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A Phase 2, Randomized, Placebo-controlled, Double-blind Study of EG017 in Female Patients With Stress Urinary Incontinence

Stress Urinary Incontinence Clinical Trial

Official title:
A Multicenter, Randomized, Double-blind, Placebo-controlled, Dose-exploration Phase II Trial to Evaluate the Efficacy and Safety of EG017 Tablets in Postmenopausal Women With Stress Urinary Incontinence

Clinical Trial Summary

The purpose of this study is to determine whether EG017 is safe and effective in the treatment of stress urinary incontinence in postmenopausal women.

Clinical Trial Description

The main purpose of this study is to assess the efficacy of EG017 in female patients with stress urinary incontinence (SUI) compared with placebo as measured by the percent change in the urinary incontinence volume measured in a 1-hour pad test from baseline at week 12. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05674045
Study type Interventional
Source GeneScience Pharmaceuticals Co., Ltd.
Contact
Status Completed
Phase Phase 2
Start date January 6, 2022
Completion date September 26, 2022
View Details
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