Study Complete
Sponsor ID
CC-10004-CP-022
Effect of Food on the Pharmacokinetics of Apremilast (CC-10004) in Healthy Subjects
Study Details
The purpose of the study is to evaluate the effects of a high fat meal on the pharmacokinetics of a single dose of 30 mg of apremilast in healthy subjects.
Protocol Summary
Primary Outcome Measures
AUC0-24
Timeframe: Up to 15 days
Cmax
Timeframe: Up to 15 days
Tmax
Timeframe: Up to 15 days
AUC0-t
Timeframe: Up to 15 days
AUC0–∞
Timeframe: Up to 15 days
t1/2
Timeframe: Up to 15 days
Secondary Outcome Measures
Number of participants with Adverse Events
Timeframe: Up to 22 days
Locations
Location
PPD Development
Austin, TX, United States, 787844
Status
Completed