drugset / Trial / NCT01535638
Bioavailability of 3 Different Formulations of BI 207127 in Healthy Male Volunteers
RandomizedCrossoverOpen-labelTreatment
Summary
The primary objective of the current study is to investigate the relative bioavailability of three trial formulations of BI 207127, the trial formulation 2 (TFII), the final formulation (FF), and a FF modified formulation. All formulations are supplied as film-coated Tablets and administered as single dose treatments of BI 207127 (3 film-coated Tablets) in healthy volunteers, with the aim to compare the bioavailability of the three formulations. All treatments will be applied fed, 30 minutes after start of the intake of a standard normal breakfast.
Timeline
- Start
- 2012-02
- Primary completion
- 2012-03
- Completion
- —
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Deleobuvir | Small molecule | — | Oral |
Indications
No indication recorded.