drugset / Trial / NCT06393673

A Study to Find the Best Dose of HS-10384 to Treat Vasomotor Symptoms in Postmenopausal Women

NCT06393673 ↗

Phase 2 Unknown 195 enrolled Hansoh BioMedical R&D Company
RandomizedParallel-groupDouble-blindTreatment

Summary

A randomized, double-blind, placebo-controlled phase 2 clinical study to evaluate the efficacy and safety of HS-10384 in postmenopausal women suffering from vasomotor symptoms.

Timeline

Start
2024-05-30
Primary completion
2025-06-30
Completion
2025-09-30

Drugs

EvaluationDrugModalityDoseRoute
Subject HS-10384 Unknown — Oral

Indications

No indication recorded.