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
| Type | Name | Description |
|---|---|---|
| DRUG | 100 mg GLPG1205 | A 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.