CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 537 enrolled
Drug / intervention
Retatrutide +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06354660
NCT06354660Phase 3Completed

A Phase 3, Randomized, Multicenter, Double-Blind Study to Investigate the Efficacy and Safety of Retatrutide Once Weekly Compared With Placebo in Adult Participants With Type 2 Diabetes and Inadequate Glycemic Control With Diet and Exercise Alone (TRANSCEND-T2D-1)

Eli Lilly and Company·interventional·Posted Apr 9, 2024·Updated Mar 5, 2026

In Brief

A Phase 3 clinical trial evaluating Retatrutide and Placebo for Diabetes Type 2. Completed, enrolled 537 participants across 48 sites in 4 countries.

Detailed Summary

The purpose of this study is to investigate the efficacy and safety of retatrutide compared with placebo in participants with Type 2 Diabetes and inadequate glycemic control. The study will last about 11 months and may include up to 11 visits.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsDiabetes Type 2
CountriesIndia, Mexico, Puerto Rico, United States
Collaborators--

Timeline

Phase 3CompletedFinished
20252026
First PostedApr 9, 2024
Enrollment StartApr 10, 2024
Primary CompletionJan 22, 2026
Study CompletionFeb 20, 2026
TodayJul 2, 2026
Enrollment to primary: 1.8 yearsPosted 2.2 years ago

Interventions

Retatrutidedrug

Administered SC.

Placebodrug

Administered SC.