drugset / Trial / NCT01023321

First-in-Human Single Ascending and Multiple Dose of GLPG0555

NCT01023321 ↗

Phase 1 Completed 35 enrolled Lakefront Biotherapeutics NV
RandomizedParallel-groupQuadruple-blind

Summary

The purpose of the study is to evaluate the safety and tolerability of single ascending (SAD) and multiple (MD) oral dose of GLPG0555 compared to placebo. Also, pharmacokinetics (PK) and pharmacodynamics (PD) of GLPG555 after single and multiple oral administration will be evaluated, and, if applicable, the maximum tolerated dose determined.

Timeline

Start
2009-12
Primary completion
2010-04
Completion
2010-05

Drugs

EvaluationDrugModalityDoseRoute
Subject GLPG0555 Unknown — Oral

Indications

No indication recorded.