drugset / Trial / NCT05938179

A Study of HS-10353 in Adult Participants With Major Depressive Disorder

NCT05938179 ↗

Phase 2 Unknown 144 enrolled Jiangsu Hansoh Pharmaceutical Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a randomized, double-blind, placebo-controlled Phase II clinical study to evaluate the efficacy and safety of continuous oral administration of HS-10353 in Chinese adults with depression.HS-10353 is a new generation of GABAA receptor isomeric modulator developed by our company, which can correct the dysfunction of GABAA receptor function and restore the balance between GABA receptor and NMDA receptor. Oral administration of HS-10353 at night for 14 days is expected to reduce clinical symptoms in patients with depression. As an oral preparation of allopregnenolone analogitics, it has good bioavailability, rapid onset and high safety, and has broad clinical application prospects, which is expected to better meet the treatment needs of clinical depression in China in the future.

Timeline

Start
2023-08-31
Primary completion
2024-11-01
Completion
2025-04-30

Drugs

EvaluationDrugModalityDoseRoute
Subject HS-10353 Unknown 30 mg Oral
Subject HS-10353 Unknown 50 mg Oral