Clinical Trials Directory

Trials / Completed

CompletedNCT02143856

Oral Bioavailability of Solid Formulation of GLPG1205 With and Without Food

A Randomized, Open-label, Two-way Cross-over Study to Determine the Oral Bioavailability of GLPG1205 After Single-dose Intake in Healthy Male Subjects as a Solid Formulation, With and Without Food

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
12 (actual)
Sponsor
Galapagos NV · Industry
Sex
Male
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

The purpose of the study is to evaluate the amount of compound present in the blood (relative bioavailability) after a single oral administration of GLPG1205 given as a capsule formulation in fasted versus fed conditions in male healthy subjects. Also, the safety and tolerability of a single oral dose of GLPG1205 given as a capsule formulation under fasted and fed conditions will be assessed.

Conditions

Interventions

TypeNameDescription
DRUG100 mg GLPG1205A single dose of 100 mg GLPG1205 administered as two capsules of 50 mg

Timeline

Start date
2014-05-01
Primary completion
2014-07-01
Completion
2014-07-01
First posted
2014-05-21
Last updated
2014-07-22

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT02143856. Inclusion in this directory is not an endorsement.