drugset / Trial / NCT00773734

Efficacy and Safety Study of Apremilast (CC-10004) in Subjects With Moderate-to-Severe Plaque-Type Psoriasis (Core Study)

NCT00773734 ↗

Phase 2 Completed 352 enrolled Amgen
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study was to test if the drug apremilast was safe, if it helped improve psoriasis, and how well the participants tolerated it.

Timeline

Start
2008-09-01
Primary completion
2009-08-01
Completion
2015-05-20

Outcome

Met primary endpoint

registry Placebo BID vs Apremilast 20mg BID; p <0.0001; Risk Difference (RD) 23.1 (95% CI 12.4 to 33.7) NCT00773734 ↗

registry Placebo BID vs Apremilast 30 mg BID; p <0.0001; Risk Difference (RD) 35.2 (95% CI 23.9 to 46.6) NCT00773734 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Apremilast Small molecule 10 mg Oral
Subject Apremilast Small molecule 20 mg Oral
Subject Apremilast Small molecule 30 mg Oral

Indications