MS Awareness Month Raises Awareness of Individuals Living with Multiple Sclerosis

For the more than 400,000 Americans living with multiple sclerosis (MS), the support of loved ones, care partners and organizations such as the Multiple Sclerosis Association of America (MSAA) is crucial to improving quality of life. To help increase awareness of this disease, MSAA is taking part in observing March as MS Awareness Month.

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MSAA Wins 2015 Bronze Telly Award for Affordable Care Act Video

MSAA is proud to announce that its latest video, “What You Need To Know About The Affordable Care Act” was selected as a winner in the 36th Annual Telly Awards in the category of Health and Fitness! Winners of the Telly Awards represent the best work of the most respected advertising agencies, production companies, television stations, cable operators, and corporate video departments in the world.

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Multiple Sclerosis Coalition Endorses AAN Position Statement

The member organizations of the Multiple Sclerosis Coalition (MSC) unanimously endorsed the American Academy of Neurology’s (AAN) position statement entitled Availability of Disease Modifying Therapies (DMT) for Treatment of Relapsing Forms of Multiple Sclerosis.

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Swimming for Health and Wellness … and a Good Cause

Health experts tout swimming as one of the best all-around, total-body workouts. It builds both strength and cardiovascular endurance, and is well-suited for all ages and abilities.

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Multiple Sclerosis Coalition Backs Data-Gathering Bill

The Multiple Sclerosis Coalition’s (MSC) entire membership is providing support for bipartisan legislation to establish a data system to track the incidence and prevalence of neurological diseases, including multiple sclerosis. The bill, introduced in the U.S. House of Representatives by Congressmen Michael C. Burgess, M.D., (R-TX), and Chris Van Hollen (D-MD), could lead to a better understanding of the disease and provide new disease targets.

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Keep Your New Year’s Resolutions and Support a Good Cause

Exercising more often is a popular New Year’s resolution, but one that too often proves difficult to keep. But what if thousands of people living with multiple sclerosis (MS) were counting on you to keep that commitment?

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Changes Made to Tecfidera’s Label

The United States Food and Drug Administration (FDA) recently made some changes to the product labeling for Tecfidera® (dimethyl fumarate). These changes instruct physicians on how to best prescribe the drug for their patients to minimize the potential for certain side effects and adverse events. The revisions are described below; please note that several of the definitions given are from MedlinePlus (from the National Institutes of Health).

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PPMS Study Does Not Meet Primary Endpoint

On December 1, 2014, Novartis announced that their Phase III INFORMS trial with Gilenya® (fingolimod) for individuals with primary-progressive multiple sclerosis (PPMS) did not meet its primary endpoint. Presently, this disease-modifying therapy, taken orally (by mouth), is approved for the long-term treatment of relapsing forms of MS. The hope was that Gilenya would also prove effective in treating PPMS, a less-common form of MS that presently has no approved treatments available to slow disease activity.

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Lemtrada™ Receives FDA Approval for Relapsing Forms of MS

The United States Food and Drug Administration (FDA) announced today that Lemtrada™ (alemtuzumab) has been approved for the long-term treatment of relapsing forms of multiple sclerosis (MS). Given via intravenous (IV) infusion for a course of five days and followed one year later by a second three-day course, Lemtrada has been approved as a second-line therapy. This classification refers to a drug that may only be prescribed when other FDA-approved treatments fail or are not tolerated well by a patient. Lemtrada should generally be prescribed for patients who have had an inadequate response to two or more of the disease-modifying therapies, because of the medication’s safety profile.

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Phase III Study Data Added to Aubagio’s Labeling

Genzyme, a Sanofi company, has announced that the United States Food and Drug Administration (FDA) approved adding the data from two Phase III studies to Aubagio®’s (teriflunomide) product label. These studies are the TOWER and TOPIC studies, which provide additional study results for Aubagio’s efficacy and safety. Aubagio was approved by the FDA in September 2012 and was the second of three (to date) oral medications approved as a disease-modifying therapy (DMT) for relapsing forms of MS.

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