Study S000893
Investigation of Pharmacokinetics and Safety of HRS-7535 in Subjects With Mild and Moderate Hepatic Impairment and Normal Hepatic Function
Registration
Registered primary outcomes
- The maximum plasma concentration of HRS-7535 (Cmax) [Post-dose at day 1 to day 4.]
- Area under the concentration curve from time 0 to the last quantifiable concentration (AUC0-t) [Post-dose at day 1 to day 4.]
- Area under the concentration curve from time 0 to extrapolated infinite time (AUC0-inf) [Post-dose at day 1 to day 4.]
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