bluebird bio Announces Completion of its Q2 2024 Form 10-Q Filing

BLUE 09.27.2024

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  • 12.08.2024 - bluebird bio Presents Positive Long-Term Data On LYFGENIA™ (lovotobegligene autotemcel) Gene Therapy for Sickle Cell Disease at 66th American Society of Hematology (ASH) Annual Meeting and Exposition
  • 12.07.2024 - Long-Term Follow-Up Data Continue to Support Beti-Cel as a Potentially Curative Gene Therapy for β-Thalassemia Patients Who Require Regular Transfusions Through Achievement of Durable Transfusion Independence and Normal or Near-Normal Adult Hb Levels
  • 12.04.2024 - bluebird bio Announces 1-for-20 Reverse Stock Split

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  • 01.08.2025 - 4 Statement of changes in beneficial ownership of securities
  • 01.07.2025 - 144 Report of proposed sale of securities
  • 12.13.2024 - 8-K Current report

SOMERVILLE, Mass.--(BUSINESS WIRE)--Sep. 27, 2024--bluebird bio, Inc.(Nasdaq: BLUE) today announced that it has completed the filing of its Form 10-Q for the quarter endedJune 30, 2024(the “Q2 2024 Form 10-Q”) with theSecurities and Exchange Commission(“SEC”).

With the completion of this filing, the Company is now current in itsSECperiodic reporting obligations.

About bluebird bio, Inc.

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

Founded in 2010, bluebird has been setting the standard for gene therapy for more than a decade—first as a scientific pioneer and now as a commercial leader. bluebird has an unrivaled track record in bringing the promise of gene therapy out of clinical studies and into the real-world setting, having secured FDA approvals for three therapies in under two years. Today, we are proving and scaling the commercial model for gene therapy and delivering innovative solutions for access to patients, providers, and payers.

With a dedicated focus on severe genetic diseases, bluebird has the largest and deepest ex-vivo gene therapy data set in the field, with industry-leading programs for sickle cell disease, β-thalassemia and cerebral adrenoleukodystrophy. 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.

bluebird continues to forge new paths as a standalone commercial gene therapy company, 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.

View source version onbusinesswire.com:https://www.businesswire.com/news/home/20240927347484/en/

Investors:Courtney O’Leary, 978-621-7347coleary@bluebirdbio.com

Media:Jess Rowlands, 857-299-6103jess.rowlands@bluebirdbio.com

Source: bluebird bio, Inc.

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