drugset / Trial / NCT01753401

Acthar for the Treatment of Systemic Lupus Erythematosus (SLE) in Patients With a History of Persistently Active Disease

NCT01753401

Phase 4 Completed 38 enrolled Mallinckrodt
RandomizedParallel-groupDouble-blindTreatment

Summary

This Phase 4 study is being performed to examine the effects of Acthar for the indicated use of treatment of SLE. This study will enroll patients with steroid-dependent, persistently active SLE with arthritic and/or cutaneous involvement. The study will involve two periods: an 8-week double-blind period, to provide placebo-controlled safety, efficacy, and pharmacodynamic data, and an optional open-label period, to examine the prolonged effects of Acthar maintenance.

Timeline

Start
2013-01
Primary completion
2015-10
Completion
2015-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Acthar Peptide 40 iu Subcutaneous
Subject Acthar Peptide 80 iu Subcutaneous