US Food and Drug Administration. FDA approves first drug for spinal muscular atrophy
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US FDA approves Biogen’s SPINRAZA™ (nusinersen)
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Biogen. Biogen and Ionis Pharmaceuticals announce SPINRAZA (nusinersen) meets primary endpoint at interim analysis of phase 3 CHERISH study in later-onset spinal muscular atrophy
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US FDA Center for Drug Evaluation and Research. Medical review(s)
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Treatment of infantile-onset spinal muscular atrophy with nusinersen: a phase 2, open-label, dose-escalation study
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Biogen. Biogen and Ionis Pharmaceuticals report nusinersen meets primary endpoint at interim analysis of phase 3 ENDEAR study in infantile-onset spinal muscular atrophy
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Biogen. New data presented at World Muscle Society Congress support potential benefit of investigational treatment nusinersen in spinal muscular atrophy
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