drugset / Trial / NCT01019070
Hepatic Impaired Subjects Compared to Healthy Subjects Receiving Multi-dose BMS-650032
Non-randomizedParallel-groupOpen-label
Summary
The purpose of this study is to assess the effects of hepatic impairment on the multiple dose pharmacokinetics of BMS-650032.
Timeline
- Start
- 2009-12
- Primary completion
- 2011-08
- Completion
- 2011-08
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Asunaprevir | Small molecule | 200 mg | Oral |