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Five-year data from Genentech SMA study released

SMA patients in the long-term extension Evrysdi study maintained or improved key developmental skills over the five-year period, data shows.

United kingdomGiovanni baranelloLevi garrawayResearch clinical care meetingHead of global product developmentRoche groupInstitute of child health hospitalOrmond street instituteChild healthGreat ormond street hospitalChief medical officerGlobal productClinical care

Spinraza benefits SMA children not helped by Zolgensma: Interim data

Spinraza benefits SMA children not helped by Zolgensma: Interim data
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United statesMaha radhakrishnanNovarti zolgensmaWorld health organizationResearch clinical care meetingClinical care meetingPhiladelphia infant testNeuromuscular disordersHammersmith functional motor scale expandedRevised upper limbAlcyone therapeutics

Biogen Reports New Spinraza Data In Atrophy Patients After Incomplete Response To Novartis Treatment - Ionis Pharmaceuticals (NASDAQ:IONS), Biogen (NASDAQ:BIIB)

Biogen Inc (NASDAQ: BIIB) announced new Spinraza (nusinersen) data that were presented at the SMA Research & Clinical Care Meeting 

William blairIonis pharmaceuticals incResearch clinical care meetingClinical care meeting

Four-year follow up data for Roche s Evrysdi show continued

Data from ongoing FIREFISH study confirm long-term efficacy and safety profile of Evrysdi in children with Type 1 SMANinety-one percent of children were.

City ofUnited kingdomUnited statesLoren kalmKirti pandeyNathalie altermattLevi garrawayGiovanni baranelloRoche group media relationsDrug administrationEuropean medicines agencyOffice of orphan products developmentSociety for medicines researchInstitute of child health hospitalHead of global product developmentRoche group

Four-Year Follow-Up Data for Genentech s Evrysdi Show Continued Increase in Number of Children With a Severe Form of Spinal Muscular Atrophy (SMA) Able to Sit, Stand and Walk

– Data from ongoing FIREFISH study confirm long-term efficacy and safety profile of Evrysdi in children with Type 1 SMA – – Ninety-one percent of children were alive at month 48 – – More than 95% maintained the ability to swallow - without treatment they would have required feeding support and majority would have died within 2 years – – Evrysdi is now approved in 99 countries with more than 8,500 patients treated globally –

South san franciscoUnited statesCity ofUnited kingdomLevi garrawayGiovanni baranelloInstitute of child health hospitalSociety for medicines researchResearch clinical care meetingDrug administrationEuropean medicines agencyOffice of orphan products developmentRoche groupToddler development third editionGlobal product developmentBritish pharmacological society

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