Clinical Trials Directory

Trials / Completed

CompletedNCT01024517

GLPG0259 Solid Formulation Bioavailability and Food Effect

An Open Label Study to Compare the Oral Bioavailability of a Solid Dose Formulation of GLPG0259 Relative to an Oral Solution After Single-dose Intake in Healthy Subjects and to Evaluate the Effect of Food on the Solid Dose Formulation.

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 compare the pharmacokinetics of GLPG0259 as a solid dosage formulation (with and without food)and an oral solution, and to assess its safety and tolerability.

Conditions

Interventions

TypeNameDescription
DRUGGLPG0259 solutionsingle oral dose, GLPG0259, 50 mg oral solution
DRUGGLPG0259single oral dose, GLPG0259, 50 mg solid formulation

Timeline

Start date
2009-11-01
Primary completion
2009-12-01
Completion
2010-02-01
First posted
2009-12-02
Last updated
2010-04-27

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT01024517. Inclusion in this directory is not an endorsement.