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Drug Review Europe Neurology

EU Crunch Time For Bluebird’s Neurodegenerative Disorder Gene Therapy

US Filing Expected Mid-2021

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Executive Summary

The EU could become the first market in which eli-cel is approved if the gene therapy for cerebral adrenoleukodystrophy this week passes muster with the European Medicines Agency.

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This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

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