Clinical Trials Directory

Trials / Completed

CompletedNCT01915667

Oral Bioavailability of Two Solid Formulations of GLPG0634

Bioavailability Study Comparing Two Solid Oral Formulations of GLPG0634 in Healthy Male Subjects

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
12 (actual)
Sponsor
Galapagos NV · Industry
Sex
Male
Age
40 Years – 60 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 administration of GLPG0634 as a tablet versus a capsule in fasted conditions in male healthy subjects. Also, the effect of food on the bioavailability of the tablet formulation will be studied as well as the safety and tolerability of single oral doses of GLPG0634 given either as capsule or tablet.

Conditions

Interventions

TypeNameDescription
DRUG200 mg GLPG0634 as capsules, fastedsingle oral dose of 200 mg GLPG0634 given as capsules in fasted condition
DRUG200 mg GLPG0634 as tablets, fastedsingle oral dose of 200 mg GLPG0634 given as tablets in fasted condition
DRUG200 mg GLPG0634 as tablets, fedsingle oral dose of 200 mg GLPG0634 given as tablets in fed condition

Timeline

Start date
2013-07-01
Primary completion
2013-09-01
Completion
2013-09-01
First posted
2013-08-05
Last updated
2013-09-17

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT01915667. Inclusion in this directory is not an endorsement.