GLPG0778: Multiple Ascending Oral Doses, Pharmacokinetic, Safety, and Pharmacodynamic Study
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|ClinicalTrials.gov Identifier: NCT01336244|
Recruitment Status : Completed
First Posted : April 15, 2011
Last Update Posted : October 18, 2011
|Condition or disease||Intervention/treatment||Phase|
|Healthy||Drug: GLPG0778 Drug: placebo||Phase 1|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||45 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|
|Official Title:||Double Blind Placebo Controlled Dose Ranging Study for the Assessment of Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Multiple Ascending Oral Doses of GLPG0778 in Healthy Male Subjects|
|Study Start Date :||April 2011|
|Actual Primary Completion Date :||August 2011|
|Actual Study Completion Date :||September 2011|
Experimental: GLPG0778 ascending doses
Multiple ascending doses for 13 days, ranging from 50 mg twice daily upto a maximum to be determined during escalation.
capsules containing 50 or 100 mg of GLPG0778
Placebo Comparator: Placebo
Twice daily for 13 days, matching the scheme of the multiple ascending dose.
multiple dose, aqueous formulation, 13 days days, matching ascending dose schedule
- Occurrence of adverse events [ Time Frame: Daily during treatment, up to 10 days postdose ]At every study visit, subjects will be asked whether any adverse events have occurred since start of treatment.
- Evaluation of hematological, biochemical and cardiovascular parameters. [ Time Frame: until 10 days postdose. ]On predefined timepoints during the study blood and urine samples will be taken, and cardiovascular tests (ECG, blood pressure, heart rate) recorded to assess whether the test compound causes any deviation.
- Pharmacokinetics of repeated doses [ Time Frame: 24 hours postdose ]Bloodsamples are taken on various timepoints to assess how much of the study drug is taken up in the blood (absorption), how long it stays in the blood (excretion), and whether any "breakdown"-products of the drug are present (metabolism).
- Pharmacodynamics (PD) of GLPG0778 [ Time Frame: up to 10 days postdose ]To explore biomarkers of GLPG0778 activity after repeated oral administrations.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01336244
|Study Director:||Gerben van 't Klooster, PhD||Galapagos NV|
|Principal Investigator:||Lien Gheyle, MD||SGS Stuivenberg|