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
| Type | Name | Description |
|---|---|---|
| DRUG | 200 mg GLPG0634 as capsules, fasted | single oral dose of 200 mg GLPG0634 given as capsules in fasted condition |
| DRUG | 200 mg GLPG0634 as tablets, fasted | single oral dose of 200 mg GLPG0634 given as tablets in fasted condition |
| DRUG | 200 mg GLPG0634 as tablets, fed | single 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.