drugset / Trial / NCT03161483

A Study to Evaluate the Efficacy and Safety of CC-220 in Subjects With Active Systemic Lupus Erythematosus

NCT03161483 ↗

Phase 2 Completed 289 enrolled Celgene Corporation
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this Phase 2, multicenter, randomized, placebo-controlled, double-blind study to evaluate the efficacy and safety of an oral treatment regimen of CC-220 versus placebo in adult subjects with active systemic lupus erythematosus. Approximately 280 subjects with a documented diagnosis of SLE will be randomized 2:2:1:2 to receive CC-220 (0.45 mg QD, 0.3 mg QD or 0.15 mg QD) or identically appearing placebo.

Timeline

Start
2017-08-31
Primary completion
2021-08-03
Completion
2021-08-03

Outcome

Met primary endpoint

registry PBO QD vs 0.45 mg QD; p = 0.011; Stratified difference 19.4 (95% CI 4.12 to 33.42) NCT03161483 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Iberdomide Small molecule 0.15 mg Oral
Subject Iberdomide Small molecule 0.3 mg Oral
Subject Iberdomide Small molecule 0.45 mg Oral