Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

High Risk

Score: 80/100

Failure Rate

32.1%

9 terminated/withdrawn out of 28 trials

Success Rate

66.7%

-19.8% vs industry average

Late-Stage Pipeline

25%

7 trials in Phase 3/4

Results Transparency

0%

0 of 18 completed trials have results

Key Signals

9 terminated

Enrollment Performance

Analytics

Phase 2
13(46.4%)
Phase 3
7(25.0%)
Phase 1
7(25.0%)
N/A
1(3.6%)
28Total
Phase 2(13)
Phase 3(7)
Phase 1(7)
N/A(1)

Activity Timeline

Global Presence

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Clinical Trials (28)

Showing 20 of 28 trials
NCT02772718Phase 2Completed

An Open-Label Study of XOMA 358 in Patients With Hypoglycemia After Gastric Bypass Surgery

Role: lead

NCT00670592Phase 1Completed

Study of HCD122 in Adults With Non-Hodgkin's or Hodgkin's Lymphoma Who Have Progressed After at Least Two Prior Therapies

Role: collaborator

NCT02604485Phase 2Completed

A Single-Dose Open-Label Study of XOMA 358 in Subjects With Congenital Hyperinsulinism

Role: lead

NCT01747538Phase 3Terminated

Safety and Efficacy Study of Gevokizumab to Treat Non-infectious Uveitis Controlled With Systemic Treatment

Role: lead

NCT02315417Phase 3Terminated

An Efficacy and Safety Study of Gevokizumab in Treating Active Ulcers of Pyoderma Gangrenosum

Role: lead

NCT02326740Phase 3Terminated

An Efficacy and Safety Study of Gevokizumab in Treating Active Ulcers of Pyoderma Gangrenosum

Role: lead

NCT02318914Phase 3Terminated

A 2-Year, Open-Label, Safety Extension Study of Gevokizumab in Subjects With Pyoderma Gangrenosum

Role: lead

NCT01684345Phase 3Terminated

Safety and Efficacy Study of Gevokizumab to Treat Active Non-infectious Uveitis

Role: lead

NCT01882504Phase 2Completed

Proof of Concept Study of Gevokizumab in the Treatment of Pyoderma Gangrenosum

Role: lead

NCT01950312Phase 2Completed

The Effects of Gevokizumab in Corticosteroid-resistant Subjects With Autoimmune Inner Ear Disease

Role: lead

NCT00777816Phase 2Suspended

Safety and Pharmacokinetics Study of XOMA 052 in Subjects With Active, Stable, Moderate to Severe Rheumatoid Arthritis

Role: lead

NCT02258867Phase 3Terminated

Efficacy and Safety Study of Gevokizumab to Treat Behcet's Disease Uveitis

Role: lead

NCT02258854Phase 3Terminated

An Open-label, Rollover Study Providing Continued Dosing of Gevokizumab in Order to Assess Long-term Gevokizumab Safety Data

Role: lead

NCT02293564Not ApplicableCompleted

Open-label Safety Extension Study of Gevokizumab in Erosive Osteoarthritis of the Hand

Role: lead

NCT01683396Phase 2Completed

Safety and Biologic Activity Study of Gevokizumab to Treat Erosive Osteoarthritis of the Hand

Role: lead

NCT01498874Phase 2Completed

Efficacy and Safety Study of Gevokizumab to Treat Moderate to Severe Acne Vulgaris

Role: lead

NCT00998699Phase 2Completed

Study of the Effects of XOMA 052 on Insulin Production in Subjects With Well Controlled Type 1 Diabetes

Role: lead

NCT01882491Phase 2Completed

Safety and Biologic Activity Study of Gevokizumab to Treat Erosive Osteoarthritis of the Hand

Role: lead

NCT01788033Phase 2Completed

Effects of XOMA 052 on Insulin Production in Type 1 Diabetes

Role: collaborator

NCT00108108Phase 1Terminated

Dose-finding Trial of HCD122 in Patients With Chronic Lymphocytic Leukemia (CLL) That is Relapsed or Non-responsive to Prior Fludaribine Therapy

Role: collaborator