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Spark Therapeutics (ONCE) Confirms FDA Advisory Committee Unanimously Recommended Approval of LUXTURNA for Patients with Biallelic RPE65-mediated IRD
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Spark Therapeutics Submits Marketing Authorization Application to European Medicines Agency for Investigational LUXTURNAâ„¢ (voretigene neparvovec)
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12,341 total articles have been posted to this entity.
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