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Study Evaluating Safety and Efficacy of Ropanicant in MDD Patients

Major Depressive Disorder Clinical Trial

Official title:
An Open-Label Study Evaluating the Safety and Efficacy of Ropanicant in Participants With Moderate to Severe Major Depressive Disorder

Clinical Trial 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).

Clinical Trial Description

Approximately 36 participants will be randomly assigned to receive ropanicant either 45 mg qd, 30 mg bid, or 45 mg bid for 2 weeks, in a ratio of 1:1:1 (12 participants in each treatment group). Following a screening period of up to 4 weeks, the participants will be treated for 2 weeks. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06126497
Study type Interventional
Source Suven Life Sciences Limited
Contact
Status Active, not recruiting
Phase Phase 2
Start date February 5, 2024
Completion date August 2024
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