An FDA decision on bluebird bio’s third gene therapy isn’t expected until December, but Novartis has already locked up a potential priority review voucher that might result.
Novartis agreed to purchase bluebird’s Rare Pediatric Disease PRV for $103 million, should the FDA grant one, bluebird announced Monday. Its gene therapy lovotibeglogene autotemcel (lovo-cel) is currently under FDA review for sickle cell disease in patients 12 years and older, with a decision anticipated by Dec. 20.
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