bluebird bio, Inc.

BLUE

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Lead Plaintiff Deadline:
May 28, 2024

Days Left:
-48

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bluebird bio, Inc. Form












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Allegations

According to the complaint, on December 8, 2023, Blue announced that the Food and Drug Administration (FDA) approved its drug Lyfgenia (lovotibeglogene autotemcel), also known as lovo-cel for the treatment of sickle cell disease in patients ages 12 and older who have a history of vaso-occlusive events (VOEs). However, the Lyfgenia approval came with a black box warning for haematological malignancies after two patients developed AML during the clinical trials. Analysts noted that they did not expect the black box warning or the absence of a priority review voucher.Following this news, Blue’s stock price fell by $1.95 per share, or approximately 40% to close at $2.86 per share.

Eligibility

In order to be included in the lawsuit, you must have incurred a loss on shares of bluebird bio purchased or acquired during the class period listed above.

Lead Plaintiff Deadline

If you suffered a loss in bluebird bio during the relevant time frame, you have until May 28, 2024 to request that the Court appoint you as lead plaintiff. Your ability to share in any recovery doesn't require that you serve as a lead plaintiff.

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