drugset / Trial / NCT06354660

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)

NCT06354660

Phase 3 Completed 537 enrolled Eli Lilly and Company
RandomizedParallel-groupDouble-blindTreatment

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.

Timeline

Start
2024-04-10
Primary completion
2026-01-22
Completion
2026-02-20

Drugs

EvaluationDrugModalityDoseRoute
Subject Retatrutide Protein / enzyme biologic 4 mg Subcutaneous
Subject Retatrutide Protein / enzyme biologic 9 mg Subcutaneous
Subject Retatrutide Protein / enzyme biologic 12 mg Subcutaneous