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UnknownNCT06122181

Study of HS-10384 in Participants of Chinese Postmenopausal Women

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

Status
Unknown
Phase
Phase 1
Study type
Interventional
Enrollment
48 (estimated)
Sponsor
Hansoh BioMedical R&D Company · Industry
Sex
Female
Age
40 Years – 65 Years
Healthy volunteers
Accepted

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.

Detailed description

Phase Ib is consisted with 3\~4 multiple ascending doses.

Conditions

Interventions

TypeNameDescription
DRUGHS-10384 tabletsMultiple dosing of HS-10384 orally in a fasting state
DRUGHS-10384-matched placebo tabletsMultiple dosing of HS-10384-matched placebo orally in a fasting state

Timeline

Start date
2023-11-12
Primary completion
2024-06-30
Completion
2024-09-30
First posted
2023-11-08
Last updated
2024-03-13

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06122181. Inclusion in this directory is not an endorsement.