A Study to Investigate Adjunctive Treatment with Brenipatide Compared with Placebo in Delaying Time to Relapse in Adult Participants with Bipolar Disorder (RENEW-Bipolar-1)

Recruiting
99 years or below
All
Phase N/A
1 Location

Brief description of study

This study will evaluate the efficacy and safety of brenipatide vs placebo as an add-on to stable standard of care (SoC) in adults with BD I/II in remission or near remission with residual symptoms. The primary measure is time to relapse. The study includes Screening (~4 weeks), Double-Blind Treatment (until relapse/discontinuation/endpoint), and 8-week Safety Follow-Up. Visits occur about every 4 weeks.

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: Medical Research
  • Age: 99 years or below
  • Gender: All

TBD

Updated on 03 Dec 2025. Study ID: 25-1632

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