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Novartis Clinical Trials and Medical Research Studies Recruiting in the U.S.

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Novartis Clinical Trials provides information about research studies recruiting within the U.S.

Visit ClinicalTrials.gov, a registry of federally and privately supported clinical trial for more information regarding clinical trials outside of the U.S.

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Multiple Sclerosis (MS)

An unpredictable disease of the central nervous system, multiple sclerosis (MS) can range from relatively benign to somewhat disabling to devastating, as communication between the brain and other parts of the body is disrupted. Many investigators believe MS to be an autoimmune disease -- one in which the body, through its immune system, launches a defensive attack against its own tissues. In the case of MS, it is the nerve-insulating myelin that comes under assault. Such assaults may be linked to an unknown environmental trigger, perhaps a virus. [Source: www.ninds.nih.gov]

Novartis is seeking people to participate in a clinical trial(s) testing the safety and effectiveness of Novartis products. Novartis recommends that you consult your doctor before participating in a clinical trial.

For more information about clinical trial participation, click here. Also, for additional information about how Novartis helps to protect the privacy of the personal information that you provide to us, please see the Novartis Privacy Policy.

Please review the details of the clinical trial(s) listed below and click on the one that you feel best suits your (or the participant's) condition.

Multiple Sclerosis (Primary Progressive) Study - D2306

The main purpose of this study is to evaluate how effective a Novartis investigational drug is in delaying disability progression in patients with primary progressive multiple sclerosis. It will also evaluate how safe and well tolerated the investigational drug is in patients with primary progressive multiple sclerosis.
Trial phase: Phase 3
Participation Duration: Study may last up to 5 years. During the first 3-years of the study there are up to 18 scheduled hospital/clinic visits: before starting study drug there will be 2 pre-treatment visits.
Protocol Number: CFTY720D2306






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