drugset / Trial / NCT06628362

A Study of Enicepatide (CT-388) in Participants Who Are Overweight or Obese With Type 2 Diabetes Mellitus

NCT06628362 ↗

Phase 2 Active not recruiting 447 enrolled Carmot Therapeutics, Inc. Hoffmann-La Roche · collab
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a multi-center, randomized, double-blind, placebo-controlled, parallel group dose-finding study to evaluate the efficacy and safety of enicepatide at low, middle, and high doses in participants who are overweight or obese with Type 2 diabetes mellitus (T2DM).

Timeline

Start
2024-11-21
Primary completion
2026-05-29
Completion
2026-09-24

Outcome

Met primary endpoint

release “In the study, enicepatide met both primary endpoints, delivering dose-dependent and clinically meaningful reductions in blood glucose and body weight at 48 weeks.” gene.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Enicepatide Unknown — Subcutaneous