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.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
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
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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