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bluebird bio is pursuing curative gene therapies to give patients and their families more bluebird days.

With a dedicated focus on severe genetic diseases, bluebird has industry-leading programs for sickle cell disease, β-thalassemia and cerebral adrenoleukodystrophy and is advancing research to apply new technologies to these and other diseases. We custom design each of our therapies to address the underlying cause of disease and have developed in-depth and effective analytical methods to understand the safety of our lentiviral vector technologies and drive the field of gene therapy forward.

Founded in 2010, bluebird has the largest and deepest ex-vivo gene therapy data set in the world—setting the standard for the industry. Today, bluebird continues to forge new paths, combining our real-world experience with a deep commitment to patient communities and a people-centric culture that attracts and grows a diverse flock of dedicated birds.

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- Non-dilutive capital meaningfully strengthens Company’s financial position - SOMERVILLE, Mass. --(BUSINESS WIRE)--Nov. 30, 2022-- bluebird bio, Inc. (NASDAQ: BLUE) (“bluebird bio” or the “Company”) today announced that it has entered into a definitive agreement to sell a Rare Pediatric Disease

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- Commercial launch of ZYNTEGLO® ( betibeglogene autotemcel ) underway; on track for first apheresis in the fourth quarter of 2022 - - Chris Krawtschuk appointed chief financial officer - - Ended quarter with $186M in cash and cash equivalents, marketable securities and restricted cash -

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SOMERVILLE, Mass. --(BUSINESS WIRE)--Nov. 2, 2022-- bluebird bio, Inc. (NASDAQ: BLUE) today announced that members of the management team will participate in the 31 st Annual Credit Suisse Healthcare Conference , Tuesday, November 8 , at 5:00 p.m. PT at the Terranea Resort , Rancho Palos Verdes,

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