drugset / Trial / NCT02245841

Efficacy and Safety of H.P. Acthar Gel for the Treatment of Refractory Cutaneous Manifestations of Dermatomyositis

NCT02245841 ↗

Phase 4 Completed 19 enrolled The Cleveland Clinic Mallinckrodt · collab
NaSingle-groupOpen-labelTreatment

Summary

This study will assess the safety and efficacy of H.P. Acthar gel for treating the cutaneous manifestations in patients with refractory classic dermatomyositis, juvenile dermatomyositis, and amyopathic dermatomyositis. Our hypothesis is that H.P. Acthar gel will be both safe and effective for such patients.

Timeline

Start
2015-06-15
Primary completion
2021-07-14
Completion
2021-07-14

Outcome

Met primary endpoint

registry MEDIAN H.P Acthar Gel: -9 (-18 to -5) units on a scale NCT02245841 ↗

registry analysis (superiority test); H.P Acthar Gel; p < .001; Wilcoxon signed rank test NCT02245841 ↗

registry MEDIAN H.P Acthar Gel: -1.9 (-2.5 to -1.2) units on a scale NCT02245841 ↗

registry analysis (superiority test); H.P. Acthar Gel; p <0.001; Wilcoxon signed rank test NCT02245841 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Acthar Peptide 80 iu Subcutaneous