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.

PHASE2RecruitingINTERVENTIONAL
Enrollment

129

Participants

Timeline

Start Date

September 2, 2022

Primary Completion Date

January 30, 2025

Study Completion Date

June 30, 2025

Conditions
Vasomotor Syndrome
Interventions
DRUG

Placebo

In the placebo arm, participants will consume a placebo matching GenSci1-144 for 12 consecutive weeks.

DRUG

GS1-144

In the GS1-144 arm, participants will receive multiple doses of GS1-144 tablets for 12 consecutive weeks

Trial Locations (1)

100730

RECRUITING

Peking Union Medical College Hospital, Beijing

All Listed Sponsors
lead

Changchun GeneScience Pharmaceutical Co., Ltd.

INDUSTRY