Study Evaluating Safety and Efficacy of Ropanicant in MDD Patients
NCT06126497 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 41
Last updated 2026-04-08
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).
Conditions
Interventions
- DRUG
-
Ropanicant
Tablet
Sponsors & Collaborators
-
Suven Life Sciences Limited
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-02-05
- Primary Completion
- 2024-07-19
- Completion
- 2024-07-19
- FDA Drug
- Yes
Countries
- United States
Study Locations
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