Expanded Access Program (EAP) to provide Nusinersen to Patients with Infantile-onset Spinal Muscular Atrophy (SMA)
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- STATUS
- Not Recruiting
Updated on 19 February 2024
Summary
The purpose of this study is to provide access to nusinersen to eligible patients with Infantile-onset Spinal Muscular Atrophy (SMA) in the US.
Description
The purpose of this study is to provide access to nusinersen to eligible patients with Infantile-onset Spinal Muscular Atrophy (SMA) in the US.
Details
| Condition | spinal muscular atrophy |
|---|---|
| Age | 100years or below |
| Clinical Study Identifier | TX7237 |
| Last Modified on | 19 February 2024 |
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