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Search / Trial NCT02398461

An Intravenous Infusion Study of rHIgM22 in Patients With Multiple Sclerosis Immediately Following a Relapse

Launched by ACORDA THERAPEUTICS · Mar 24, 2015

Trial Information

Current as of May 06, 2025

Completed

Keywords

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Males or females (18-70 years of age; \< 104 kg)
  • Capable of giving informed consent
  • Meet diagnostic criteria for MS, as defined by revised (2010) McDonald criteria
  • Present with a clinical acute relapse defined as a new or worsening neurological symptoms attributable to MS preceded by a stable or improving neurological state of at least 30 days, not associated with fever or infection, lasting at least 24 hours and accompanied by an objective physical (neurological) exam finding as confirmed by the Investigator
  • Has at least one new, identifiable, measurable and active lesion on MRI (Gd+) meeting the criteria of the imaging charter.
  • Exclusion Criteria:
  • Certain specified co-morbidities (including pregnancy)
  • Taking certain proscribed medications
  • A medical regimen that has changed in the month prior to screening
  • Inability to undergo requisite MRI evaluations
  • Drug or alcohol abuse
  • Any other reason for which, in the opinion of the Investigator, the subject should not participate in the study.

About Acorda Therapeutics

Acorda Therapeutics is a biotechnology company dedicated to developing innovative therapies for people with neurological disorders. Founded in 2004, the company focuses on advancing treatments that enhance the quality of life for patients with conditions such as multiple sclerosis and spinal cord injury. Acorda’s commitment to research and development drives its mission to bring transformative solutions to the market, leveraging cutting-edge science and clinical expertise. With a robust pipeline of therapies in various stages of development, Acorda Therapeutics aims to address unmet medical needs and improve patient outcomes through its rigorous clinical trial programs.

Locations

Long Beach, California, United States

Sacramento, California, United States

San Francisco, California, United States

Aurora, Colorado, United States

Centennial, Colorado, United States

Chicago, Illinois, United States

Saint Louis, Missouri, United States

Teaneck, New Jersey, United States

Rochester, New York, United States

Dallas, Texas, United States

Seattle, Washington, United States

Seattle, Washington, United States

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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