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RE104 Safety and Efficacy Study in Postpartum Depression

Postpartum Depression Clinical Trial

Official title:
A Multicenter, Randomized, Double-Blind, Parallel-Group Dose-Controlled Study Evaluating the Safety and Efficacy of RE104 for Injection in the Treatment of Patients With Postpartum Depression (PPD)

Clinical Trial Summary

The purpose of this study is to determine if treatment with a single dose of RE104 for Injection reduces depressive symptoms in participants with moderate-to-severe postpartum depression (PPD) as compared to active-placebo.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06342310
Study type Interventional
Source Reunion Neuroscience Inc
Contact Jasna Hocevar-Trnka, M.D.
Phone 1-888-880-REUN
Email info@reunionneuro.com
Status Recruiting
Phase Phase 2
Start date June 14, 2024
Completion date June 2025
View Details
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