FDA approves Roche’s Evrysdi for use in babies under two months with spinal muscular atrophy (SMA)
The Pharma Data
MAY 31, 2022
About Evrysdi® (risdiplam) Evrysdi is a survival motor neuron 2 (SMN2) splicing modifier designed to treat SMA caused by mutations in chromosome 5q that lead to SMN protein deficiency. Evrysdi is now approved in the US to treat SMA in children and adults of all ages. Jude Children’s Research Hospital.
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