Study Complete
Sponsor ID
CC-10004-CP-022

Effect of Food on the Pharmacokinetics of Apremilast (CC-10004) in Healthy Subjects

Sponsor ID
CC-10004-CP-022
Clinicaltrials.gov ID
NCT01634178
EUCTIS ID
N/A
EudraCT ID
N/A

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.

Additional Study Details

Phase
Phase 1
Product
N/A
Type
Interventional
Masking
None (Open Label)
Enrollment
46
Additional Study Details

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
Status
Contact Us
Location
PPD Development
Austin, TX, United States, 787844
Status
Completed