drugset / Trial / NCT04859426
A Study to Evaluate the Pharmacokinetics and Safety of DBPR108 in Subjects With Hepatic Impairment
Non-randomizedParallel-groupOpen-labelTreatment
Summary
This is an open-label, single-dose study to evaluate the pharmacokinetics and safety of DBPR108 in subjects with mild or moderate hepatic impairment (HI) compared to the matched control subjects with normal hepatic function.
Timeline
- Start
- 2021-06-09
- Primary completion
- 2022-05-14
- Completion
- 2022-05-17
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | DBPR108 | Small molecule | 100 mg | Oral |
Indications
No indication recorded.