Safety of Onasemnogene Abeparvovec for Patients With Spinal Muscular Atrophy 8.5 kg or Heavier in a Global Managed Access Program

Spinal muscular atrophy is a rare, neurodegenerative disorder caused by biallelic deletions in the survival motor neuron (SMN1) gene. Onasemnogene abeparvovec is a one-time, intravenous gene replacement therapy designed to deliver the SMN1 transgene. Although available in many geographies, it is not...

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Veröffentlicht in:Pediatric neurology 2022-07, Vol.132, p.27-32
Hauptverfasser: Chand, Deepa H., Mitchell, Susan, Sun, Rui, LaMarca, Nicole, Reyna, Sandra P., Sutter, Thao
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Sprache:eng
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Zusammenfassung:Spinal muscular atrophy is a rare, neurodegenerative disorder caused by biallelic deletions in the survival motor neuron (SMN1) gene. Onasemnogene abeparvovec is a one-time, intravenous gene replacement therapy designed to deliver the SMN1 transgene. Although available in many geographies, it is not approved globally. The Global Managed Access Program (GMAP) expanded treatment access to patients in countries where treatment was not approved. Previous onasemnogene abeparvovec clinical trials included patients with body weight
ISSN:0887-8994
1873-5150
DOI:10.1016/j.pediatrneurol.2022.05.001