Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Low Risk

Score: 25/100

Failure Rate

0.0%

0 terminated/withdrawn out of 10 trials

Success Rate

100.0%

+13.5% vs industry average

Late-Stage Pipeline

70%

7 trials in Phase 3/4

Results Transparency

0%

0 of 5 completed trials have results

Key Signals

1 recruiting

Enrollment Performance

Analytics

Phase 3
7(70.0%)
Phase 2
2(20.0%)
Phase 1
1(10.0%)
10Total
Phase 3(7)
Phase 2(2)
Phase 1(1)

Activity Timeline

Global Presence

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Clinical Trials (10)

Showing 10 of 10 trials
NCT06641089Phase 3Recruiting

Evaluation of Sonelokimab in Patients With Active Psoriatic Arthritis and Anti-TNFα Inadequate Response

Role: lead

NCT06641076Phase 3Active Not Recruiting

Evaluation of Sonelokimab in Patients With Active Psoriatic Arthritis Naive to Biologic Disease-Modifying Antirheumatic Drug

Role: lead

NCT07223138Phase 3Enrolling By Invitation

A Study to Evaluate the Long-term Safety, Tolerability, and Efficacy of Subcutaneous Sonelokimab in Participants With Psoriatic Arthritis

Role: lead

NCT07007637Phase 3Enrolling By Invitation

A Study to Evaluate the Long-term Safety, Tolerability, and Efficacy of Subcutaneous Sonelokimab in Participants With Moderate to Severe Hidradenitis Suppurativa

Role: lead

NCT06411899Phase 3Completed

A Study to Evaluate the Efficacy and Safety of Subcutaneous Sonelokimab Compared With Placebo in Adult Participants With Moderate to Severe Hidradenitis Suppurativa

Role: lead

NCT06411379Phase 3Completed

Study to Evaluate the Efficacy and Safety of Subcutaneous Sonelokimab Compared With Placebo in Adult Participants With Moderate to Severe Hidradenitis Suppurativa

Role: lead

NCT06768671Phase 3Active Not Recruiting

An Open-label, Single-arm Study to Evaluate Pharmacokinetics and Safety of Subcutaneous Sonelokimab in Adolescents With Moderate to Severe Hidradenitis Suppurativa (VELA-TEEN)

Role: lead

NCT06994936Phase 1Completed

An Open-label Study in Healthy Adults to Evaluate the Relative Bioequivalence of a Single-dose Administration of Sonelokimab Either by a Prefilled Syringe or an Autoinjector

Role: lead

NCT05640245Phase 2Completed

Evaluation of Sonelokimab for the Treatment of Patients With Active Psoriatic Arthritis

Role: lead

NCT05322473Phase 2Completed

Evaluation of Sonelokimab for the Treatment of Patients With Active Moderate to Severe Hidradenitis Suppurativa

Role: lead

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