MARKET

BLUE

BLUE

Bluebird Bio Inc
NASDAQ
1.220
+0.020
+1.67%
Opening 11:51 07/26 EDT
OPEN
1.240
PREV CLOSE
1.200
HIGH
1.250
LOW
1.170
VOLUME
1.35M
TURNOVER
0
52 WEEK HIGH
5.53
52 WEEK LOW
0.8450
MARKET CAP
235.15M
P/E (TTM)
-1.6385
1D
5D
1M
3M
1Y
5Y
1D
Actinium wins FDA nod to conduct clinical trial for radiotherapy
Healthcare Actinium wins FDA nod to conduct clinical trial for radiotherapy. Company's radiopharma candidate Iomab-ACT to be used as conditioning agent before bone marrow transplant in patients with sickle cell disease. The company will collaborate with Columbia University to conduct the study.
Seeking Alpha · 1d ago
Weekly Report: what happened at BLUE last week (0715-0719)?
Weekly Report · 4d ago
Weekly Report: what happened at BLUE last week (0708-0712)?
Weekly Report · 07/15 09:11
Bluebird Bio (BLUE) Gets a Buy from Bank of America Securities
TipRanks · 07/10 13:17
Vertex: Strategic Diversification From Gene Therapy To Acute Pain Management
Seeking Alpha · 07/09 16:31
Weekly Report: what happened at BLUE last week (0701-0705)?
Weekly Report · 07/08 09:11
bluebird bio Reports Inducement Grant to CFO James Sterling Under Nasdaq Listing Rule 5635(c)(4)
Bluebird bio, Inc. Granted stock options to its chief financial officer, James Sterling, to purchase 300,000 shares of common stock. The stock options vest over four years. Bluebird bio is pursuing curative gene therapies to give patients and their families more bluebird days.
Barchart · 07/03 15:05
Weekly Report: what happened at BLUE last week (0624-0628)?
Weekly Report · 07/01 09:11
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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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