bluebird bio Reports Fourth Quarter and Full Year 2020 Financial Results and Highlights Operational Progress
bluebird bio reported its financial results for Q4 and full year 2020, noting a significant revenue increase from $44.7 million in 2019 to $250.7 million in 2020. Despite a net loss reduction to $618.7 million from $789.6 million, the company faces challenges, including a clinical hold on LentiGlobin studies due to safety events. Upcoming milestones include the PDUFA action date for ide-cel on March 27, 2021, and potential EU approval for eli-cel mid-year. The company is separating its severe genetic disease and oncology ventures by the end of 2021.
- Total revenues increased from $44.7 million in 2019 to $250.7 million in 2020, primarily driven by BMS collaboration and licensing revenue.
- Net loss reduced from $789.6 million in 2019 to $618.7 million in 2020, indicating improved financial management.
- First commercial infusion of ZYNTEGLO in Germany completed, marking a significant milestone.
- Successful presentation of favorable data at the ASH Annual Meeting showcasing the efficacy of LentiGlobin and ide-cel.
- Clinical hold imposed by the FDA on LentiGlobin studies due to serious adverse reactions, impacting ongoing research.
- Temporary suspension of ZYNTEGLO marketing in Europe due to the clinical hold and safety event investigations.
- Delays in regulatory submissions for β-thalassemia and CALD contingent on resolution of safety concerns.
bluebird bio, Inc. (NASDAQ:BLUE) today reported financial results and business highlights for the fourth quarter and full year ended December 31, 2020 and shared recent operational progress.
“For over ten years, bluebird bio has been pioneering gene therapies for patients with rare diseases and cancer, and our work continues with the analysis of the recent safety events identified in our HGB-206 study in patients with sickle cell disease. We have seen the transformative benefit of these therapies and are conducting a scientific and medical investigation to best inform our path forward on behalf of the patients we hope to serve with LentiGlobin,” said Nick Leschly, chief bluebird. “While this work is ongoing, we remain focused on the upcoming PDUFA action due date for ide-cel for multiple myeloma next month, the potential EU approval of eli-cel for CALD mid-year and the planned US filings for β-thalassemia and CALD later in the year. Through these challenges, we are keeping patients at the center and were very excited to reach a major milestone of the first commercial infusion of ZYNTEGLO in Germany earlier this month.”
RECENT HIGHLIGHTS
COMPANY
- CLINICAL HOLD OF PHASE 1/2 AND PHASE 3 STUDIES OF LENTIGLOBIN GENE THERAPY FOR SICKLE CELL DISEASE AND TEMPORARY SUSPENSION OF MARKETING OF ZYNTEGLO IN EUROPE – On February 16, 2021, bluebird bio announced that due to a Suspected Unexpected Serious Adverse Reaction (SUSAR) of acute myeloid leukemia and a SUSAR of myelodysplastic syndrome in our HGB-206 clinical study, the FDA has placed our clinical studies of LentiGlobin for SCD on clinical hold. We are investigating these events and plan to continue to work closely with the FDA in their review of these events. In addition, we are also engaged with the EMA in discussions regarding our proposed development plans for LentiGlobin for SCD in Europe. In light of these SUSARs, we have temporarily suspended marketing of ZYNTEGLO in Europe. Additionally, the EMA has paused the renewal procedure for ZYNTEGLO's conditional marketing authorization while the EMA's pharmacovigilance risk assessment committee reviews the risk-benefit assessment for ZYNTEGLO and determines whether any additional pharmacovigilance measures are necessary.
-
INTENT TO SEPARATE – On January 11, 2021, bluebird bio announced its intent to separate its severe genetic disease and oncology businesses into two independent, publicly traded companies (bluebird bio and “Oncology Newco”). The separation is expected to be completed by year-end 2021 and it is anticipated that the spin out of Oncology Newco is to be tax-free to shareholders, subject to receipt of a favorable Internal Revenue Service (IRS) ruling.
- Following the separation, bluebird bio intends to focus on delivery of its Core 3 therapies in β-thalassemia, cerebral adrenoleukodystrophy and sickle cell disease, expand access and reimbursement for our commercial product, ZYNTEGLO, in Europe and continue to explore innovative tools and technologies to ultimately bring these transformative medicines to more patients.
- Following the separation, Oncology Newco plans to support commercial success of ide-cel and continued development of bb21217, deliver on the oncology pipeline of cellular therapies with a focus on non-Hodgkin’s lymphoma, acute myeloid leukemia, next-generation multiple myeloma and solid tumors and advance next generation product cycling engine with an overarching goal of 1-2 investigational new drugs (INDs) in each of the years 2021 and 2022.
- At the time of separation, bluebird bio plans to capitalize each business with sufficient capital to achieve value creating milestones and intends to provide additional financial details closer to the date of separation.
TRANSFUSION DEPENDENT β-THALASSEMIA
- FIRST PATIENT TREATED WITH ZYNTEGLO GENE THERAPY - bluebird bio is announcing today that a patient was treated earlier this month with the first commercial infusion of ZYNTEGLO [betibeglogene autotemcel (beti-cel)]. The patient was treated at a Qualified Treatment Center (QTC) in Germany.
- TDT DATA AT ASH – On December 5, 2020, bluebird bio presented new data showing that all patients that achieved transfusion independence continue to remain free from transfusions up to six years in the ongoing long-term follow-up study (LTF-303) of beti-cel gene therapy in patients with TDT at the 62nd American Society of Hematology (ASH) Annual Meeting. The company also presented updated efficacy and safety results for pediatric patients in the Phase 3 HGB-207 (Northstar-2) and HGB-212 (Northstar-3) studies.
SICKLE CELL DISEASE
- FIRST PATIENT TREATED IN CONFIRMATORY HGB-210 STUDY –bluebird bio is announcing today that within the first quarter, the first patient was infused in HGB-210, a Phase 3 confirmatory study of LentiGlobin™ gene therapy (bb1111) for adults and pediatric subjects ≥2 and ≤50 years of age with sickle cell disease (SCD).
- SCD DATA AT ASH - On December 7, 2020, bluebird bio presented new data showing a complete elimination of severe vaso-occlusive events (VOEs) through 24 months of follow-up in patients who had a history of at least four severe VOEs and at least six months follow-up in Group C of its ongoing Phase 1/2 HGB-206 study of bb1111 for patients with SCD at the 62nd ASH Annual Meeting.
- MAGENTA COLLABORATION – On December 4, 2020, bluebird bio and Magenta Therapeutics announced an exclusive clinical trial collaboration to evaluate the utility of MGTA-145, in combination with plerixafor, for mobilization and collection of stem cells in patients with SCD. The combination approach has the potential to achieve safe, rapid and reliable mobilization of sufficient quantities of high-quality stem cells to ultimately improve outcomes associated with stem cell transplantation. The companies will co-fund the clinical trial and Magenta will retain all rights to its product candidate.
MULTIPLE MYELOMA
- CRB-401 DATA AT ASH – On December 5, 2020, bluebird bio and Bristol-Myers Squibb presented longer-term results showing ongoing deep and durable responses in the original Phase 1 study (CRB-401) of the companies’ investigational B-cell maturation antigen (BCMA) directed chimeric antigen receptor (CAR) T cell therapy, idecabtagene vicleucel (ide-cel), in patients with relapsed and refractory multiple myeloma at the 62nd ASH Annual Meeting.
- BB21217 DATA AT ASH - On December 5, 2020, bluebird bio and Bristol-Myers Squibb presented updated safety and efficacy results showing promising response rates and durability from the ongoing Phase 1 study (CRB-402) of bb21217, an investigational BCMA-directed CAR T cell therapy in patients with relapsed and refractory multiple myeloma at the 62nd ASH Annual Meeting. The company announced the study has completed enrollment and follow-up is ongoing as data continue to mature and the durability of response at the recommended phase 2 dose is assessed.
UPCOMING ANTICIPATED MILESTONES
Regulatory Outlook
- Multiple Myeloma: The FDA has set a Prescription Drug User Fee Act (PDUFA) goal date of March 27, 2021 for the approval of ide-cel (bb2121) in patients with relapsed and refractory multiple myeloma.
- SCD: The company is investigating the recently-reported safety events and plans to continue to work closely with the FDA in their review of these events to provide an update on the Company’s development plan and timeline for submission for regulatory approval.
- TDT: The company is on track to complete its rolling BLA submission to the U.S. FDA for beti-cel in mid-2021, contingent upon successful resolution of any U.S. FDA concerns applicable to the program arising out of the recently-reported safety events in the SCD program. This submission is anticipated to include patients with transfusion dependent β-thalassemia across all genotypes (including non-β0/β0 genotypes and β0/β0 genotypes).
- CALD: The company is on track to complete its BLA submission to the U.S. FDA for elivaldogene autotemcel (eli-cel) in mid-2021. The company plans to receive European approval for eli-cel in patients with cerebral adrenoleukodystrophy (CALD) in mid-2021.
Clinical Updates and Milestones
- Updated data from ongoing clinical study in patients with SCD by the end of 2021.
- Updated data from ongoing clinical studies in patients with TDT in mid-2021.
- Updated data from ongoing clinical studies in patients with CALD in mid-2021.
- bb21217 clinical data from the ongoing CRB-402 study in patients with multiple myeloma by the end of 2021.
- Submission of 1 - 2 investigational new drug (IND) applications by the end of 2021.
FOURTH QUARTER AND FULL YEAR 2020 FINANCIAL RESULTS
-
Cash Position: Cash, cash equivalents and marketable securities as of December 31, 2020 and December 31, 2019 were
$1.27 billion and$1.24 billion , respectively. The increase in cash, cash equivalents and marketable securities is primarily a result of proceeds received from the May 2020 public offering of the Company’s common stock and a one-time upfront payment received in connection with the Company’s amended collaboration with BMS, partially offset by cash used in support of ordinary course operating and commercial-readiness activities. -
Revenues: Total revenues were
$10.7 million for the three months ended December 31, 2020 compared to$10.0 million for the three months ended December 31, 2019. Total revenues were$250.7 million for the twelve months ended December 31, 2020 compared to$44.7 million for the twelve months ended December 31, 2019. The increase for the three-month period was primarily driven by an increase in royalty and other revenue. The increase for the twelve-month period was primarily driven by the amended BMS collaboration and monetization for ex-U.S. milestones and royalties from ide-cel and bb21217, with the majority of the revenue recognized relating to ide-cel license and manufacturing services. -
R&D Expenses: Research and development expenses were
$137.1 million for the three months ended December 31, 2020 compared to$161.8 million for the three months ended December 31, 2019. Research and development expenses were$588.0 million for the twelve months ended December 31, 2020 compared to$582.4 million for the twelve months ended December 31, 2019. The decrease for the three-month period was primarily driven by a decrease in manufacturing costs, partially offset by increased costs incurred through the amended BMS collaboration. The increase for the twelve-month period was primarily driven by an overall increase in costs incurred to advance and expand the company’s pipeline, partially offset by a decrease in manufacturing costs. -
SG&A Expenses: Selling, general and administrative expenses were
$77.0 million for the three months ended December 31, 2020 compared to$76.2 million for the three months ended December 31, 2019. Selling, general and administrative expenses were$286.9 million for the twelve months ended December 31, 2020 compared to$271.4 million for the twelve months ended December 31, 2019. The increase for both periods was largely attributable to increased headcount and costs incurred to support the Company’s ongoing operations and growth of its pipeline, partially offset by a decrease in costs related to commercial readiness activities due to delays during 2020 as a result of the COVID-19 pandemic. -
Net Loss: Net loss was
$199.9 million for the three months ended December 31, 2020 compared to$223.3 million for the three months ended December 31, 2019. Net loss was$618.7 million for the twelve months ended December 31, 2020 compared to$789.6 million for the twelve months ended December 31, 2019.
About bluebird bio, Inc.
bluebird bio is pioneering gene therapy with purpose. From our Cambridge, Mass., headquarters, we’re developing gene and cell therapies for severe genetic diseases and cancer, with the goal that people facing potentially fatal conditions with limited treatment options can live their lives fully. Beyond our labs, we’re working to positively disrupt the healthcare system to create access, transparency and education so that gene therapy can become available to all those who can benefit.
bluebird bio is a human company powered by human stories. We’re putting our care and expertise to work across a spectrum of disorders: cerebral adrenoleukodystrophy, sickle cell disease, β-thalassemia and multiple myeloma, using gene and cell therapy technologies including gene addition, and (megaTAL-enabled) gene editing.
bluebird bio has additional nests in Seattle, Wash.; Durham, N.C.; and Zug, Switzerland. For more information, visit bluebirdbio.com.
Follow bluebird bio on social media: @bluebirdbio, LinkedIn, Instagram and YouTube.
ZYNTEGLO, LentiGlobin, and bluebird bio are trademarks of bluebird bio, Inc.
Forward-Looking Statements
This release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995, including statements regarding the company’s financial condition, results of operations, as well as statements regarding the Company’s timing and expectations regarding its investigation of the relationship of the safety events in HGB-206 to the use of lentiviral vector BB305 in LentiGlobin gene therapy for SCD, and any myeloablation regimen used in connection with treatment; the plans for regulatory submissions for beti-cel (marketed as ZYTENGLO in the European Union), eli-cel, ide-cel, and LentiGlobin for SCD, including anticipated endpoints to support regulatory submissions and timing expectations; the company’s expectations regarding the potential for the suspension-based manufacturing process for lentiviral vector; the company’s expectations and execution under its revised operating plan, including its cash runway; its expectations for commercialization efforts for ZYNTEGLO in Europe; and the company’s expectations for the amended collaboration agreement with BMS; as well as the company’s intentions regarding the timing for providing further updates on the development and commercialization of ZYNTEGLO and the company’s product candidates; the timing, leadership, structure, including the division of assets among bluebird bio and Oncology Newco, and the impact of a separation; as well as the company’s intention to provide further updates on the separation and the related financing strategies for bluebird bio and Oncology Newco; and the tax free nature of the separation. Any forward-looking statements are based on management’s current expectations of future events and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements. These risks and uncertainties include, but are not limited to, the risk that the Company may not be able to definitively determine whether the lentiviral vector BB305 used in LentiGlobin gene therapy for SCD and in beti-cel is related to the safety events in a timely manner, or at all; the risk that the lentiviral vector BB305 has caused insertional oncogenic events, including acute myeloid leukemia; the risk that insertional oncogenic events associated with lentiviral vector or additional safety events associated with myeloablation will be discovered or reported over time; the risk that we may not be able to address regulatory authorities’ concerns quickly or at all and may not be able to resume our HGB-206 or HGB-210 studies in a timely manner, or at all; the risk that we may not resume patient treatment with ZYNTEGLO in the commercial context in a timely manner or at all; the risk that our lentiviral vector platform across our severe genetic disease programs may be implicated, affecting the development and potential approval elivaldogene autotemcel; the risks that we may not complete the separation on the terms or timeline currently contemplated if at all, achieve the expected benefits of a separation, and a separation could harm our business, results of operations and financial condition; the risk that the transaction might not be tax-free; we may be unable to make, on a timely or cost-effective basis, the changes necessary to operate as independent companies; Oncology Newco's lack of independent operating history and the risk that its accounting and other management systems may not be prepared to meet the financial reporting and other requirements of operating as an independent public company; dedicated financial and/or strategic funding sources may not be available on favorable terms; a separation or announcement thereof may adversely impact our ability to attract or retain key personnel; a separation may adversely impact the effectiveness of development and commercialization efforts by us and our partners; our businesses may be disrupted as a result of the announcement or pendency of the separation; the COVID-19 pandemic and resulting economic conditions will have a greater impact on the company’s operations and plans than anticipated; that our amended collaboration with BMS will not continue or be successful; that preliminary positive efficacy and safety results from our prior and ongoing clinical trials will not continue or be repeated in our ongoing or future clinical trials; the risk that our plans for submitting a BLA for LentiGlobin for SCD may be delayed if the FDA does not accept our comparability plans for the use of the suspension-based manufacturing process for LVV; the risk that the BLA for ide-cel is approved by the FDA in the timeline we expect, or at all; the risk of cessation or delay of any of the ongoing development activities, including clinical studies, and commercialization efforts due to delays from the COVID-19 pandemic’s impact on healthcare systems; the risk that the current or planned clinical trials of our product candidates will be insufficient to support regulatory submissions or marketing approval in the United States and European Union; the risk that regulatory authorities will require additional information regarding our product candidates, resulting in delay to our anticipated timelines for regulatory submissions, including our applications for marketing approval; the risk that we will encounter challenges in the commercial launch of ZYNTEGLO in the European Union, including in managing our complex supply chain for the delivery of drug product, or in obtaining sufficient coverage or reimbursement for our products; and the risk that any one or more of our product candidates, will not be successfully developed, approved or commercialized. For a discussion of other risks and uncertainties, and other important factors, any of which could cause our actual results to differ from those contained in the forward-looking statements, see the section entitled “Risk Factors” in our most recent Form 10-K, as well as discussions of potential risks, uncertainties, and other important factors in our subsequent filings with the Securities and Exchange Commission. All information in this press release is as of the date of the release, and bluebird bio undertakes no duty to update this information unless required by law.
bluebird bio, Inc. |
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Condensed Consolidated Statements of Operations |
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(in thousands, except per share data) |
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(unaudited) |
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For the three months ended
|
For the twelve months ended
|
||||||||||||||
|
2020 |
2019 |
2020 |
2019 |
||||||||||||
Revenue: |
|
|
|
|
||||||||||||
Service revenue |
$ |
5,522 |
|
$ |
5,827 |
|
$ |
114,064 |
|
$ |
30,729 |
|
||||
Collaborative arrangement revenue |
1,196 |
|
1,332 |
|
115,594 |
|
5,740 |
|
||||||||
Royalty and other revenue |
3,990 |
|
2,838 |
|
21,076 |
|
8,205 |
|
||||||||
Total revenues |
10,708 |
|
9,997 |
|
250,734 |
|
44,674 |
|
||||||||
Operating expenses: |
|
|
|
|
||||||||||||
Research and development |
137,094 |
|
161,821 |
|
587,956 |
|
582,413 |
|
||||||||
Selling, general and administrative |
76,974 |
|
76,202 |
|
286,896 |
|
271,362 |
|
||||||||
Cost of royalty and other revenue |
1,499 |
|
1,073 |
|
5,396 |
|
2,978 |
|
||||||||
Change in fair value of contingent consideration |
(877 |
) |
1,435 |
|
(6,468 |
) |
2,747 |
|
||||||||
Total operating expenses |
214,690 |
|
240,531 |
|
873,780 |
|
859,500 |
|
||||||||
Loss from operations |
(203,982 |
) |
(230,534 |
) |
(623,046 |
) |
(814,826 |
) |
||||||||
Interest income, net |
1,281 |
|
6,855 |
|
11,539 |
|
34,761 |
|
||||||||
Other income (expense), net |
3,080 |
|
535 |
|
(6,502 |
) |
(10,088 |
) |
||||||||
Loss before income taxes |
(199,621 |
) |
(223,144 |
) |
(618,009 |
) |
(790,153 |
) |
||||||||
Income tax (expense) benefit |
(253 |
) |
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FAQ
What were bluebird bio's total revenues for 2020?
bluebird bio reported total revenues of $250.7 million for the full year 2020.
What is the status of bluebird bio's LentiGlobin studies?
The FDA has placed a clinical hold on LentiGlobin studies due to serious safety events.
When is the PDUFA date for ide-cel?
The PDUFA action date for ide-cel is set for March 27, 2021.
What impact did bluebird bio's separation plan have on its business?
bluebird bio plans to separate its severe genetic disease and oncology businesses by the end of 2021, allowing a focused strategy for both sectors.
What steps is bluebird bio taking following the ZYNTEGLO suspension?
The company is engaged with the EMA and FDA to review safety events and continues to monitor the situation closely.
bluebird bio, Inc.
NASDAQ:BLUEBLUE RankingsBLUE Latest NewsBLUE Stock Data
89.74M
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0.63%
43.69%
24.6%
Biotechnology
Biological Products, (no Disgnostic Substances)
United States of America
SOMERVILLE
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