HomeTrialNCT07310901
🔬NCT07310901Phase 1RECRUITING

A 2-part, Phase 1b Clinical Study Designed to Evaluate the Safety, PK, and Efficacy of CRB-913 in Participants With Obesity

Study Summary

This study will assess the safety of the investigational drug CRB-913 and how it is processed in the body. The study has two parts: Part 1 will measure drug levels in healthy adults after taking CRB-913 tablets, and Part 2 will compare three doses of CRB-913 with placebo to evaluate safety, effects on body weight, and drug levels in the blood. Part 2 is blinded, meaning participants, study doctors, and the sponsor will not know which treatment is given. Participants in Part 2 will take study treatment for 12 weeks and will be followed for 28 days after treatment ends.

Interventions / Drugs
View on ClinicalTrials.gov ↗
Study Details
Enrollment252 participants
Primary Completion
Lead SponsorCorbus Pharmaceuticals Inc.
Data Retrieved2026-04-11 04:10:39.232115+00:00
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