drugset / Trial / NCT06726850

Clinical Study to Evaluate the Efficacy and Safety of GS1-144 Tablets in the Treatment of Moderate to Severe Vasomotor Symptoms in Chinese Postmenopausal Women.

NCT06726850 ↗

Phase 2 Completed 129 enrolled Changchun GeneScience Pharmaceutical Co., Ltd.
RandomizedParallel-groupDouble-blindTreatment

Summary

A Randomized, Double-blind, Placebo-controlled, Parallel-group Phase II Clinical Study to Evaluate the Efficacy and Safety of GS1-144 Tablets in the Treatment of Moderate to Severe Vasomotor Symptoms in Chinese Postmenopausal Women.

Timeline

Start
2024-10-14
Primary completion
2025-04-17
Completion
2025-07-29

Outcome

Met primary endpoint

release “GS1-144 reduced both the frequency and severity of moderate-to-severe VMS in Chinese postmenopausal women.” genscigroup.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject GS1-144 Unknown — —

Indications