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bluebird (BLUE) Q3 Loss Narrower Than Expected, Revenues Beat
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bluebird bio, Inc. (BLUE - Free Report) reported loss of $2.73 per share in the third quarter of 2018, narrower than the Zacks Consensus Estimate of loss of $2.88 but wider than the year-ago quarter’s loss of $1.73. The wider-than-expected year-over-year loss was due to higher research & development (R&D), and general & administrative (G&A) expenses on lower revenues.
Revenues of $11.5 million beat the Zacks Consensus Estimate of $8.3 million. Revenues were also up from $7.7 million recorded in the year-ago quarter.
bluebird’s stock has lost 28.3% in the year so far, wider than 15.6% decline registered by the industry.
Quarter in Detail
R&D expenses escalated to $116.7 million in the third quarter of 2018 from $61.5 million a year ago, driven by costs incurred from the advancement and expansion of the company’s pipeline.
G&A expenses of $44.5 million were up 93.5% in the year-ago quarter due to increases in employee-related costs as headcount increased to support overall growth.
In July 2018, bluebird raised approximately $600.6 million in net proceeds through a public equity offering. In August 2018, bluebird announced that Regeneron (REGN - Free Report) will make a $100-million investment in the company’s common stock at a price of $238.10 per share. The overall increase in cash, cash equivalents and marketable securities was offset by $40.0 million paid to Gritstone.
Pipeline Development
bluebird’s pipeline candidates for severe genetic diseases include LentiGlobin for the treatment of transfusion-dependent β-thalassemia (TDT) and severe sickle cell disease (SCD), and Lenti-D for the treatment of cerebral adrenoleukodystrophy (CALD). The oncology pipeline includes CAR T cell product candidates — bb2121 and bb21217 — for the treatment of multiple myeloma. The company is co-developing and co-promoting bb2121 in the United States with Celgene Corporation .
The pipeline progress in the third quarter was encouraging.
In the last month, bluebird announced that the European Medicines Agency (“EMA”) accepted the company’s marketing authorization application (MAA) for its investigational LentiGlobin gene therapy for the treatment of adolescents and adults, with transfusion-dependent β-thalassemia (TDT) and a non-β0/β0 genotype. We remind investors that LentiGlobin was previously granted an accelerated assessment by the Committee for Medicinal Products for Human Use (“CHMP”) of the EMA in July 2018, which, in turn, should reduce the EMA’s active review time of MAA from 210 days to 150 days.
Meanwhile, based on ongoing discussions with the FDA, bluebird bio is modifying and expanding its clinical development plans to explore efficacy endpoints that may allow the company to pursue a more accelerated development path in the United States for the treatment of patients with SCD, who have a history of vaso-occlusive events (VOEs).
In September 2018, bluebird announced updated results from phase II/III Starbeam study (ALD-102), evaluating its investigational Lenti-D gene therapy in boys aged 17 years or below with CALD. The company also announced initial results from the ongoing observational ALD-103 study of outcomes from allogeneic hematopoietic stem cell transplant (allo-HSCT) in boys aged 17 years or below with CALD. Meanwhile, bluebird entered a collaboration agreement with Gritstone Oncology, Inc. to research, develop and commercialize products for the treatment of cancer by using cell therapy.
Our Take
bluebird’s progress with its pipeline is encouraging. bluebird has an impressive pipeline of gene therapies for genetic diseases and cancer. LentiGlobin looks promising. We are also positive on the company’s collaboration with Regeneron as it provides the company with funds.
The company is also developing CAR T therapies in collaboration with Celgene for myeloma. The CAR T market holds potential and the successful development of the candidates will positively impact the company’s results. Celgene is expected to initiate a phase III study on bb2121 in third-line multiple myeloma shortly. Hence, we expect investors to focus on pipeline updates from the company.
Gilead’s earnings per share estimates increased from $6.58 to $6.87 for 2018 and from $6.47 to $6.75 for 2019 over the last thirty days.
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bluebird (BLUE) Q3 Loss Narrower Than Expected, Revenues Beat
bluebird bio, Inc. (BLUE - Free Report) reported loss of $2.73 per share in the third quarter of 2018, narrower than the Zacks Consensus Estimate of loss of $2.88 but wider than the year-ago quarter’s loss of $1.73. The wider-than-expected year-over-year loss was due to higher research & development (R&D), and general & administrative (G&A) expenses on lower revenues.
Revenues of $11.5 million beat the Zacks Consensus Estimate of $8.3 million. Revenues were also up from $7.7 million recorded in the year-ago quarter.
bluebird’s stock has lost 28.3% in the year so far, wider than 15.6% decline registered by the industry.
Quarter in Detail
R&D expenses escalated to $116.7 million in the third quarter of 2018 from $61.5 million a year ago, driven by costs incurred from the advancement and expansion of the company’s pipeline.
G&A expenses of $44.5 million were up 93.5% in the year-ago quarter due to increases in employee-related costs as headcount increased to support overall growth.
In July 2018, bluebird raised approximately $600.6 million in net proceeds through a public equity offering. In August 2018, bluebird announced that Regeneron (REGN - Free Report) will make a $100-million investment in the company’s common stock at a price of $238.10 per share. The overall increase in cash, cash equivalents and marketable securities was offset by $40.0 million paid to Gritstone.
Pipeline Development
bluebird’s pipeline candidates for severe genetic diseases include LentiGlobin for the treatment of transfusion-dependent β-thalassemia (TDT) and severe sickle cell disease (SCD), and Lenti-D for the treatment of cerebral adrenoleukodystrophy (CALD). The oncology pipeline includes CAR T cell product candidates — bb2121 and bb21217 — for the treatment of multiple myeloma. The company is co-developing and co-promoting bb2121 in the United States with Celgene Corporation .
The pipeline progress in the third quarter was encouraging.
In the last month, bluebird announced that the European Medicines Agency (“EMA”) accepted the company’s marketing authorization application (MAA) for its investigational LentiGlobin gene therapy for the treatment of adolescents and adults, with transfusion-dependent β-thalassemia (TDT) and a non-β0/β0 genotype. We remind investors that LentiGlobin was previously granted an accelerated assessment by the Committee for Medicinal Products for Human Use (“CHMP”) of the EMA in July 2018, which, in turn, should reduce the EMA’s active review time of MAA from 210 days to 150 days.
Meanwhile, based on ongoing discussions with the FDA, bluebird bio is modifying and expanding its clinical development plans to explore efficacy endpoints that may allow the company to pursue a more accelerated development path in the United States for the treatment of patients with SCD, who have a history of vaso-occlusive events (VOEs).
In September 2018, bluebird announced updated results from phase II/III Starbeam study (ALD-102), evaluating its investigational Lenti-D gene therapy in boys aged 17 years or below with CALD. The company also announced initial results from the ongoing observational ALD-103 study of outcomes from allogeneic hematopoietic stem cell transplant (allo-HSCT) in boys aged 17 years or below with CALD. Meanwhile, bluebird entered a collaboration agreement with Gritstone Oncology, Inc. to research, develop and commercialize products for the treatment of cancer by using cell therapy.
Our Take
bluebird’s progress with its pipeline is encouraging. bluebird has an impressive pipeline of gene therapies for genetic diseases and cancer. LentiGlobin looks promising. We are also positive on the company’s collaboration with Regeneron as it provides the company with funds.
The company is also developing CAR T therapies in collaboration with Celgene for myeloma. The CAR T market holds potential and the successful development of the candidates will positively impact the company’s results. Celgene is expected to initiate a phase III study on bb2121 in third-line multiple myeloma shortly. Hence, we expect investors to focus on pipeline updates from the company.
Zacks Rank
bluebird currently carries a Zacks Rank #4 (Sell). A better-ranked stock in the healthcare sector is Gilead Sciences, Inc. (GILD - Free Report) , which presently sports a Zacks Rank #1 (Strong Buy). You can see the complete list of today’s Zacks #1 Rank stocks here.
Gilead’s earnings per share estimates increased from $6.58 to $6.87 for 2018 and from $6.47 to $6.75 for 2019 over the last thirty days.
Today's Stocks from Zacks' Hottest Strategies
It's hard to believe, even for us at Zacks. But while the market gained +21.9% in 2017, our top stock-picking screens have returned +115.0%, +109.3%, +104.9%, +98.6%, and +67.1%.
And this outperformance has not just been a recent phenomenon. Over the years it has been remarkably consistent. From 2000 - 2017, the composite yearly average gain for these strategies has beaten the market more than 19X over. Maybe even more remarkable is the fact that we're willing to share their latest stocks with you without cost or obligation.
See Them Free>>