Worries Mount Over Cancer Risks in Bluebird Bio's Gene Therapy [Yahoo! Finance]
bluebird bio, Inc. (BLUE)
Last bluebird bio, inc. earnings: 2/18 04:05 pm
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Source: Yahoo! Finance
Bio Inc's (NASDAQ: BLUE ) gene therapy for a severe neurological disorder in clinical trials have developed blood cancers. This marks an increase of four cases since June 2022, when the emergence of three cancer cases led the FDA to convene an advisory panel before approving the therapy, now marketed as Skysona. The STAT News report noted that one child passed away due to complications from cancer treatment. Researchers anticipate more cases of cancer could arise in the coming years and are conducting regular blood tests to monitor the patients. In September 2022, the FDA approved Bluebird Bio's Skysona, aka eli-cel, to slow the progression of neurologic dysfunction in boys 4-17 years of age with early, active cerebral adrenoleukodystrophy (CALD When in December 2023, the FDA approved Bluebird Bio's Lyfgenia (lovotibeglogene autotemcel (lovo-cel)) cell-based gene therapy for sickle cell disease, a black box warning was included in the label for Lyfgenia as hematologic malignan
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- bluebird bio Reports Third Quarter 2024 Results and Highlights Operational Progress and 2024 GuidanceBusiness Wire
- bluebird bio, Inc. (NASDAQ: BLUE) is now covered by analysts at StockNews.com. They set a "sell" rating on the stock.MarketBeat
- bluebird bio Adjourns Meeting of Stockholders and Announces Third Quarter Results CallBusiness Wire
- bluebird bio to Present Additional Long-Term Follow-up Data from Gene Therapy Programs in Sickle Cell Disease and Beta-Thalassemia at the 66th American Society of Hematology (ASH) Annual Meeting and ExpositionBusiness Wire
- bluebird bio, Inc. (NASDAQ: BLUE) is now covered by analysts at StockNews.com. They set a "sell" rating on the stock.MarketBeat
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- 11/14/24 - Beat
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