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USFDA panel backs Bluebird bio gene therapy for blood disorder
![USFDA panel backs Bluebird bio gene therapy for blood disorder USFDA panel backs Bluebird bio gene therapy for blood disorder](https://medicaldialogues.in/h-upload/2020/04/16/750x450_127346-124898-usfda.webp)
The FDA is expected to decide on beti-cel's fate by Aug. 19 and eli-cel's by Sept. 16. The agency is not required to follow its advisers' recommendation, although it usually does.
New Delhi: Bluebird bio's treatment for a rare blood disorder received backing from advisers to the U.S. Food and Drug Administration on Friday, in a vote of confidence in gene therapies and bolstering the company beset by regulatory setbacks.
Read also: Moderna coronavirus vaccine effective for kids under five years: USFDA
Ruchika Sharma joined Medical Dialogue as an Desk Editor for the Business Section in 2019. She covers all the updates in the Pharmaceutical field, Policy, Insurance, Business Healthcare, Medical News, Health News, Pharma News, Healthcare and Investment. She has completed her B.Com from Delhi University and then pursued postgraduation in M.Com. She can be contacted at editorial@medicaldialogues.in Contact no. 011-43720751