drugset / Trial / NCT06485401

To Compare the Safety and PK/ PD Characteristics of ADC189 Between Hepatic Impairment and Normal Hepatic Function Subjects

NCT06485401 ↗

Phase 1 Completed 16 enrolled Jiaxing AnDiCon Biotech Co.,Ltd
RandomizedParallel-groupOpen-labelTreatment

Summary

This study aims to evaluate the pharmacokinetics, pharmacodynamics, safety, and tolerability of ADC189 in subjects with hepatic impairment compared with subjects with normal hepatic function.

Timeline

Start
2024-03-14
Primary completion
2024-06-21
Completion
2024-06-21

Drugs

EvaluationDrugModalityDoseRoute
Subject ADC189 Unknown 45 mg Oral

Indications