Effect of Tysabri in Patients With Relapsing-Remitting Multiple Sclerosis: A Follow-up Magnetization Transfer Imaging (MTI) Study

Completed

Conditions studied: Multiple Sclerosis

In brief

The primary objective of this study is to define the effect of Tysabri in patients with relapsing-remitting (RR) multiple sclerosis (MS) over 2 years. The investigators will also explore the extent of remyelination in MS patients treated with Tysabri over 2 years. A secondary objective of this study is to investigate differences in the capacity for remyelination between patients who do or do not respond to Tysabri monotherapy during the same 24 months. A tertiary objective of this study is to monitor Tysabri effect in MS antiphospholipid antibodies positive and MS antiphospholipid antibodies negative patients and to determine perfusion differences according to the antiphospholipid antibodies positivity status.

Key facts

Study ID: NCT00937677
Run by: University at Buffalo
People needed: 85
Starts: 2007-11-01
Expected to finish: 2010-11-01
Last updated by the study team: 2011-09-07

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

Patient diagnosed with clinically definite MS according to the Polman criteria
Age 18-65
Have a RR disease course
Have EDSS scores less than or equal to 5.5 {Kurtzke, 1983 #15}
Have disease duration less than 20 years
Fulfilled the TOUCH enrollment requirements and started on Tysabri monotherapy
Signed informed consent
None of the exclusion criteria

You may not qualify if…

Primary progressive, secondary progressive, or progressive relapsing MS. Primary progressive, secondary progressive or progressive relapsing multiple sclerosis.
A clinically significant infectious illness (e.g., cellulitis, abscess, pneumonia, septicemia) within 30 days prior to drug start.
History of, or abnormal laboratory results indicative of, any significant cardiac, endocrinologic, hematologic, hepatic, immunologic, metabolic, urologic, pulmonary, gastrointestinal, dermatologic, psychiatric, renal, and/or other major disease that, in the opinion of the investigator, would preclude the administration of natalizumab for the duration of the study.
History of severe allergic or anaphylactic reactions or known drug hypersensitivity.
Abnormal blood tests, performed at the screening visit, which exceed any of the limits defined below:
ALT/ SGPT, or AST/ SGOT > three times the upper limit of normal (i.e., 3xULN).
Total white blood cell (WBC) count <2,300/mm3.
Platelet count <100,000/mm3.
Creatinine > 2xULN.
Prothrombin time (PT) > ULN.
Any prior treatment during the 2 weeks prior to study screening with agents such as IFN-β, GA, IVIG, or on the following immunosuppressant therapies for less than 3 months: mitoxantrone, cyclophosphamide, cladribine, fludarabine, cyclosporine, azathioprine, methotrexate, Cellcept, etc.
History of alcohol or drug abuse within 2 years prior to randomization.
Female subjects who are not postmenopausal for at least 1 year, surgically sterile, or willing to practice effective contraception (as defined by the investigator) during the study. The rhythm method is not to be used as the sole method of contraception.
Nursing mothers, pregnant women, and women planning to become pregnant while on study.
Unwillingness or inability to comply with the requirements of this protocol including the presence of any condition (physical, mental, or social) that is likely to affect the subject's ability to comply with the study protocol.
Any other reasons that, in the opinion of the Investigator, indicate that the subject is unsuitable for enrollment into this study.

Where it is running

Jacobs Neurological Institute — Buffalo, New York, United States

Full record on ClinicalTrials.gov

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