RecruitingPhase 1NCT07152288

Investigation of Pharmacokinetics,Safety,and Pharmacodynamics of HSK39297 in Subjects With Hepatic Impairment

A Single-dose, Open-label, Phase I Study Comparing the Pharmacokinetics, Safety, and Pharmacodynamics of HSK39297 in Subjects With Mild and Moderate Hepatic Impairment and Normal Hepatic Function


Sponsor

Haisco Pharmaceutical Group Co., Ltd.

Enrollment

24 participants

Start Date

May 29, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The study is being conducted to compare the pharmacokinetics, safety, and pharmacodynamics of HSK39297 in subjects with mild to moderate hepatic impairment and normal hepatic function


Eligibility

Min Age: 18 YearsMax Age: 70 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called HSK39297 tablets, a drug called HSK39297 tablets, and others for people with paroxysmal nocturnal hemoglobinuria, pnh. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years to 70 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGHSK39297 tablets

oral

DRUGHSK39297 tablets

oral

DRUGHSK39297 tablets

oral


Locations(1)

Peking University First Hospital

Beijing, China

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NCT07152288


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