drugset / Trial / NCT06485401
To Compare the Safety and PK/ PD Characteristics of ADC189 Between Hepatic Impairment and Normal Hepatic Function Subjects
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | ADC189 | Unknown | 45 mg | Oral |