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

2014-08-27 03:17:37 | BioPortfolio

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.

Study Design

Allocation: Randomized, Control: Placebo Control, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)

Conditions

Healthy

Intervention

GLPG0555, placebo, GLPG0555, placebo

Location

SGS Stuivenberg
Antwerp
Belgium

Status

Completed

Source

Galapagos NV

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:17:37-0400

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