A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multi-Center Phase 2 Study to Evaluate the Efficacy, Safety, and Tolerability of Once-Weekly CT-388 Administered Subcutaneously for 48 Weeks to Participants Who Are Overweight or Obese with Type 2 Diabetes Mellitus
Latest Information Update: 19 Jun 2025
At a glance
- Drugs CT-388 (Primary)
- Indications Type 2 diabetes mellitus
- Focus Therapeutic Use
- Sponsors Carmot Therapeutics
Most Recent Events
- 13 Jun 2025 Protocol amended to change the time frame form 48 week to 36 weeks.
- 13 Jun 2025 Planned End Date changed from 31 May 2026 to 30 Nov 2026.
- 13 Jun 2025 Planned primary completion date changed from 31 May 2026 to 10 Aug 2026.