MARKET

BLUE

BLUE

Bluebird Bio Inc
NASDAQ
1.020
+0.067
+7.03%
After Hours: 1.020 0 0.00% 19:13 04/19 EDT
OPEN
0.9500
PREV CLOSE
0.9530
HIGH
1.030
LOW
0.9400
VOLUME
8.18M
TURNOVER
0
52 WEEK HIGH
5.53
52 WEEK LOW
0.8790
MARKET CAP
196.60M
P/E (TTM)
-1.3699
1D
5D
1M
3M
1Y
5Y
CRISPR Therapeutics Stock (NASDAQ:CRSP) Pushes Lower, But Fundamentals Are Intact
NASDAQ · 15h ago
BUZZ-bluebird delays filing of Q1 and 2023 reports, shares fall
Bluebird bio's shares fall 3% to 96 cents in extended trading. Gene therapy developer delays filing of Q1 and 2023 reports. Company says delays due to work required to restate financial statements. Company's stock down 70.8% in the past 12 months.
Reuters · 3d ago
Bluebird Bio Inc Anticipates It Will Be Delayed In Filing Its Quarterly Report On Form 10-Q For Q1 Of 2024
Benzinga · 3d ago
BLUEBIRD BIO INC - ANTICIPATES IT WILL BE DELAYED IN FILING ITS QUARTERLY REPORT ON FORM 10-Q FOR THE FIRST QUARTER OF 2024
Reuters · 3d ago
bluebird (BLUE) Underperforms Industry YTD Amid Challenges
NASDAQ · 3d ago
TD Cowen says sickle cell therapies may get higher CMS payments
Healthcare TD Cowen says sickle cell therapies may get higher CMS payments. Vertex/CRISPR’s Casgevy and bluebird bio's Lyfgenia were approved by the FDA for sicklecell disease in December. The two new therapies for the disease may get enhanced payments under proposed guidelines by CMS.
Seeking Alpha · 4d ago
Is Bluebird Bio Stock a Buy?
Bluebird Bio has three products on the market, but the company isn't profitable. Bluebird Bio's gene therapies are complex and expensive to manufacture and administer to patients. The company only has two programs, both of which are gene therapies for sickle cell disease. The small biotech's financial constraints may prevent it from truly taking off.
The Motley Fool · 5d ago
Weekly Report: what happened at BLUE last week (0408-0412)?
Weekly Report · 5d ago
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About BLUE
bluebird bio, Inc. is a biotechnology company. The Company is focused on researching, developing, and commercializing potentially curative gene therapies for severe genetic diseases based on its lentiviral vector (LVV) gene addition platform. Its lead gene therapy programs for sickle cell disease, B-thalassemia, and cerebral adrenoleukodystrophy and is advancing research to apply new technologies to these and other diseases. It has two gene therapies: ZYNTEGLO (betibeglogene autotemcel) and SKYSONA (elivaldogene autotemcel). ZYNTEGLO is the first gene therapy for people with B-thalassemia who require regular red blood cell transfusions. SKYSONA (elivaldogene autotemcel), also known as eli-cel, is used to slow the progression of eurologic dysfunction in boys 4-17 years of age with early, active cerebral adrenoleukodystrophy (CALD). It is also developing (lovotibeglogene autotemcel), also known as lovo-cel, as a one-time treatment for patients with sickle cell disease (SCD).

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