Clinical Trial

A Pharmacokinetic and Safety Study of MY008211A Tablets in Subjects With Impaired or Normal Hepatic Function

Completed Phase 1
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Summary
This study is a single-center, non-randomized, open-label, parallel, single-dose study to evaluate the PK profile and safety of MY008211A Tablets in subjects with hepatic impairment.
Trial Details
NCT Number NCT07625618
Lead Sponsor Wuhan Createrna Science and Technology Co., Ltd
Conditions Hepatic Insufficiency (MeSH ID: D048550)
Enrollment 24 participants
Start Date 2024-09-20
Primary Completion 2024-12-28 (estimated)
Study Completion 2024-12-28 (estimated)
Updated on ClinicalTrials.gov 2026-06-04