Comparative Bioavailability Study of Film-coated Tablet and Granule Formulations of RG1662

Summary

This study will compare the pharmacokinetic performance of film-coated tablet and granule formulations of RG1662 under fed and fasted conditions in healthy volunteers. A randomized, four-period, four-treatment crossover design is used. In each period, each volunteer will receive a single oral dose of the tablet or granule formulation either with or without food.

Timeline

Start

2014-08

Primary completion

2014-08

Completion

2014-08

Drugs

Indications

No indication recorded.