drugset / Trial / NCT06122181

Study of HS-10384 in Participants of Chinese Postmenopausal Women

NCT06122181 ↗

Phase 1 Unknown 48 enrolled Hansoh BioMedical R&D Company
RandomizedSequentialDouble-blindTreatment

Summary

A randomized, double-blind, placebo-controlled phase Ib clinical study to evaluate the safety, tolerability and pharmacokinetics characteristics of HS-10384 in Chinese postmenopausal women.

Timeline

Start
2023-11-12
Primary completion
2024-06-30
Completion
2024-09-30

Drugs

EvaluationDrugModalityDoseRoute
Subject HS-10384 Unknown — Oral

Indications

No indication recorded.