Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 45/100

Failure Rate

22.7%

102 terminated/withdrawn out of 449 trials

Success Rate

64.3%

-22.2% vs industry average

Late-Stage Pipeline

16%

74 trials in Phase 3/4

Results Transparency

96%

177 of 184 completed trials have results

Key Signals

100 recruiting177 with results83 terminated19 withdrawn

Enrollment Performance

Analytics

Phase 2
179(41.6%)
Phase 1
170(39.5%)
Phase 3
71(16.5%)
Early Phase 1
4(0.9%)
N/A
3(0.7%)
Phase 4
3(0.7%)
430Total
Phase 2(179)
Phase 1(170)
Phase 3(71)
Early Phase 1(4)
+2 more

Activity Timeline

Global Presence

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Clinical Trials (449)

Showing 20 of 449 trials
NCT06615050Phase 3Recruiting

A Study of Tacrolimus/Methotrexate/Ruxolitinib Versus Post-Transplant Cyclophosphamide/Tacrolimus/Mycophenolate Mofetil in Non-Myeloablative/Reduced Intensity Conditioning Allogeneic Peripheral Blood Stem Cell Transplantation (BMT CTN 2203)

Role: lead

NCT06610682Early Phase 1Recruiting

A Trial to Evaluate CSF ctDNA and Safety of Plixorafenib Alone or With Retifanlimab in Patients With BRAF-altered Glioma

Role: collaborator

NCT03570749Phase 2Completed

A Study of Baricitinib (LY3009104) in Participants With Severe or Very Severe Alopecia Areata

Role: collaborator

NCT07284849Phase 3Recruiting

A Study to Evaluate the Efficacy and Safety of Standard-of-Care Chemotherapy and Bevacizumab With or Without INCA33890 in the First-Line Treatment of Metastatic Microsatellite Stable Colorectal Cancer

Role: lead

NCT06959225Phase 3Recruiting

Study to Evaluate the Efficacy and Safety of Ruxolitinib Cream in Participants With Hidradenitis Suppurativa (TRuE-HS1)

Role: lead

NCT07214779Phase 3Recruiting

Study to Evaluate INCB123667 Versus Investigator's Choice of Chemotherapy in Participants With Platinum-Resistant Ovarian Cancer With Cyclin E1 Overexpression

Role: lead

NCT04859946Phase 2Active Not Recruiting

Itacitinib for the Prevention of Graft Versus Host Disease

Role: collaborator

NCT07356245Phase 2Recruiting

Ruxolitinib Maintenance Post-Hematopoietic Stem Cell Transplant T-Cell Lymphoma

Role: collaborator

NCT07441694Phase 1Recruiting

Study of INCA036978 in Participants With Myeloproliferative Neoplasms

Role: lead

NCT07124078Phase 2Recruiting

A Study to Evaluate Axatilimab Versus Best Available Therapy in Pediatric Participants With Chronic Graft-Versus-Host Disease After at Least 2 Prior Lines of Systemic Therapy (AGAVE-256)

Role: lead

NCT06516965Phase 3Active Not Recruiting

A Study to Evaluate the Efficacy and Safety Study of Povorcitinib in Participants With Prurigo Nodularis (STOP-PN2)

Role: lead

NCT07195916Phase 1Recruiting

A Study to Evaluate INCA036873 in Participants With Advanced Solid Tumors and Hematological Malignancies

Role: lead

NCT05238922Phase 1Recruiting

Study of INCB123667 in Subjects With Advanced Solid Tumors

Role: lead

NCT07023627Phase 2Recruiting

A Study of INCB123667 in Participants With Platinum-Resistant Ovarian Cancer With Cyclin E1 Overexpression

Role: lead

NCT07448155Phase 1Active Not Recruiting

A Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of INCA033989 Following Subcutaneous or Intravenous Administration in Healthy Adult Participants

Role: lead

NCT04577014Phase 1Recruiting

Retifanlimab (Anti-PD-1 Antibody) With Gemcitabine and Docetaxel in Patients With Advanced Soft Tissue Sarcoma

Role: collaborator

NCT05851443Phase 2Recruiting

A Study to Evaluate the Efficacy and Safety Study of Povorcitinib in Participants With Inadequately Controlled Moderate to Severe Asthma

Role: lead

NCT03069326Phase 2Active Not Recruiting

A Clinical Study to Test the Effects of Ruxolitinib And Thalidomide Combination for Patients With Myelofibrosis

Role: collaborator

NCT07522073Phase 3Recruiting

A Study to Evaluate Chemotherapy With or Without INCB161734 in Previously Untreated, KRAS G12D-Mutated Metastatic Pancreatic Ductal Adenocarcinoma

Role: lead

NCT06516952Phase 3Recruiting

A Study to Evaluate the Efficacy and Safety Study of Povorcitinib in Participants With Prurigo Nodularis (STOP-PN1)

Role: lead