12-28 | US | ZLAB | Zai Lab Limited | Phase 1 | A Phase 1/1b Study to Evaluate Safety, Tolerability and Pharmacokinetics of ZL-1503 in Healthy Volunteers and Participants With Moderate to Severe Atopic Dermatitis |
| 2027-12-30 | US | BEAM | Beam Therapeutics Inc. | Phase 2 | A Phase 1/2, Dose-Exploration Study to Evaluate the Safety and Efficacy of BEAM-301 in Patients With Glycogen Storage Disease Type Ia (GSDIa) |
| 2027-12-30 | US | CGEM | Cullinan Therapeutics, Inc. | Phase 1 | A Study of CLN-978, a Subcutaneously Administered CD19-directed T Cell Engager, in Subjects With Rheumatoid Arthritis |
| 2027-12-30 | US | MDWD | MediWound Ltd. | Phase 2 | Clinical Study to Evaluate the Safety and the Efficacy of EscharEx Drug Product (EX-03 Formulation) and Its Placebo Compared to Collagenase, Non-surgical Standard of Care, in Patients With Venous Leg Ulcers |
| 2027-12-30 | US | RLAY | Relay Therapeutics, Inc. | Phase 1 | A First-in-human Study of RLY-8161 in Advanced NRAS-Mutant Solid Tumors |
| 2027-12-30 | Ex-US | TRGNF | Transgene SA | Phase 2 | A Clinical Trial Evaluating TG4050 in Head and Neck Cancer |
| 2027-12-31 | US | ADAG | Adagene Inc. | Phase 2 | Neoadjuvant ADG126 and Pembrolizumab in Locally Advanced Colorectal Cancer |
| 2027-12-31 | Ex-US | ASPHF | Ascentage Pharma Group International | Phase 1 | A Study to Evaluate the Safety, Pharmacokinetics and Preliminary Efficacy of APG-5918. |
| 2027-12-31 | US | CATX | Perspective Therapeutics, Inc. | Phase 2 | MC1R-targeted Alpha-particle Monotherapy and Combination Therapy Trial With Nivolumab in Adults With Advanced Melanoma |
| 2027-12-31 | US | CHRS | Coherus Oncology, Inc. | Phase 2 | PDT For Induction Therapy For Head And Neck Cancer |
| 2027-12-31 | US | CLDX | Celldex Therapeutics, Inc. | Phase 1 | NeoVax + CDX-301 and Nivolumab or Pembrolizumab in Melanoma |
| 2027-12-31 | US | KNSA | Kiniksa Pharmaceuticals International, plc | Phase 3 | Phase 2/3 Study of KPL-387 in Recurrent Pericarditis |
| 2027-12-31 | US | KNSA | Kiniksa Pharmaceuticals International, plc | Phase 2 | Transition to KPL-387 Monotherapy Dosing & Administration Study |
| 2027-12-31 | US | KURA | Kura Oncology, Inc. | Phase 2 | Ziftomenib for the Treatment of Patients With NPM1 Mutated or KMT2A Rearranged Acute Myeloid Leukemia Not Eligible for Standard Therapy |
| 2027-12-31 | Ex-US | LYPHF | Luye Pharma Group Ltd. | Phase 3 | Lurbinectedin or in Combination with Irinotecan Versus Topotecan in Patients with Relapsed SCLC |
| 2027-12-31 | Ex-US | LYPHF | Luye Pharma Group Ltd. | Phase 2 | A Phase 2 Study to Evaluate the Efficacy and Safety of LY03020 in Acutely Psychotic Participants With Schizophrenia |
| 2027-12-31 | US | NKTR | Nektar Therapeutics | Phase 2 | REStoring lymphoCytes Using NKTR-255* After chemoradiothErapy in Solid Tumors (RESCUE) |
| 2027-12-31 | US | NUVL | Nuvalent, Inc. | Phase 1 | A Study of Zidesamtinib (NVL-520) in Patients With Advanced NSCLC and Other Solid Tumors Harboring ROS1 Rearrangement (ARROS-1) |
| 2027-12-31 | US | OLMA | Olema Pharmaceuticals, Inc. | Phase 1 | Phase 1b Study of OP-1250 (Palazestrant) in Combination With Ribociclib, Alpelisib, Everolimus, or Atirmociclib in ER+, HER2- Breast Cancer |
| 2027-12-31 | US | SRPT | Sarepta Therapeutics, Inc. | Phase 1 | A Gene Transfer Therapy Study to Evaluate the Safety of and Expression From Delandistrogene Moxeparvovec (SRP-9001) in Participants With Duchenne Muscular Dystrophy (DMD) – Non-Ambulatory Cohort |
| 2027-12-31 | US | SUPN | Supernus Pharmaceuticals, Inc. | Phase 2 | SPN-817 Open-Label Extension Study in Adults With Focal Onset Seizures |
| 2027-12-31 | US | VSTM | Verastem, Inc. | Phase 2 | VS-6766+Abema+Fulv in Met HR+/HER- BC |
| 2028-01-01 | US | ACAD | ACADIA Pharmaceuticals Inc. | Phase 3 | ACP-204 in Adults With Alzheimer's Disease Psychosis |
| 2028-01-01 | US | ACIU | AC Immune SA | Phase 2 | A Study to Evaluate the Effects of ACI-7104.056 in Patients With Early Stages of Parkinson's Disease |
| 2028-01-01 | US | ARTV | Artiva Biotherapeutics, Inc. | Phase 2 | AlloNK®, an Allogeneic Non-genetically Modified, Cord Blood-derived NK Cell Therapy, in Combination With Rituximab, Studied in Relapsing Forms of B-cell Dependent Rheumatologic Diseases. |
| 2028-01-01 | US | BHVN | Biohaven Ltd. | Phase 3 | Study to Determine if BHV-1300 is Effective and Safe in Adults With Graves' Disease |
| 2028-01-01 | US | BLRX | BioLineRx Ltd. | Phase 1 | SCD Stem Cell Mobilization and Apheresis Using Motixafortide |
| 2028-01-01 | US | CELC | Celcuity Inc. | Phase 2 | Gedatolisib in Combination With Darolutamide in Metastatic Castration-Resistant Prostate Cancer |
| 2028-01-01 | US | CHRS | Coherus Oncology, Inc. | Phase 1 | A Study of CHS-114 (Tagmokitug) in Combination With Toripalimab and/or Other Treatments in Participants With Advanced Solid Tumors |
| 2028-01-01 | US | CRMD | CorMedix Inc. | Phase 3 | Comparing The Safety And Efficacy Of DEFENCATH® In Reducing Central-Line Bloodstream Infections (CLABSIs) In Adults Receiving Total Parenteral Nutrition Through A Central Venous Catheter (CVC) |
| 2028-01-01 | Ex-US | CSPHF | CStone Pharmaceuticals | Phase 1 | A Phase I Study of CS5007 in Participants With Advanced Solid Tumors |
| 2028-01-01 | US | CYDY | CytoDyn Inc. | Phase 2 | The Phase-2 CCR5-targeting Leronlimab With Oral Chemotherapy and VEGF-inhibitor Enriched Regimen Trial (CLOVER) |
| 2028-01-01 | US | ELVN | Enliven Therapeutics, Inc. | Phase 1 | ELVN-001 for the Treatment of Chronic Myeloid Leukemia With and Without T315I Mutation in Japanese Participants |
| 2028-01-01 | US | FATE | Fate Therapeutics, Inc. | Phase 1 | FT836 With or Without Chemotherapy and/or Monoclonal Antibodies, in Participants With Advanced Solid Tumors |
| 2028-01-01 | US | IMTX | Immatics N.V. | Phase 3 | SUPRAME-ACTengine® IMA203 vs. Investigator's Choice of Treatment in Previously Treated, Unresectable or Metastatic Cutaneous Melanoma |
| 2028-01-01 | Ex-US | JBPHF | Jacobio Pharmaceuticals Group Co., Ltd. | Phase 2 | A First-in-Human, JAB-8263 in Adult Patients With Advanced Tumors |
| 2028-01-01 | US | KPTI | Karyopharm Therapeutics Inc. | Phase 2 | A Study of Selinexor (Seli) + Low-dose Dexamethasone (LDD) in Penta-refractory Multiple Myeloma (MM), Seli and Bortezomib + LDD in Triple-class Refractory MM. |
| 2028-01-01 | US | LXRX | Lexicon Pharmaceuticals, Inc. | Phase 2 | Combination Adjunctive Therapy to Address Multiple Metabolic Imbalances in Type 1 Diabetes |
| 2028-01-01 | US | NRIX | Nurix Therapeutics, Inc. | Phase 2 | A Study of NX-5948 in Adults With CLL/SLL Previously Treated With a Bruton's Tyrosine Kinase Inhibitor and a B-cell Lymphoma-2 Inhibitor (DAYBreak CLL-201) |
| 2028-01-01 | US | OGN | Organon & Co. | Phase 3 | A Study to Investigate Safety and Efficacy of Tapinarof Cream, 1% in Participants Ages 3 Months to < 24 Months With Atopic Dermatitis |
| 2028-01-01 | US | OPK | OPKO Health, Inc. | Phase 2 | Dose Escalation and Dose Expansion Study of MDX2003 in Patients With Different Types of Lymphoma |
| 2028-01-01 | US | RXRX | Recursion Pharmaceuticals, Inc. | Phase 2 | Study to Assess GTAEXS617 in Participants With Advanced Solid Tumors |
| 2028-01-01 | US | SRNE | Sorrento Therapeutics, Inc. | Phase 2 – Suspended | Study to Assess Abivertinib in Combination With Abiraterone in Metastatic Castration Resistant Prostate Cancer |
| 2028-01-01 | US | TYRA | Tyra Biosciences, Inc. | Phase 1 | Safety and Preliminary Anti-Tumor Activity of TYRA-430 in Advanced Hepatocellular Carcinoma and Other Solid Tumors With Activating FGF/FGFR Pathway Aberrations |
| 2028-01-15 | US | VSTM | Verastem, Inc. | Phase 2 | Defactinib and Avutometinib, With or Without Encorafenib, for the Treatment of Patients With Brain Metastases From Cutaneous Melanoma |
| 2028-01-17 | US | AGIO | Agios Pharmaceuticals, Inc. | Phase 1 | A Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of AG-181 in Subjects With Phenylketonuria |
| 2028-01-30 | US | MNKD | MannKind Corporation | Phase 2 | Phase 2 Clinical Trial of MNKD-201 (Nintedanib Dry Powder Inhalation) in Patients With Idiopathic Pulmonary Fibrosis |
| 2028-01-31 | US | ANL | Adlai Nortye Ltd. | Phase 1 | Evaluation of RAS Inhibitor Treatment in Participants With Advanced or Metastatic Solid Tumors Harboring RAS Mutations |
| 2028-02-01 | US | ACAD | ACADIA Pharmaceuticals Inc. | Phase 2 | Phase 2, Efficacy and Safety Study of ACP-204 in Lewy Body Dementia Psychosis |
| 2028-02-01 | US | AGEN | Agenus Inc. | Phase 2 | A Study of Botensilimab (AGEN1181) for the Treatment of Advanced Melanoma |
| 2028-02-01 | US | BEAM | Beam Therapeutics Inc. | Phase 2 | BEACON: A Study Evaluating the Safety and Efficacy of BEAM-101 in Patients With Severe Sickle Cell Disease |
| 2028-02-01 | US | BHVN | Biohaven Ltd. | Phase 2 | A Phase 1/2 Study of BHV-1510 (Previously PBI-410) in Advanced Solid Tumors |
| 2028-02-01 | US | CLRB | Cellectar Biosciences, Inc. | Phase 1 | Phase 1 Study of CLR 125 in Triple Negative Breast Cancer |
| 2028-02-01 | US | NXTC | NextCure, Inc. | Phase 1 | A Phase I Study of SIM0505 in Participants With Advanced Solid Tumors |
| 2028-02-01 | US | TYRA | Tyra Biosciences, Inc. | Phase 2 | Efficacy and Safety of TYRA-300 in Participants With FGFR3 Altered Low Grade, Intermediate Risk Non-Muscle Invasive Bladder Cancer |
| 2028-02-03 | US | RAPP | Rapport Therapeutics, Inc. | Phase 2 | A Long-term Study of the Safety and Effectiveness of RAP-219 in Adults With Focal Onset Seizures |
| 2028-02-04 | US | MLTX | MoonLake Immunotherapeutics | Phase 3 | A Study to Evaluate the Long-term Safety, Tolerability, and Efficacy of Subcutaneous Sonelokimab in Participants With Psoriatic Arthritis |
| 2028-02-28 | Ex-US | JCRRF | JCR Pharmaceuticals Co., Ltd. | Phase 3 | An Extension Study of JR-141 to Evaluate the Long-term Safety and Efficacy in MPS II (Hunter Syndrome) Subjects |
| 2028-02-28 | US | MRKR | Marker Therapeutics, Inc. | Phase 1 | Safety and Preliminary Efficacy of MT-601 in Patients With Relapsed/Refractory Lymphoma |
| 2028-03-01 | US | ARVN | Arvinas, Inc. | Phase 1 | A Study of ARV-393 in Relapsed/Refractory Non-Hodgkin Lymphoma. |
| 2028-03-01 | US | GNPX | Genprex, Inc. | Phase 2 | Quaratusugene Ozeplasmid (Reqorsa) and Osimertinib in Patients With Advanced Lung Cancer Who Progressed on Osimertinib |
| 2028-03-01 | US | IOVA | Iovance Biotherapeutics, Inc. | Phase 3 | Study to Investigate Lifileucel Regimen Plus Pembrolizumab Compared With Pembrolizumab Alone in Participants With Untreated Advanced Melanoma. |
| 2028-03-01 | Ex-US | NPPNY | Nippon Shinyaku Co., Ltd. | Phase 2 | NS-050/NCNP-03 in Boys With DMD (Meteor50) |
| 2028-03-15 | US | CGEM | Cullinan Therapeutics, Inc. | Phase 1 | A Study of CLN-978, a Subcutaneously Administered CD19-directed T Cell Engager, in Subjects With Sjogren's Disease |
| 2028-03-21 | US | SLDB | Solid Biosciences Inc. | Phase 1 | A Study of SGT-212 Gene Therapy in Friedreich's Ataxia |
| 2028-03-26 | US | KPTI | Karyopharm Therapeutics Inc. | Phase 2 | Selinexor, Venetoclax, and Dexamethasone (XVenD) in t(11;14)-Positive Relapsed/Refractory Multiple Myeloma |
| 2028-03-31 | US | GERN | Geron Corporation | Phase 1 | A Study to Find the Highest Dose of Imetelstat in Combination With Fludarabine and Cytarabine for Patients With AML, MDS or JMML That Has Come Back or Does Not Respond to Therapy |
| 2028-03-31 | US | PBYI | Puma Biotechnology, Inc. | Phase 2 | A Study of Alisertib and Paclitaxel in Patients With Small Cell Lung Cancer (SCLC) |
| 2028-03-31 | US | REPL | Replimune Group, Inc. | Phase 1 | RP1 in Primary Melanoma to Reduce the Risk of Sentinel Lymph Node Metastasis |
| 2028-04-01 | US | ARQT | Arcutis Biotherapeutics, Inc. | Phase 1 | Ph 1a/1b Single Ascending Dose and Multiple Ascending Dose Study of ARQ-234 |
| 2028-04-01 | Ex-US | IDRSF | Idorsia Ltd | Phase 2 – Suspended | Department of Defense PTSD Adaptive Platform Trial – Intervention C – Daridorexant |
| 2028-04-01 | US | RCKT | Rocket Pharmaceuticals, Inc. | Phase 2 | A Gene Therapy Study of RP-A501 in Male Patients With Danon Disease |
| 2028-04-01 | US | RCUS | Arcus Biosciences, Inc. | Phase 3 | Study of Casdatifan and Cabozantinib Versus Placebo and Cabozantinib in Patients With Advanced Clear Cell Renal Cell Carcinoma |
| 2028-04-01 | US | UPB | Upstream Bio, Inc. | Phase 2 | A Study to Assess the Efficacy and Safety of Verekitug in Participants With COPD |
| 2028-04-01 | US | XNCR | Xencor, Inc. | Phase 2 | Study of XmAb942 in Healthy Participants and Participants With Ulcerative Colitis |
| 2028-04-20 | US | CLDX | Celldex Therapeutics, Inc. | Phase 1 | CD40 Agonist, Flt3 Ligand, and Chemotherapy in HER2 Negative Breast Cancer |
| 2028-04-30 | US | IPHA | Innate Pharma S.A. | Phase 2 | Study of Lacutamab in Peripheral T-cell Lymphoma |
| 2028-04-30 | US | RGNX | REGENXBIO Inc. | Phase 3 | RGX-121-3102 Gene Therapy in Participants With MPS II (Hunter Syndrome) |
| 2028-04-30 | US | RLAY | Relay Therapeutics, Inc. | Phase 3 | Phase 3 Study of RLY-2608 + Fulvestrant vs Capivasertib + Fulvestrant as Treatment for Locally Advanced or Metastatic PIK3CA-mutant HR+/HER2- Breast Cancer |
| 2028-04-30 | US | VRCA | Verrica Pharmaceuticals Inc. | Phase 3 | Long-Term Follow-up Study of Cantharidin (YCANTH [VP-102/TO-208]) in Patients With Common Warts (Verruca Vulgaris) |
| 2028-05-01 | US | BEAM | Beam Therapeutics Inc. | Phase 2 | A Study to Evaluate the Safety and Efficacy of BEAM-302 in Adult Patients With Alpha-1 Antitrypsin Deficiency (AATD) |
| 2028-05-01 | Ex-US | IDRSF | Idorsia Ltd | Phase 2 – Suspended | Department of Defense PTSD Adaptive Platform Trial – Intervention A – Fluoxetine |
| 2028-05-01 | Ex-US | IDRSF | Idorsia Ltd | Phase 2 | Department of Defense PTSD Adaptive Platform Trial – Intervention B – Vilazodone |
| 2028-05-01 | US | IOVA | Iovance Biotherapeutics, Inc. | Phase 2 | A Study of Lifileucel (Tumor-infiltrating Lymphocytes) in Adults With Advanced Endometrial Cancer. |
| 2028-05-30 | US | CHRS | Coherus Oncology, Inc. | Phase 1 | A Study of CHS-1000 in Participants With Advanced or Metastatic Solid Tumors |
| 2028-05-31 | US | CNTX | Context Therapeutics Inc. | Phase 1 | A Phase 1 Study of CTIM-76 in Patients With Recurring Ovarian Cancer and Other Advanced Solid Tumors |
| 2028-05-31 | US | ZNTL | Zentalis Pharmaceuticals, Inc. | Phase 3 | A Study of Azenosertib (ZN-c3) Versus Investigator's Choice Chemotherapy in Subjects With Platinum-Resistant High-Grade Serous Ovarian, Primary Peritoneal, or Fallopian Tube Cancers Positive for Cyclin E1 Protein Expression |
| 2028-06-01 | US | IMRX | Immuneering Corporation | Phase 3 | Atebimetinib + GnP as a First Line Treatment in Patients With Metastatic Pancreatic Adenocarcinoma |
| 2028-06-01 | US | IRON | Disc Medicine, Inc. | Phase 3 | HELIOS: Open-Label, Long-Term Extension Study to Investigate the Safety, Tolerability, and Efficacy of DISC-1459 (Bitopertin) in Participants With EPP or XLP |
| 2028-06-01 | Ex-US | LYPHF | Luye Pharma Group Ltd. | Phase 3 | Study of LY01610 in Patients With Recurrent Small Cell Lung Cancer |
| 2028-06-01 | US | RXRX | Recursion Pharmaceuticals, Inc. | Phase 1 | Dose Determining Study of EXS73565 in Participants With Relapsed or Refractory B-Cell Malignancies |
| 2028-06-01 | US | XENE | Xenon Pharmaceuticals Inc. | Phase 3 | A Randomized Study of Azetukalner Versus Placebo in Depressive Episodes Associated With Bipolar I or II Disorder (Bipolar Depression) |
| 2028-06-01 | US | XNCR | Xencor, Inc. | Phase 1 | A Phase 1b Open-label Study to Evaluate Safety of Plamotamab in Participants With Rheumatoid Arthritis |
| 2028-06-13 | US | MLTX | MoonLake Immunotherapeutics | Phase 3 | A Study to Evaluate the Long-term Safety, Tolerability, and Efficacy of Subcutaneous Sonelokimab in Participants With Moderate to Severe Hidradenitis Suppurativa |
| 2028-06-30 | US | GERN | Geron Corporation | Phase 3 | A Study Comparing Imetelstat Versus Best Available Therapy for the Treatment of Intermediate-2 or High-risk Myelofibrosis (MF) Who Have Not Responded to Janus Kinase (JAK)-Inhibitor Treatment |
| 2028-06-30 | Ex-US | JCRRF | JCR Pharmaceuticals Co., Ltd. | Phase 2 | A Phase I/II Trial of JR-446 in Mucopolysaccharidosis Type IIIB (MPS IIIB) |
| 2028-06-30 | US | MGNX | MacroGenics, Inc. | Phase 2 – Suspended | Triage of Advanced Cervical Cancer Through Immunotherapy Induction (TRACTION) |
| 2028-06-30 | US | TENX | Tenax Therapeutics, Inc. | Phase 3 | LEVEL-2: LEVosimendan to Improve Exercise Limitation in Patients With PH-HFpEF-2 |
| 2028-06-30 | US | ZNTL | Zentalis Pharmaceuticals, Inc. | Phase 1 | A Study of Azenosertib (ZN-c3) in Patients With Ovarian Cancer |
| 2028-07-01 | Ex-US | IDRSF | Idorsia Ltd | Phase 2 – Suspended | Department of Defense PTSD Adaptive Platform Trial – Master Protocol |
| 2028-07-01 | US | TGTX | TG Therapeutics, Inc. | Phase 2 | A Study to Evaluate the Efficacy and Safety of Maintenance Ublituximab Following Induction With Efgartigimod Administration in Participants With Myasthenia Gravis (MG) |
| 2028-07-09 | US | FTRE | Fortrea Holdings Inc. | Phase 3 | Pediatric Patients Aged 1 to 6 Years With APDS |
| 2028-07-09 | US | PHAR | Pharming Group N.V. | Phase 3 | Pediatric Patients Aged 1 to 6 Years With APDS |
| 2028-07-09 | US | PHAR | Pharming Group N.V. | Phase 3 | Pediatric Patients Aged 1 to 6 Years With APDS |
| 2028-07-16 | US | MRKR | Marker Therapeutics, Inc. | Phase 1 | MT-601 Administered To Patients With Locally Advanced Unresectable or Metastatic Pancreatic Cancer |
| 2028-07-31 | US | CRIS | Curis, Inc. | Phase 1 | CA-4948 in Combination With FOLFOX/PD-1 Inhibitor +/- Trastuzumab for Untreated Unresectable Gastric and Esophageal Cancer |
| 2028-08-01 | US | DNLI | Denali Therapeutics Inc. | Phase 1 | A Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of DNL952 in Adult Participants With Late-Onset Pompe Disease |
| 2028-08-01 | US | DNLI | Denali Therapeutics Inc. | Phase 2 | Study of DNL126 in Pediatric Participants With Mucopolysaccharidosis Type IIIA (Sanfilippo Syndrome Type A) |
| 2028-08-01 | US | HOWL | Werewolf Therapeutics, Inc. | Phase 2 | A Phase 1b/2 Multisite Dose-finding and Expansion Study of WTX-330 in Adult Patients With Selected Advanced or Metastatic Solid Tumors or Lymphoma |
| 2028-08-28 | US | SRPT | Sarepta Therapeutics, Inc. | Phase 1 | A Gene Transfer Single Dose Study to Evaluate the Safety, Tolerability and Efficacy of SRP-9003 in Non-Ambulatory and Ambulatory Participants With Limb Girdle Muscular Dystrophy, Type 2E/R4 (Beta-Sarcoglycan [β-SG] Deficiency) |
| 2028-09-01 | US | BHVN | Biohaven Ltd. | Phase 3 | A Study to Determine if BHV-1400 is Effective and Safe in Adults With IgA Nephropathy |
| 2028-09-01 | US | MOLN | Molecular Partners AG | Phase 2 | Study of [212Pb]Pb-DOTAM-MAM279 ([212Pb]Pb-MP0712) in Patients With Small Cell Lung Cancer and Other DLL3 Expressing Solid Tumors |
| 2028-09-01 | US | RCKT | Rocket Pharmaceuticals, Inc. | Phase 1 | A Phase 1, Dose Escalation Trial of RP-A601 in Subjects With PKP2 Variant-Mediated Arrhythmogenic Cardiomyopathy (PKP2-ACM) |
| 2028-09-01 | US | XBIT | XBiotech Inc. | Phase 2 | Vilamakitug in Spondyloarthritis Placebo-controlled Investigation for Efficacy |
| 2028-09-15 | US | BCAB | BioAtla, Inc. | Phase 1 | Phase 1 Study Evaluating BA3182 in Patients With Advanced Adenocarcinoma. |
| 2028-10-01 | US | NKTX | Nkarta, Inc. | Phase 2 | A Phase 1/2 Study of NKX019 in Subjects With Immune-Mediated Diseases (Ntrust-2) |
| 2028-10-01 | US | XNCR | Xencor, Inc. | Phase 1 | A Phase 1 Open-label Study to Evaluate Safety in Healthy Participants and Participants With Autoimmune Diseases |
| 2028-10-15 | US | VSTM | Verastem, Inc. | Phase 3 | A Study of Avutometinib (VS-6766) + Defactinib (VS-6063) in Recurrent Low-Grade Serous Ovarian Cancer |
| 2028-10-16 | US | KURA | Kura Oncology, Inc. | Phase 2 | First in Human Study of Ziftomenib in Relapsed or Refractory Acute Myeloid Leukemia |
| 2028-10-29 | Ex-US | NURPF | Neuren Pharmaceuticals Limited | Phase 3 | An Open-label Study of NNZ-2591 in Pediatric Participants With Phelan-McDermid Syndrome |
| 2028-10-30 | US | RXRX | Recursion Pharmaceuticals, Inc. | Phase 2 | A Study of REC-1245 in Participants With Unresectable, Locally Advanced, or Metastatic Cancer |
| 2028-10-31 | US | RIGL | Rigel Pharmaceuticals, Inc. | Phase 1 | Olutasidenib Single Plus Combo Therapy in IDH1mut AML After Induction and Consolidation |
| 2028-11-01 | US | ALMS | Alumis Inc. | Phase 3 | Long-term Safety and Efficacy of ESK-001 in Moderate to Severe Plaque Psoriasis |
| 2028-11-01 | US | BBOT | BridgeBio Oncology Therapeutics, Inc. | Phase 1 | Open-Label Study of BBO-10203 in Subjects With Advanced Solid Tumors |
| 2028-11-02 | US | TSHA | Taysha Gene Therapies, Inc. | Phase 2 | Safety and Efficacy of TSHA-102 in Pediatric Females With Rett Syndrome (REVEAL Pediatric Study) |
| 2028-11-30 | Ex-US | ALMRY | Almirall SA | Phase 3 | Efficacy and Safety of Cryotherapy Followed by Tirbanibulin Ointment for Actinic Keratosis on the Scalp and Forehead |
| 2028-11-30 | Ex-US | LBTSF | Almirall, S.A. | Phase 3 | Efficacy and Safety of Cryotherapy Followed by Tirbanibulin Ointment for Actinic Keratosis on the Scalp and Forehead |
| 2028-12-01 | US | APLS | Apellis Pharmaceuticals, Inc. | Phase 2 | A Study of Pegcetacoplan in Pediatric Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH) |
| 2028-12-01 | US | INBX | Inhibrx Biosciences, Inc. | Phase 1 | Phase 1 Study of INBRX-109 in Subjects With Locally Advanced or Metastatic Solid Tumors Including Sarcomas |
| 2028-12-01 | US | MYGN | Myriad Genetics, Inc. | Phase 1 | SHARON: A Clinical Trial for Metastatic Cancer Using Chemotherapy and Patients' Own Stem Cells |
| 2028-12-01 | US | NUVB | Nuvation Bio Inc. | Phase 3 | SIGMA (Safusidenib in IDH1 Mutant Glioma Maintenance) |
| 2028-12-01 | US | OLMA | Olema Pharmaceuticals, Inc. | Phase 3 | Palazestrant in Combination With Ribociclib for the First-line Treatment of ER+/HER2- Advanced Breast Cancer |
| 2028-12-01 | US | OTLC | Oncotelic Therapeutics, Inc. | Phase 2 | OT-101 in Combination With Pembrolizumab in Subjects With Malignant Pleural Mesothelioma Failing to Respond to Checkpoint Inhibition |
| 2028-12-01 | US | VSTM | Verastem, Inc. | Phase 2 | A Phase 1/2 Study of VS-7375 in Patients With KRAS G12D-Mutated Solid Tumors |
| 2028-12-01 | US | XNCR | Xencor, Inc. | Phase 1 | Phase 1, Safety and Tolerability Study of XmAb541 and XmAb808 in Advanced Solid Tumors |
| 2028-12-31 | Ex-US | LYPHF | Luye Pharma Group Ltd. | Phase 2 | LPM6690176 in Combination With Chemotherapy and Bevacizumab in Metastatic Colorectal Cancer Patients With RAS Mutation |
| 2028-12-31 | US | RARE | Ultragenyx Pharmaceutical Inc. | Phase 1 | Triheptanoin for Children With Primary-Specific Pyruvate Dehydrogenase Complex (PDC) Deficiency |
| 2028-12-31 | US | VCNX | Vaccinex, Inc. | Phase 2 | Trial of Immunotherapy With Avelumab and Pepinemab As Second Line For Patients With Metastatic Pancreatic Adenocarcinoma |
| 2029-01-01 | US | JBIO | Jade Biosciences, Inc. | Phase 2 | A Study of JADE101 in Participants With Immunoglobulin A Nephropathy |
| 2029-01-01 | US | MIST | Milestone Pharmaceuticals Inc. | Phase 3 | ReVeRA-301: Etripamil in Atrial Fibrillation Phase 3 |
| 2029-01-01 | US | NUVB | Nuvation Bio Inc. | Phase 3 | A Phase III Study Comparing Taletrectinib With Standard Therapy in ROS1 Positive Locally Advanced or Metastatic Non-small Cell Lung Cancer Patients |
| 2029-01-01 | US | PEPG | PepGen Inc. | Phase 2 | An Open-Label Extension Study of PGN-EDODM1 in People With Myotonic Dystrophy Type 1 (FREEDOM-OLE) |
| 2029-01-01 | US | RCKT | Rocket Pharmaceuticals, Inc. | Phase 2 – Suspended | Clinical Trial to Evaluate the Efficacy of Gene Therapy for Pyruvate Kinase Deficiency |
| 2029-01-01 | US | RCKT | Rocket Pharmaceuticals, Inc. | Phase 2 – Suspended | Clinical Trial to Evaluate the Efficacy of Gene Therapy for Pyruvate Kinase Deficiency |
| 2029-01-01 | US | SLDB | Solid Biosciences Inc. | Phase 3 | A Study of SGT-003 Gene Therapy in Ambulant Males With Duchenne Muscular Dystrophy (IMPACT DUCHENNE) |
| 2029-02-01 | US | ACAD | ACADIA Pharmaceuticals Inc. | Phase 3 | Phase 3, Open Label Extension Study of ACP-204 in Lewy Body Dementia Psychosis |
| 2029-02-01 | Ex-US | CASBF | CanSino Biologics Inc. | Phase 1 | Clinical Trial of the Adsorbed Acellular Pertussis (Tricomponent) DTaP-Haemophilus Influenzae Type b (Conjugate)-ACYW135 Group Meningococcal (Conjugate) Combined Vaccine |
| 2029-02-28 | US | BOLD | Boundless Bio, Inc. | Phase 1 | Study of the Kinesin Oral Molecular Degrader BBI-940 in Subjects With Advanced or Metastatic Breast Cancer |
| 2029-03-01 | US | ABEO | Abeona Therapeutics Inc. | Phase 3 | Phase I/II/III Gene Transfer Clinical Trial of scAAV9.U1a.hSGSH |
| 2029-03-01 | US | AGIO | Agios Pharmaceuticals, Inc. | Phase 3 | A Study to Investigate the Efficacy, Pharmacokinetics, and Safety of Mitapivat in Pediatric Participants With α- or β-Non-Transfusion-Dependent Thalassemia |
| 2029-03-01 | US | BHVN | Biohaven Ltd. | Phase 1 | A Phase 1 Study of BHV-1530 in Advanced Solid Tumors |
| 2029-03-01 | US | RARE | Ultragenyx Pharmaceutical Inc. | Phase 3 | Phase I/II/III Gene Transfer Clinical Trial of scAAV9.U1a.hSGSH |
| 2029-03-01 | US | RARE | Ultragenyx Pharmaceutical Inc. | Phase 2 | A Phase 1/2/3 Study of UX701 Gene Therapy in Adults With Wilson Disease |
| 2029-03-01 | US | RCUS | Arcus Biosciences, Inc. | Phase 1 | A Phase 1 Study of AB521 Monotherapy and Combination Therapies in Renal Cell Carcinoma and Other Solid Tumors |
| 2029-03-01 | US | RXRX | Recursion Pharmaceuticals, Inc. | Phase 1 | Dose Determining Study of EXS74539 (REC-4539) in Participants With Select Solid Tumors |
| 2029-03-01 | US | TENX | Tenax Therapeutics, Inc. | Phase 3 | Long-Term Open-Label Extension Study of Oral Levosimendan |
| 2029-03-02 | US | AUPH | Aurinia Pharmaceuticals Inc. | Phase 2 | Study of Aritinercept in Patients With Generalized Myasthenia Gravis |
| 2029-03-02 | US | SYRE | Spyre Therapeutics, Inc. | Phase 2 | Long-term Safety and Efficacy of Multiple Long-acting Antibodies Alone and in Combinations for IBD |
| 2029-03-31 | US | CELC | Celcuity Inc. | Phase 3 | Phase 3 Study of Gedatolisib as First-Line Treatment for Patients With HR-Positive, HER2-Negative Advanced Breast Cancer (VIKTORIA-2) |
| 2029-03-31 | US | STOK | Stoke Therapeutics, Inc. | Phase 2 | An Open-Label Extension Study of STK-001 for Patients With Dravet Syndrome |
| 2029-04-01 | US | ACAD | ACADIA Pharmaceuticals Inc. | Phase 3 | ACP-204 in Adults With Alzheimer's Disease Psychosis Open Label Extension Study |
| 2029-04-01 | US | ACIU | AC Immune SA | Phase 2 | A Study to Assess the Effects of ACI-24.060 in Alzheimer's Disease and in Down Syndrome (ABATE Study) |
| 2029-05-01 | US | ACAD | ACADIA Pharmaceuticals Inc. | Phase 3 | OLE Study of Carbetocin Nasal Spray for the Treatment of Hyperphagia in Prader-Willi Syndrome |
| 2029-05-01 | US | DCTH | Delcath Systems, Inc. | Phase 2 | Evaluation of the Safety and Efficacy of Treatment w/High Dose Melphalan Given Directly Into the Liver Followed by Treatment w/Approved Cancer Treatment or Approved Cancer Treatment Alone in Patients w/ Metastatic Breast Cancer w/Liver Dominant Disease |
| 2029-05-01 | Ex-US | IDRSF | Idorsia Ltd | Phase 2 – Suspended | Department of Defense PTSD Adaptive Platform Trial – Intervention D – SLS-002 |
| 2029-05-01 | US | INBX | Inhibrx Biosciences, Inc. | Phase 3 | INBRX-106 in Combination With Pembrolizumab in First-line PD-L1 CPS≥20 HNSCC |
| 2029-05-01 | US | MIRM | Mirum Pharmaceuticals, Inc. | Phase 3 | A Trial Evaluating BJT-778 vs Delayed Treatment for the Treatment of Chronic Hepatitis Delta Infection |
| 2029-06-01 | US | APLS | Apellis Pharmaceuticals, Inc. | Phase 3 – Suspended | Study to Evaluate the Efficacy and Safety of Pegcetacoplan in Adults at High Risk of Delayed Graft Function (DGF) Following Kidney Allograft Transplantation |
| 2029-06-01 | US | BYSI | BeyondSpring Inc. | Phase 3 | Docetaxel Plus Plinabulin vs Docetaxel Plus Placebo in Advanced/Metastatic Non-Squamous NSCLC After PD-1/PD-L1 Therapy and Platinum Chemotherapy (DUBLIN-4) |
| 2029-06-01 | US | RCKT | Rocket Pharmaceuticals, Inc. | Phase 1 | A Phase 1 AAV Gene Therapy Trial Evaluating Safety and Preliminary Efficacy of RP-A701 in Subjects With BAG3 Dilated Cardiomyopathy |
| 2029-06-01 | US | XENE | Xenon Pharmaceuticals Inc. | Phase 3 | An Open-label Study of Azetukalner in Bipolar I or II Depression (X-CEED-OLE) |
| 2029-06-30 | US | TVRD | Tvardi Therapeutics, Inc. | Phase 1 | Radiotherapy in Combination With TTI-101 in Borderline Resectable and Locally Advanced Pancreatic Ductal Adenocarcinoma |
| 2029-07-01 | Ex-US | INNMF | Amplia Therapeutics Limited | Phase 2 | A Study of Narmafotinib Given in Combination With Modified FOLFIRINOX in Patients With Metastatic Pancreatic Cancer |
| 2029-07-01 | US | RAPP | Rapport Therapeutics, Inc. | Phase 3 | Study Evaluating the Efficacy and Safety of RAP-219 in Adult Participants With Focal Seizures FOCUS-1 |
| 2029-07-01 | US | RAPP | Rapport Therapeutics, Inc. | Phase 3 | Study Evaluating the Efficacy and Safety of RAP-219 in Adult Participants With Focal Seizures |
| 2029-07-01 | US | REPL | Replimune Group, Inc. | Phase 2 | Study to Investigate the Efficacy and Safety of RP1 in Adult Patients With Organ Transplants and Advanced Skin Malignancies |
| 2029-08-01 | US | AGIO | Agios Pharmaceuticals, Inc. | Phase 3 | A Study to Investigate the Effect of Mitapivat on Transfusion Burden in Subjects With Sickle Cell Disease (SCD) |
| 2029-08-01 | Ex-US | IDRSF | Idorsia Ltd | Phase 3 | A Study to Evaluate the Long-term Safety and Tolerability of Lucerastat in Adult Subjects With Fabry Disease |
| 2029-08-01 | US | MBRX | Moleculin Biotech, Inc. | Phase 3 | L-Annamycin for Injection in Combination With Cytarabine Injection as Second Line Therapy for Remission Induction in Adult Subjects With Refractory/Relapsed AML |
| 2029-08-01 | US | VIR | Vir Biotechnology, Inc. | Phase 1 | Safety and Preliminary Efficacy of VIR-5525 and VIR-5525 + Pembrolizumab in Participants With Locally Advanced or Metastatic Solid Tumors |
| 2029-09-01 | US | ANVS | Annovis Bio, Inc. | Phase 3 | A Study of Buntanetap in Participants With PD |
| 2029-09-01 | US | MRKR | Marker Therapeutics, Inc. | Phase 1 | Safety of MT-401-OTS in Patients With Relapsed AML or MDS |
| 2029-09-01 | US | RLMD | Relmada Therapeutics, Inc. | Phase 3 | A Study of NDV-01 (Sustained-release Gemcitabine-docetaxel) in Participants With Non-muscle Invasive Bladder Cancer |
| 2029-10-01 | US | NRIX | Nurix Therapeutics, Inc. | Phase 3 | Study of NX-5948 Versus Pirtobrutinib in R/R CLL/SLL |
| 2029-10-01 | Ex-US | PYCXF | PYC THERAPEUTICS LTD. | Phase 2 | Safety of Single and Repeat Dose of PYC-001 Eye Injections in People With Autosomal Dominant Optic Atrophy (Myrtle) |
| 2029-10-31 | Ex-US | JCRRF | JCR Pharmaceuticals Co., Ltd. | Phase 2 | Phase I/II Study of JR-441 in Patients With Mucopolysaccharidosis Type IIIA |
| 2029-12-01 | Ex-US | CSPHF | CStone Pharmaceuticals | Phase 3 | Study of Sugemalimab (or Placebo) Plus PGemOx Regimen in Participants With Extranodal NK/T-Cell Lymphoma |
| 2029-12-01 | Ex-US | ORPOF | OSE IMMUNOTHERAPEUTICS | Phase 2 | Dose-finding and Dose Expansion Study of OSE-279 in Subjects With Advanced Solid Tumors or Lymphomas |
| 2029-12-01 | US | PROK | ProKidney Corp. | Phase 3 | Proact: A Study of REACT in Subjects With Type 2 Diabetes Mellitus and Chronic Kidney Disease |
| 2029-12-31 | US | PBYI | Puma Biotechnology, Inc. | Phase 2 – Suspended | Neratinib + Valproate in Advanced Solid Tumors, w/Expansion Cohort in Ras-Mutated Ca |
| 2030-01-01 | US | CNTX | Context Therapeutics Inc. | Phase 1 | A Phase 1a/1b, First-Time-in-Human Study of CT-202, a Nectin-4 Directed Bispecific Antibody, in Participants With Recurring Triple Negative Breast, Colorectal, Urothelial Cancers |
| 2030-01-01 | US | RARE | Ultragenyx Pharmaceutical Inc. | Phase 2 | A Safety and Efficacy Study of GTX-102 in Subjects With Deletion- or Nondeletion-type Angelman Syndrome (AS) |
| 2030-01-01 | US | TGTX | TG Therapeutics, Inc. | Phase 3 | Study to Assess Effects of Ublituximab in Pediatric Participants With Relapsing Forms of Multiple Sclerosis |
| 2030-01-01 | US | TYRA | Tyra Biosciences, Inc. | Phase 2 | A Study of TYRA-300 in Children With Achondroplasia: BEACH301 |
| 2030-02-01 | US | VCEL | Vericel Corporation | Phase 3 | A Study of MACI in Patients Aged 10 to 17 Years With Symptomatic Chondral or Osteochondral Defects of the Knee |
| 2030-03-31 | Ex-US | JCRRF | JCR Pharmaceuticals Co., Ltd. | Phase 3 | An Extension Study of JR-141 in Patients With Mucopolysaccharidosis Type II |
| 2030-04-01 | US | KURA | Kura Oncology, Inc. | Phase 1 | A Study to Investigate the Safety and Tolerability of Ziftomenib in Combination With Venetoclax/Azacitidine, Venetoclax, 7+3, or 7+3+Quizartinib in Patients With AML |
| 2030-04-30 | Ex-US | JCRRF | JCR Pharmaceuticals Co., Ltd. | Phase 2 | An Open-label Phase I/II Study of JR-446 in Mucopolysaccharidosis Type IIIB |
| 2030-05-01 | US | CASI | CASI Pharmaceuticals, Inc. | Phase 2 | A Two Part Dose-escalation Safety and Efficacy Study of CID-103 in Adults With Active and Chronic Active Renal Allograft Antibody Mediated Rejection (ABMR). |
| 2030-05-01 | US | ORKA | Oruka Therapeutics, Inc. | Phase 2 | An Open-Label Extension Study of ORKA-001 in Participants With Plaque Psoriasis |
| 2030-06-16 | US | CGON | CG Oncology, Inc. | Phase 3 | Study of Cretostimogene Given in Patients With Non-Muscle Invasive Bladder Cancer ,Unresponsive to Bacillus-Calmette-Guerin |
| 2030-07-01 | US | VCEL | Vericel Corporation | Phase 3 | A Study of MACI in Patients Aged 17 to 65 Years With Symptomatic Chondral or Osteochondral Defects of the Ankle |
| 2030-08-01 | US | OCUL | Ocular Therapeutix, Inc. | Phase 3 | Study to Evaluate Long-Term Safety of Intravitreal OTX-TKI (Axitinib Implant) in Participants With Neovascular Age-Related Macular Degeneration Who Successfully Completed 2-Year OTX-TKI-2023-AMD-301 or OTX-TKI-2023-AMD-303 Study |
| 2030-08-01 | US | TVTX | Travere Therapeutics, Inc. | Phase 3 | A Long-term Extension Study to Assess the Long-term Safety and Efficacy of Pegtibatinase Treatment in Participants ≥5 to ≤65 Years of Age With Classical Homocystinuria (HCU) (ENSEMBLE) |
| 2030-08-01 | US | TVTX | Travere Therapeutics, Inc. | Phase 3 | A Long-term Extension Study to Assess the Long-term Safety and Efficacy of Pegtibatinase Treatment in Participants ≥5 to ≤65 Years of Age With Classical Homocystinuria (HCU) (ENSEMBLE) |
| 2030-08-30 | US | NUVB | Nuvation Bio Inc. | Phase 3 | Phase 3 Study of Taletrectinib vs Placebo as an Adjuvant Therapy in ROS1 Positive NSCLC (TRUST-IV) |
| 2030-09-01 | Ex-US | KSPHF | Kissei Pharmaceutical Co., Ltd. | Phase 2 | A Clinical Trial of Olutasidenib in Patients With Acute Myeloid Leukemia |
| 2030-10-01 | US | TYRA | Tyra Biosciences, Inc. | Phase 2 | Phase 2A/B Efficacy and Safety of Dabogratinib in Participants With Low Grade Upper Tract Urothelial Carcinoma |
| 2030-11-30 | US | RCUS | Arcus Biosciences, Inc. | Phase 3 | Study of Quemliclustat and Chemotherapy Versus Placebo and Chemotherapy in Patients With Metastatic Pancreatic Ductal Adenocarcinoma |
| 2030-12-01 | US | IOVA | Iovance Biotherapeutics, Inc. | Phase 2 | Autologous LN-145 in Patients With Metastatic Non-Small-Cell Lung Cancer |
| 2031-02-01 | US | DNLI | Denali Therapeutics Inc. | Phase 2 | A Study of Tividenofusp Alfa (DNL310) in Pediatric Participants With Hunter Syndrome |
| 2031-02-01 | US | EWTX | Edgewise Therapeutics, Inc. | Phase 2 | Open-Label Extension of EDG-5506 in Participants With Becker Muscular Dystrophy |
| 2031-03-01 | US | ATXS | Astria Therapeutics, Inc. | Phase 2 | A Long-term Study of STAR-0215 in Participants With Hereditary Angioedema |
| 2031-04-01 | US | BBOT | BridgeBio Oncology Therapeutics, Inc. | Phase 1 | Open-label Study of BBO-8520 in Adult Subjects With KRASG12C Non-small Cell Lung Cancer |
| 2031-05-21 | US | VERA | Vera Therapeutics, Inc. | Phase 2 | A Rollover Study to Evaluate the Long-Term Safety and Efficacy of Atacicept |
| 2031-06-01 | US | ATXS | Astria Therapeutics, Inc. | Phase 3 | A Long-Term Study of Navenibart in Participants With Hereditary Angioedema |
| 2031-06-01 | US | TSHA | Taysha Gene Therapies, Inc. | Phase 3 | Safety and Preliminary Efficacy of TSHA-102 Gene Therapy in Pediatric Females Aged >2 to <4 Years With Rett Syndrome |
| 2031-06-01 | US | TSHA | Taysha Gene Therapies, Inc. | Phase 3 | A Phase 1/2/3 Study of TSHA-102 Gene Therapy in Females With Rett Syndrome (REVEAL Pivotal Study) |
| 2031-07-01 | US | RLAY | Relay Therapeutics, Inc. | Phase 2 | A Phase 2 Study of Mutant-selective PI3Kα Inhibitor, RLY-2608, in Adults and Children With PIK3CA Related Overgrowth Spectrum and Malformations Driven by PIK3CA Mutation (The ReInspire Study) |
| 2031-07-31 | US | AGEN | Agenus Inc. | Phase 2 | Phase 2a Immune Modulation With Ultrasound for Newly Diagnosed Glioblastoma |
| 2031-09-30 | Ex-US | ASPHF | Ascentage Pharma Group International | Phase 2 | Phase II Study of the Combination of Subcutaneous Blinatumomab and Olverembatinib in Patients With Philadelphia Chromosome (ph)-Positive and/or BCR::ABL1 Positive Acute Lymphoblastic Leukemia (ALL) |
| 2031-10-22 | US | CADL | Candel Therapeutics, Inc. | Phase 3 | Aglatimagene Besadenovec + Prodrug and Pembrolizumab vs Docetaxel for Stage IV Non-Squamous NSCLC Progressing on Pembrolizumab (AURORA) |
| 2031-11-01 | US | KURA | Kura Oncology, Inc. | Phase 3 | Studies to Assess Ziftomenib in Combination With Ven+Aza or 7+3 in Patients With Untreated NPM1-m or KMT2A-r AML |
| 2031-11-01 | US | VIR | Vir Biotechnology, Inc. | Phase 2 | SOLSTICE: Combination Therapy for the Treatment of Chronic Hepatitis D Infection. |
| 2032-05-31 | US | TGTX | TG Therapeutics, Inc. | Phase 3 | An Extension Study of Ublituximab in Participants With Relapsing Multiple Sclerosis |
| 2032-06-01 | US | IOVA | Iovance Biotherapeutics, Inc. | Phase 2 | A Study to Investigate the Safety and Efficacy of IOV-3001 in Adults With Advanced Melanoma Who Will Receive Lifileucel |
| 2032-12-01 | US | IOVA | Iovance Biotherapeutics, Inc. | Phase 2 | A Study of Lifileucel (Tumor-infiltrating Lymphocytes) in Adults With Advanced Melanoma |
| 2033-04-01 | US | XENE | Xenon Pharmaceuticals Inc. | Phase 3 | An Open-label Study of XEN1101 in Epilepsy |
| 2033-05-01 | US | NRIX | Nurix Therapeutics, Inc. | Phase 2 | Study of NX-5948 in Combination With Other Agents in Adults With B-cell Malignancies |