drugset / Trial / NCT01186588
A Study of Canagliflozin in Study Participants With Various Degrees of Impaired Hepatic (Liver) Function
Non-randomizedParallel-groupOpen-label
Summary
The purpose of the study is to determine the concentration of canagliflozin in blood and urine samples after the administration of canagliflozin to study participants with mild or moderate hepatic (liver) impairment compared with study participants with normal hepatic function.
Timeline
- Start
- 2010-08
- Primary completion
- 2011-04
- Completion
- 2011-04
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | CANAGLIFLOZIN ANHYDROUS | Small molecule | 300 mg | Oral |