drugset / Trial / NCT06029439

Study to Assess the Safety and Effectiveness of NMRA-335140-501

NCT06029439 ↗

Phase 3 Active not recruiting 1000 enrolled Neumora Therapeutics, Inc.
NaSingle-groupOpen-labelTreatment

Summary

This is a 52-week open-label extension (OLE) study that will evaluate the safety, tolerability, and effectiveness of NMRA-335140 in participants with major depressive disorder (MDD). Participants who completed a parent study investigating the efficacy and safety of NMRA-335140 as a treatment for MDD (ie, NMRA-335140-301, NMRA-335140-302, or NMRA-335140-303), and complete the 6 weeks double-blind treatment, provide informed consent, and meet eligibility criteria, may enter this extension study.

Timeline

Start
2023-11-10
Primary completion
2027-06
Completion
2027-06

Drugs

EvaluationDrugModalityDoseRoute
Subject NMRA-335140 Small molecule 80 mg Oral