Bioavailability Study of BIA 5-453

Status Completed

Clinical Trial Summary

The purpose of this study was to compare the bioavailability and tolerability of BIA 5-453 under fasted and fed conditions.

Clinical Trial Description

This was a Single-centre, two-way crossover, randomised, open-label study in 12 healthy male volunteers. Subjects received a single oral 200 mg dose of BIA 5-453 following a standard meal in one period, and following at least 10 hours of fasting in another period. Treatment periods were separated by a washout interval of 2 weeks or more. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03090568
Study type	Interventional
Source	Bial - Portela C S.A.
Contact
Status	Completed
Phase	Phase 1
Start date	July 15, 2008
Completion date	August 14, 2008

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