5-year Evrysdi study confirms efficacy and safety for Type 1 SMA children, with 91% alive, 81% off ventilation, and 59% sitting without support.

5-year data from Roche's Evrysdi study confirms its efficacy and safety for children with Type 1 spinal muscular atrophy (SMA). At the end of Year 5, 91% of children were alive, 81% without permanent ventilation, and 59% could sit without support. Over 15,000 patients have been treated globally, with Evrysdi now approved in 100+ countries.

June 07, 2024
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