Non-Interventional, Postmarketing Surveillance Study of Nusinersen Sodium Injection

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• Hypersensitivity to the active substance or any of the excipients of nusinersen sodium injection.
• Current or past administration of nusinersen sodium injection, in either a commercial or a clinical study setting.

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• Other unspecified reasons that, in the opinion of the Investigator or the Sponsor, make the participant unsuitable for enrollment.
  • NOTE: Other protocol defined Inclusion/Exclusion criteria may apply.

• Ability of the participant or his/her legally authorized representative (e.g., parent or legal guardian), as appropriate and applicable, to understand the purpose and risks of the study and provide signed and dated informed consent and authorization to use protected health information in accordance with national and local subject privacy regulations.
• The decision to newly prescribe nusinersen sodium injection according to the local marketing authorization, including documentation of 5q SMA diagnosis, has been made by the Investigator and agreed to by the participant (or legally authorized representative)