Clinical Study

Pilot Study To Assess The Efficacy & Safety Of H.P. Acthar Gel In Subjects With Relapsing-Remitting Multiple Sclerosis

Posted Date: Aug 27, 2019

  • Investigator: Lawrence Goldstick
  • Specialties: Multiple Sclerosis, Neurology
  • Type of Study: Drug

This is a multicenter, multiple dose study to estimate the response rate, and examine the safety of H.P. Acthar Gel (Acthar) in subjects with RRMS who have not responded to high dose steroids.

Criteria:

Subjects With Rrms Who Have Experienced A Relapse And Who Will Receive 3 To 5 (Given Over A Period Of Up To 7 Days) Days Of Treatment With High Dose Steroids (Oral Or Iv) Within 28 Days Of The Onset Of Relapse Symptoms Are Candidates For The Current Study.

Keywords:

Relapsing-Remitting Multiple Sclerosis, Rrms, Ms

For More Information:

Sarah Hiti
937-535-5013
hitism@ucmail.uc.edu


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