drugset / Trial / NCT01208753

Pharmacokinetics/Pharmacodynamics (PK/PD) of Multiple Oral Doses of GLPG0555 in Healthy Subjects

NCT01208753 ↗

Phase 1 Completed 24 enrolled Lakefront Biotherapeutics NV
RandomizedParallel-groupQuadruple-blind

Summary

The purpose of the study is to evaluate the safety and tolerability of multiple ascending oral doses (MAD) of GLPG0555 given to healthy subjects for 13 days compared to placebo, and to evaluate the relative bioavailability and pharmacokinetics (PK) of two different aqueous suspensions of GLPG0555 administered for 3 days. Finally, it is aimed to characterize PK and pharmacodynamics (PD) of GLPG0555 after multiple oral administrations.

Timeline

Start
2010-09
Primary completion
2010-11
Completion
2011-02

Drugs

EvaluationDrugModalityDoseRoute
Subject GLPG0555 Unknown 50 mg Oral
Subject GLPG0555 Unknown 100 mg Oral

Indications

No indication recorded.