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A Study of Brenipatide in Adult Participants With Major Depressive Disorder

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NCT07412756 · readout ≤ 559 d

Sponsored by Eli Lilly and Company (industry) · LLY — their whole pipeline →.

Phase
Phase 3
Status
Recruiting
Study type
Interventional
Design
Randomized · Double · Treatment
Enrollment
1,000estimated
Sites
179
Countries
Australia, Brazil, Canada +12

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2026-02-09actualWhen the study began enrolling
Primary completionFeb 2028estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionFeb 2028estimatedThe whole study's end, after follow-up
First posted2026-02-17actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-06actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Depressive Disorder, Major

Interventions

  • Drug: Brenipatide — also filed as LY3537031
  • Drug: Placebo

Primary outcome

what the primary-completion date above is the date OF
Time to Relapse Defined as the Number of Days from Randomization to Date on Which the Participant Meets Any Relapse Criterion of Major Depressive Disorder (MDD)
measured From Randomization in Double-Blind Adjunctive Treatment to First Relapse For at Least 12 Months

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