LivingGLP1
Study S002644

A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group 52-Week Trial to Investigate the Efficacy and Safety of Olatorepatide, a GLP-1/GIP Receptor Agonist, in Adults With Moderate to Severe Hidradenitis Suppurativa Living With Overweight or Obesity

Registration

Registration
NCT07830329
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
QUADRUPLE
Status
NOT_YET_RECRUITING
Enrollment
300
Start
2026-10-30
Primary completion
2028-11-24
Lead sponsor
Regeneron Pharmaceuticals
Conditions
Hidradenitis Suppurativa
Interventions
DRUG:Olatorepatide; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
CTIS:2026-526375-39-00

Registered primary outcomes

  • Percent change in total Abscess and inflammatory Nodule (AN) count [From baseline to week 52]

Linked records (0)

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