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Thursday, 12/14/2023 7:37:15 AM

Thursday, December 14, 2023 7:37:15 AM

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Item 7.01
Regulation FD Disclosure.


Following the FDA approval of LYFGENIA on December 8, 2023 for sickle cell disease in patients 12 and older with a history of vaso-occlusive events, bluebird bio, Inc. (the “Company”) has signed an outcomes-based agreement with an organization representing approximately 100 million covered lives in the U.S. Additionally, the Company is in advanced discussions with a number of the nation’s other large commercial payers and more than 15 Medicaid agencies collectively representing 80% of individuals with sickle cell disease in the U.S. The Company anticipates 85 to 105 patient starts (cell collections) combined across all three of its commercial products (LYFGENIA, ZYNTEGLO, SKYSONA) in 2024.

Bluebird Bio Said Anticipates 85 To 105 Patient Starts Combined Across All Three Of Its Commercial Products In 2024…
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