drugset / Trial / NCT06836063

Study to Evaluate Efficacy and Safety of Ropanicant in MDD Patients

NCT06836063 ↗

Phase 2 Completed 214 enrolled Suven Life Sciences Limited
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective is to evaluate the efficacy of Ropanicant at two different dosage levels compared to placebo in patients with Major Depressive Disorder (MDD).

Timeline

Start
2025-07-15
Primary completion
2026-02-23
Completion
2026-02-23

Drugs

EvaluationDrugModalityDoseRoute
Subject Ropanicant Small molecule — —