drugset / Trial / NCT06029426

Study to Evaluate the Effects of Oral NMRA-335140 Versus Placebo in Participants With Major Depressive Disorder

NCT06029426 ↗

Phase 3 Completed 383 enrolled Neumora Therapeutics, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a randomized, double blind, placebo controlled, multi-center study to evaluate the effects of NMRA-335140 (formerly BTRX 335140) on symptoms of depression in participants with Major Depressive Disorder (MDD). The study design consists of a Screening Period (up to 28 days), and a 6-week Treatment Period (during which participants will receive either NMRA-335140 or placebo). At the completion of the 6-week Treatment Period, participants who complete the study, provide informed consent, and meet the eligibility criteria may enter an extension study (NMRA-335140 501).

Timeline

Start
2023-09-20
Primary completion
2024-12-03
Completion
2025-01-15

Drugs

EvaluationDrugModalityDoseRoute
Subject NMRA-335140 Small molecule 80 mg Oral