drugset / Trial / NCT01906372

Acthar in Treatment of Refractory Dermatomyositis and Polymyositis

NCT01906372

Phase 2 Completed 12 enrolled Rohit Aggarwal, MD Mallinckrodt · collab
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this research study is to evaluate the effectiveness of the study drug, ACTH Gel in people diagnosed with dermatomyositis a disease that causes muscle weakness and is associated with a rash (DM) or polymyositis (PM) a disease that causes muscle weakness without a rash. The study doctors want to evaluate whether ACTH Gel will improve the symptoms of this disease. This drug is approved by the Food and Drug Administration (FDA) for dermatomyositis (DM) and polymyositis (PM). ACTH gel has been an FDA-approved treatment for myositis since 1952, and in 2010 the FDA retained PM and DM as diseases approved for ACTH gel use.

Timeline

Start
2013-09
Primary completion
2015-09
Completion
2016-05

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Adrenocorticotropin Protein / enzyme biologic 80 iu Intramuscular

Indications