Investors & Media

press releases

Date Title Teaser
08/09/17
Summary Togglebluebird bio to Present at Wedbush PacGrow Healthcare Conference CAMBRIDGE, Mass. --(BUSINESS WIRE)--Aug. 9, 2017-- bluebird bio, Inc. ( Nasdaq: BLUE ), a clinical-stage company committed to developing potentially transformative gene therapies for severe genetic diseases and T cell-based immunotherapies for cancer, today announced that members of the management
08/02/17
Summary Togglebluebird bio Reports Second Quarter 2017 Financial Results and Recent Operational Progress – Completed enrollment in Northstar -2, Phase 3 study of LentiGlobin TM drug product in patients with transfusion-dependent β-thalassemia (TDT) and non-β 0 /β 0 genotypes – – Presented updated clinical results from studies in relapsed/refractory multiple myeloma, TDT and severe sickle cell disease
06/27/17
Summary Togglebluebird bio Announces Pricing of Public Offering of Common Stock CAMBRIDGE, Mass. --(BUSINESS WIRE)--Jun. 27, 2017-- bluebird bio, Inc. (Nasdaq: BLUE), a clinical-stage biotechnology company committed to developing potentially transformative gene therapies for severe genetic diseases and cancer, today announced the pricing of an underwritten public offering of
06/26/17
Summary Togglebluebird bio Announces Topline Interim Clinical Data from Starbeam Study of Lenti-D™ Drug Product in Cerebral Adrenoleukodystrophy (CALD) – 15/17 patients (88%) in initial study cohort remain free of major functional disabilities (MFDs) at 24 months – – Expansion cohort enrolling additional patients to gain European manufacturing experience – CAMBRIDGE, Mass. --(BUSINESS WIRE)--Jun. 26, 2017-- bluebird bio, Inc.
06/23/17
Summary Togglebluebird bio Presents New Data from HGB-205 Study of LentiGlobinTM Drug Product in Patients with Transfusion-Dependent β-Thalassemia (TDT) and Severe Sickle Cell Disease (SCD) at European Hematology Association (EHA) Annual Meeting –Ongoing transfusion independence up to 3.5 years in patients with transfusion-dependent β-thalassemia (TDT); three patients have discontinued iron chelation – –First patient with severe sickle cell disease (SCD) treated with gene therapy continues to show clinically meaningful improvement in
06/23/17
Summary Togglebluebird bio Announces Early Data from Phase 3 Northstar-2 (HGB-207) Study of LentiGlobinTM Drug Product at European Hematology Association (EHA) Annual Meeting - Drug product vector copy number (DP VCN) and percentage of lentiviral vector positive cells (LVV+) for initial 7 drug product lots manufactured in Northstar -2 (HGB-207) are consistently higher than in Northstar (HGB-204) with median DP VCN of 3.0 – - Initial results show that the three patients
06/08/17
Summary Togglebluebird bio Appoints John O. Agwunobi, M.D. and Douglas A. Melton, Ph.D. to Board of Directors CAMBRIDGE, Mass. --(BUSINESS WIRE)--Jun. 8, 2017-- bluebird bio, Inc. ( Nasdaq: BLUE ), a clinical-stage company committed to developing potentially transformative gene therapies for severe genetic diseases and T cell-based immunotherapies for cancer, today announced that it has appointed John O.
06/05/17
Summary Togglebluebird bio and Celgene Corporation Announce Updated Clinical Results from Ongoing First-in-Human Multicenter Study of bb2121 Anti-BCMA CAR T Cell Therapy in Relapsed/Refractory Multiple Myeloma at ASCO Annual Meeting – 100% of the 15 evaluable patients in active dose cohorts (doses above 50 x 10 6 ) achieved an objective response; overall response rate (ORR) across all cohorts (n=18) is 89% – – 73% of evaluable patients in active dose cohorts achieved a very good partial response (VGPR) or better; 27% complete
06/01/17
Summary Togglebluebird bio to Present at Two Investor Conferences in June CAMBRIDGE, Mass. --(BUSINESS WIRE)--Jun. 1, 2017-- bluebird bio, Inc. ( Nasdaq: BLUE ), a clinical-stage company committed to developing potentially transformative gene therapies for severe genetic diseases and T cell-based immunotherapies for cancer, today announced that members of the management
05/23/17
Summary Togglebluebird bio Announces Collaboration with Duke University’s Robert J. Margolis, MD, Center for Health Policy on Value-Based Payment Framework for Gene Therapy – Collaboration includes industry leaders; aims to develop strategies for sustainable, value-based approach to access transformative gene therapy treatments – CAMBRIDGE, Mass. --(BUSINESS WIRE)--May 23, 2017-- bluebird bio, Inc. ( Nasdaq: BLUE ), a clinical-stage company committed to developing
05/18/17
Summary Togglebluebird bio to Present New Data from LentiGlobinTM Clinical Studies at European Hematology Association (EHA) Annual Meeting – Presentations include early data from Northstar -2 (HGB-207) study of LentiGlobin in patients with transfusion-dependent β-thalassemia (TDT) and non-β 0 /β 0 genotypes and updated data from HGB-205 study in TDT and severe sickle cell disease (SCD) – – Encore presentation of data from CRB-401
05/17/17
Summary Togglebluebird bio to Present Updated Clinical Results from Novel Anti-BCMA CAR T Cell Therapy bb2121 at American Society of Clinical Oncology (ASCO) Annual Meeting –Presentation will include safety and efficacy data from 18 patients with up to 12 months of follow-up– –Company to host event with live webcast, Monday, June 5 , 6:30 p.m. CT– CAMBRIDGE, Mass. --(BUSINESS WIRE)--May 17, 2017-- bluebird bio, Inc.
05/03/17
Summary Togglebluebird bio Reports First Quarter 2017 Financial Results and Recent Operational Progress – Case study on first patient with severe sickle cell disease (SCD) treated with gene therapy published in New England Journal of Medicine – – Appointed Derek Adams, Ph.D. Chief Technology and Manufacturing Officer and Joanne Smith-Farrell , Ph.D.
05/02/17
Summary Togglebluebird bio Enters Lentiviral Vector Patent License Agreement with GlaxoSmithKline for Commercialization of Gene Therapies CAMBRIDGE, Mass. --(BUSINESS WIRE)--May 2, 2017-- bluebird bio, Inc. (Nasdaq: BLUE) today announced that it has entered into a worldwide license agreement around its proprietary lentiviral vector platform with GlaxoSmithKline Intellectual Property Development Limited (GSK).
05/02/17
Summary Togglebluebird bio Licenses Lentiviral Vector Patent Rights for Development and Commercialization of Cell Therapies CAMBRIDGE, Mass. --(BUSINESS WIRE)--May 2, 2017-- bluebird bio, Inc. (Nasdaq: BLUE) today announced that it has entered into a worldwide license agreement around its proprietary lentiviral vector platform with Novartis Pharma AG . “bluebird bio is a pioneer in the field of lentiviral vector-based
04/26/17
Summary Togglebluebird bio to Present at Upcoming Investor Conferences CAMBRIDGE, Mass. --(BUSINESS WIRE)--Apr. 26, 2017-- bluebird bio, Inc. ( Nasdaq: BLUE ), a clinical-stage company committed to developing potentially transformative gene therapies for severe genetic diseases and T cell-based immunotherapies for cancer, today announced that members of the management
03/20/17
Summary Togglebluebird bio Appoints New Senior Manufacturing and Corporate Development Executives CAMBRIDGE, Mass. --(BUSINESS WIRE)--Mar. 20, 2017-- bluebird bio, Inc. ( Nasdaq: BLUE ), a clinical-stage company committed to developing potentially transformative gene therapies for severe genetic diseases and T cell-based immunotherapies for cancer, today announced that Derek Adams , Ph.D.
03/01/17
Summary Togglebluebird bio Announces Publication of Case Study on First Patient with Severe Sickle Cell Disease Treated with Gene Therapy in The New England Journal of Medicine – Patient treated with LentiGlobin TM drug product demonstrates high levels (~50% of total hemoglobin) of anti-sickling hemoglobin (HbA T87Q ) 15 months after treatment – CAMBRIDGE, Mass. --(BUSINESS WIRE)--Mar. 1, 2017-- bluebird bio, Inc. ( Nasdaq: BLUE ), a clinical-stage company committed to
02/28/17
Summary Togglebluebird bio to Present at Two Investor Conferences in March CAMBRIDGE, Mass. --(BUSINESS WIRE)--Feb. 28, 2017-- bluebird bio, Inc. ( Nasdaq: BLUE ), a clinical-stage company committed to developing potentially transformative gene therapies for severe genetic diseases and T cell-based immunotherapies for cancer, today announced that members of the management
02/22/17
Summary Togglebluebird bio Reports Fourth Quarter and Full Year 2016 Financial Results and Recent Operational Progress – Presented interim phase 1 dose escalation data for anti-BCMA CAR T product candidate in patients with relapsed/refractory multiple myeloma at EORTC-NCI-AACR Meeting – – Presented data from clinical studies of LentiGlobin TM drug product in patients with transfusion-dependent β-thalassemia (TDT)
02/03/17
Summary Togglebluebird bio Announces First Patient Treated with LentiGlobinTM Drug Product Under Amended Study Protocol in HGB-206 Phase 1 Study of Patients with Severe Sickle Cell Disease - LentiGlobin TM drug product had a vector copy number (DP VCN) of 3.3 copies/diploid genome, with 83% of cells lentiviral vector sequence positive (LVV+) – CAMBRIDGE, Mass. --(BUSINESS WIRE)--Feb. 3, 2017-- bluebird bio, Inc. ( Nasdaq: BLUE ), a clinical-stage company committed to developing
01/04/17
Summary Togglebluebird bio to Present at the 35th Annual J.P. Morgan Healthcare Conference CAMBRIDGE, Mass. --(BUSINESS WIRE)--Jan. 4, 2017-- bluebird bio, Inc. ( Nasdaq: BLUE ), a clinical-stage company committed to developing potentially transformative gene therapies for severe genetic diseases and T cell-based immunotherapies for cancer, announced today that Nick Leschly , chief

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(617) 245-2107

investor@bluebirdbio.com

 

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