drugset / Trial / NCT07412756

A Study of Brenipatide in Adult Participants With Major Depressive Disorder

NCT07412756 ↗

Phase 3 Recruiting 1000 enrolled Eli Lilly and Company
RandomizedParallel-groupDouble-blindTreatment

Summary

This study evaluates the safety and efficacy of brenipatide when administered with standard of care (SoC) compared to placebo plus SoC in delaying the return of major depressive symptoms. The trial is divided into four periods as follows: a screening period that will last approximately 1 month, a treatment period with a potential post treatment period that combined will last a minimum of 12 months, and the follow up period that will last approximately 2 months.

Timeline

Start
2026-02-09
Primary completion
2028-02
Completion
2028-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Brenipatide Unknown — Subcutaneous