drugset / Trial / NCT06126497

Study Evaluating Safety and Efficacy of Ropanicant in MDD Patients

NCT06126497 ↗

Phase 2 Completed 41 enrolled Suven Life Sciences Limited
RandomizedParallel-groupOpen-labelTreatment

Summary

This is an open-label, parallel-group study to evaluate the safety and efficacy of ropanicant in participants with moderate to severe Major Depressive Disorder (MDD).

Timeline

Start
2024-02-05
Primary completion
2024-07-19
Completion
2024-07-19

Drugs

EvaluationDrugModalityDoseRoute
Subject Ropanicant Small molecule 1 unknown —
Subject Ropanicant Small molecule 2 unknown —
Subject Ropanicant Small molecule 3 mg —