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Community Spotlight: Nicole Stickane Advocates for Newborn Screening in Texas

August 13, 2020
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In late July, the Texas Newborn Screening Advisory Committee held a meeting— virtually, of course —to hear an update on the status of statewide newborn screening for spinal muscular atrophy […]

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Genentech Releases Evrysdi™ FDA Approval Letter to the SMA Community

August 11, 2020
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Dear SMA Patient Advocacy Community, As part of our ongoing partnership and following your request to receive updates about the risdiplam clinical development program, we are delighted to share with […]

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Genentech Receives FDA Approval of Evrysdi (risdiplam) for the Treatment of SMA

August 7, 2020
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Genentech, a member of the Roche Group, today announced that it has received approval from the U.S. Food and Drug Administration (FDA) for Evrysdi (risdiplam) to treat adults and children 2 months and […]

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Cure SMA Launches New Medical Alert Bracelet Support Program

July 29, 2020
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Along with funding SMA research and care, Cure SMA provides thousands of individuals and families with vital support and resources that help people navigate life with spinal muscular atrophy (SMA). […]

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Cure SMA to Meet with FDA for Critical Path Innovation Meeting

July 28, 2020
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We are excited to share with the SMA community that the U.S. Food and Drug Administration (FDA) has granted Cure SMA a Critical Path Innovation Meeting (CPIM). This means that […]

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Biogen Plans to Initiate Phase 4 Study Evaluating Benefit of Spinraza in Patients Treated with Zolgensma

July 21, 2020
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Biogen Inc., today announced, it plans to initiate a global Phase 4 clinical study, RESPOND, to examine the clinical benefit and assess the safety of SPINRAZA (nusinersen) in infants and children with […]

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