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Clinical Trial Summary

This is a randomized study exploring the efficacy, safety and steroid sparing ability of two doses (40 U and 80 U) of Acthar in SLE patients with immune mediated hematologic manifestations requiring steroid use for a minimum of 2 weeks prior to screening.


Clinical Trial Description

Acthar is currently labeled for use during an exacerbation or for maintenance therapy in selected SLE cases, however data from prospective trials on hematologic manifestations of SLE are not available. Due to the potential effect of lowering or eliminating autoantibodies, the absence of bone marrow suppression, and a steroid sparing effect, Acthar may represent a novel therapeutic option in recalcitrant cases of hematologic SLE. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02779153
Study type Interventional
Source NYU Langone Health
Contact
Status Withdrawn
Phase Phase 4
Start date October 2016
Completion date May 22, 2019

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