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Cure SMA Meets in Utah with State and Federal Elected Officials to Support Newborn Screening

October 13, 2017
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On Tuesday, Cure SMA staff members and family advocates, and clinicians from the University of Utah, met with Senator Orrin Hatch (R-UT) to discuss newborn screening for spinal muscular atrophy. […]

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Genentech/Roche Releases Clinical Trial Update for SUNFISH (RG7916)

October 12, 2017
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Genentech/Roche has provided the below community statement with clinical trial updates for SUNFISH (Type 2/3). The first patient is now enrolled in SUNFISH, as the trial advances to part two, […]

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Recording of the September Webinar on Spinraza Updates Now Available

September 29, 2017
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A recording of last week’s webinar updating the community on Spinraza access and administration sites is now available online. A PDF of the webinar presentation is also available for download. An update […]

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AveXis Announces Plan to Initiate Pivotal Trial of AVXS-101 in SMA Type 1 Using Product from New GMP Commercial Process

September 29, 2017
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AveXis, Inc., a clinical-stage gene therapy company developing treatments for patients suffering from rare and life-threatening neurological genetic diseases, today announced the U.S. Food and Drug Administration (FDA) has notified […]

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Cure SMA Contributes Article to a Special Issue of the Journal Gene Therapy

September 28, 2017
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To celebrate the FDA approval of Spinraza, Cure SMA contributed an article to the September special issue of the journal Gene Therapy. The issue , “Spinraza and Advanced Therapies: a […]

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Newborn Screening Advocacy Update

September 20, 2017
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At our Annual SMA Conference in July, we announced a grassroots campaign to implement newborn screening for SMA in all 50 states. We know that newborn screening and early treatment […]

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