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Trials / Completed

CompletedNCT06354660

Effect of Retatrutide Compared With Placebo in Adult Participants With Type 2 Diabetes and Inadequate Glycemic Control With Diet and Exercise Alone (TRANSCEND-T2D-1)

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)

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
537 (actual)
Sponsor
Eli Lilly and Company · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGRetatrutideAdministered SC.
DRUGPlaceboAdministered SC.

Timeline

Start date
2024-04-10
Primary completion
2026-01-22
Completion
2026-02-20
First posted
2024-04-09
Last updated
2026-03-05

Locations

48 sites across 4 countries: United States, India, Mexico, Puerto Rico

Regulatory

Source: ClinicalTrials.gov record NCT06354660. Inclusion in this directory is not an endorsement.

Effect of Retatrutide Compared With Placebo in Adult Participants With Type 2 Diabetes and Inadequate Glycemic Control W (NCT06354660) · Clinical Trials Directory