A study to evaluate the efficacy and safety of Apremilast, Etanercept and placebo, in subjects with moderate to severe plaque psoriasis

Registry ID
EUCTR2012-000859-14
Source registry
EUCTR
Status
Completed
Phase
PHASE3
Sponsor
Celgene Corporation
Start date
2012-10-09
Completion date
2016-04-04
Last update
2026-08-16

Conditions

Summary

To evaluate the clinical efficacy and safety of oral apremilast 30 mg twice a day (BID) compared with placebo, in subjects with moderate to severe plaque psoriasis at Week 16

Locations

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