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Tolerability of Acthar for the Treatment of Multiple Sclerosis in Relapses (TAMS)

Relapsing Remitting Multiple Sclerosis Clinical Trial

Official title:
Tolerability of Acthar for the Treatment of Multiple Sclerosis Relapses (TAMS)

Clinical Trial Summary

Tolerability of Acthar for the Treatment of Multiple Sclerosis Relapses (TAMS)

Clinical Trial Description

We propose to conduct a prospective, single-center, open-label, single-arm study comparing tolerability of Acthar versus oral prednisone in the treatment of MS relapses. Potential subjects will be identified during routine clinical evaluations. If patient is determined to be having a study-defined MS relapse, they will be invited to participate in this study. After consent is obtained, the patient will complete the first page of the ARMS survey. If prior steroid use was deemed tolerable then only the first page of the ARMS will be collected and analyzed and these patients will complete their participation in the trial. Their data from the ARMS will provide an estimate as to the number of patients who self-report tolerability and efficacy issues with steroids. However, if patients self-report prior steroid intolerability, then they will advance into the Acthar treatment arm of the trial. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02258217
Study type Interventional
Source OhioHealth
Contact
Status Completed
Phase N/A
Start date June 2014
Completion date December 2016
View Details
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