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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.

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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 Study CFTY720D2309

The purpose of this clinical research study is to find out if an oral once-a-day investigational drug called fingolimod is safe and has beneficial effects in people who have relapsing-remitting Multiple Sclerosis (MS) over a two year period. Fingolimod is an oral once-a-day medicine which has not been approved yet for the treatment of patients with multiple sclerosis and is therefore not “on the market” (available for you to buy) in any country. For more information on this study, please visit www.msclinicaltrials.com. Please note that by visiting this website, you are leaving Novartis. As a resource to our visitors, Novartis may provide links to other Web sites. We try to carefully choose websites that we believe are useful and meet our high standards. However, Novartis does not control, endorse, promote, or have any affiliation with any other website unless it is expressly stated. Novartis is not responsible for the content, accuracy, or any other aspect of the information contained on such linked sites
Trial phase: Phase 3
Participation Duration: 14 visits to the study center, over a period of 24 months.
Protocol Number: CFTY720D2309





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