Key Insights

Highlights

Success Rate

84% trial completion

Published Results

48 trials with published results (23%)

Research Maturity

93 completed trials (45% of total)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 39/100

Termination Rate

8.7%

18 terminated out of 206 trials

Success Rate

83.8%

-2.7% vs benchmark

Late-Stage Pipeline

14%

29 trials in Phase 3/4

Results Transparency

52%

48 of 93 completed with results

Key Signals

48 with results84% success18 terminated

Data Visualizations

Phase Distribution

155Total
Not Applicable (37)
Early P 1 (9)
P 1 (16)
P 2 (64)
P 3 (23)
P 4 (6)

Trial Status

Completed93
Recruiting39
Active Not Recruiting20
Terminated18
Unknown16
Withdrawn10

Trial Success Rate

83.8%

Benchmark: 86.5%

Based on 93 completed trials

Clinical Trials (206)

Showing 20 of 20 trials
NCT04901195Phase 3Active Not RecruitingPrimary

A Study to Test the Long-term Treatment of Bimekizumab in Study Participants With Moderate to Severe Hidradenitis Suppurativa

NCT06768671Phase 3Active Not RecruitingPrimary

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

NCT07007637Phase 3Enrolling By InvitationPrimary

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

NCT03967600RecruitingPrimary

Clinical and Biological Characteristics of Hidradenitis Suppurativa

NCT07225569Phase 2RecruitingPrimary

A Study to Investigate Efficacy and Safety With SAR445399 in Adult Participants With Moderate to Severe Hidradenitis Suppurativa

NCT06888193Phase 1Recruiting

A Study to Assess the Concentration of Bimekizumab in Mature Breast Milk From Mothers Receiving Treatment With Bimzelx® (Bimekizumab)

NCT06015438Not ApplicableActive Not RecruitingPrimary

Physical Activity in Hidradenitis Suppurativa (HS)

NCT04115566RecruitingPrimary

Hidradenitis Suppurativa Prospective Observational Registry and Biospecimen Repository

NCT07228390Phase 2RecruitingPrimary

A 16-Week Study to Learn About the Study Medicine Called Ritlecitinib in Adults With Long Lasting Painful Red Skin Lumps, Known by the Medical Term, Hidradenitis Suppurativa, or HS.

NCT04414514Phase 2TerminatedPrimary

Topical Ruxolitinib 1.5% for Hidradenitis Suppurativa Treatment

NCT07547813Phase 2Not Yet RecruitingPrimary

A Proof-of-Concept Study of LAD328 in Adults With Hidradenitis Suppurativa

NCT06801795Not ApplicableActive Not RecruitingPrimary

Aviclear for Hidradenitis Suppurativa (HS)

NCT07543419RecruitingPrimary

Long Term Observational Study to Collect in a Real-world populatIon Data on the Treatment Pattern of Secukinumab in Adult Patients With Moderate to Severe HS Within the Italian Population

NCT06603077Phase 2CompletedPrimary

A Study to Evaluate the Efficacy and Safety of AVTX-009 in Patients With Moderate to Severe Hidradenitis Suppurativa

NCT06517732Active Not RecruitingPrimary

Study to Collect in a Real-world populatIon Data on the Treatment Pattern of Secukinumab in Adult Patients With Moderate to Severe Hidradenitis Suppurativa (HS) in Routine Clinical Practice in the Russian Federation

NCT06959225Phase 3RecruitingPrimary

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

NCT05921994Active Not RecruitingPrimary

Long Term Observational Study to Collect in a Real-world populatIon Data on the Treatment Pattern of secukinumAb in Adult Patients With Moderate to Severe Hidradenitis Suppurativa.

NCT04242498Phase 3CompletedPrimary

A Study to Evaluate the Efficacy and Safety of Bimekizumab in Study Participants With Moderate to Severe Hidradenitis Suppurativa

NCT07282015RecruitingPrimary

Real-world Secukinumab Outcomes in Canadian HS Patients

NCT04242446Phase 3CompletedPrimary

A Study to Evaluate the Efficacy and Safety of Bimekizumab in Study Participants With Moderate to Severe Hidradenitis Suppurativa

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