A Phase II Study of HS-10353 in Participants With Postpartum Depression

Status Not yet recruiting

Clinical Trial Summary

The primary purpose of this study is to determine if treatment with HS-10353 reduces depressive symptoms in participants with postpartum depression (PPD) compared to placebo as assessed by the change from baseline in the 17-item Hamilton Rating Scale for Depression (HAM-D17) total score at Day 15. And the secondary purpose of this study is to evaluate the safety and tolerability of HS-10353 compared to placebo as assessed by the incidence of adverse events, clinical laboratory evaluations, electrocardiogram (ECG) parameters, the Columbia Suicide Severity Rating Scale (C-SSRS), and the 20-item Physician Withdrawal Checklist (PWC-20).

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05937867
Study type	Interventional
Source	Jiangsu Hansoh Pharmaceutical Co., Ltd.
Contact	Yun Chen
Phone	18652105250
Email	cheny22@hspharm.com
Status	Not yet recruiting
Phase	Phase 2
Start date	August 31, 2023
Completion date	October 31, 2025

View Details

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