Multiple Sclerosis Clinical Trial

A Multicenter Study to Assess the Effect of Plasma Exchange in Accelerating the Clearance of Natalizumab in Subjects With Multiple Sclerosis (MS)

Summary

Natalizumab (TYSABRI) is a protein-based drug that is manufactured by Biogen Idec in partnership with Elan Pharmaceuticals. Natalizumab is approved in the US and Europe for the treatment of Multiple Sclerosis (MS). The purpose of this study is to determine whether the amount of natalizumab (TYSABRI) that is present in your blood (plasma) can be reduced or eliminated by separating and removing the plasma and replacing it with other fluids, a process called plasma exchange.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

considered by the Investigator to be free of signs and symptoms suggestive of any serious opportunistic infection
willing to discontinue and remain free from concomitant immunosuppressive or immunomodulatory treatment (including interferon beta and glatiramer acetate) for the duration of the study
willing and able to comply with the site's plasma exchange protocol which may require hospitalization or daily visits

Exclusion Criteria:

considered by the Investigator to be immunocompromised
history of, or available abnormal laboratory results indicative of any major disease that would preclude the administration of a recombinant humanized antibody immunomodulating agent for the duration of the study.
condition(s) considered to be contraindication(s) for plasma exchange, including but not limited to bleeding diathesis, hypotension, or vascular access limitations

Study is for people with:

Multiple Sclerosis

Phase:

Early Phase 1

Estimated Enrollment:

12

Study ID:

NCT00424788

Recruitment Status:

Completed

Sponsor:

Biogen

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There are 2 Locations for this study

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Cleveland Clinic Mellen Center for MS
Cleveland Ohio, 44195, United States
Center for Neurological Disorders, Aurora Health Care
Milwaukee Wisconsin, 53201, United States

How clear is this clinincal trial information?

Study is for people with:

Multiple Sclerosis

Phase:

Early Phase 1

Estimated Enrollment:

12

Study ID:

NCT00424788

Recruitment Status:

Completed

Sponsor:


Biogen

How clear is this clinincal trial information?

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