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FDA approves Dupixent® (dupilumab) for moderate-to-severe atopic dermatitis in adolescents - March 11, 2019
3/11/2019
In a Phase 3 trial, Dupixent significantly reduced the extent and severity of disease and itching, and helped adolescents achieve clearer skin
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New Genetic Data from Regeneron and GSK on 50,000 UK Biobank Participants Made Available to Global Health Research Community
3/11/2019
Represents first tranche to be released; data from all 500,000 UK Biobank participants will ultimately be made available via larger biopharma consortium effort
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CHMP Recommends Approval of Dupixent® (dupilumab) for Asthma Indication
3/1/2019
Regeneron Pharmaceuticals, Inc. and Sanofi announced that the European Medicines Agency's Committee for Medicinal Products for Human Use has adopted a positive opinion for Dupixent® in asthma.
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New Analyses to Be Presented at AAD for Dupixent® (dupilumab) and the Burden of Atopic Dermatitis
3/1/2019
Regeneron Pharmaceuticals, Inc. and Sanofi announced that the companies will present a diverse set of clinical and real-world data at the 2019 American Academy of Dermatology Annual Meeting from March 1 to 5 in Washington, D.C.
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Positive Results Presented from Two Phase 3 Trials of Dupixent® (dupilumab) in Severe Chronic Rhinosinusitis with Nasal Polyps (CRSwNP)
2/25/2019
Dupixent showed significant improvement on every primary and secondary endpoint in patients with severe CRSwNP who had failed previous treatment with surgery and/or systemic corticosteroids
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U.S. and EU Patent Office Decisions Invalidate Amgen Subsidiary Immunex's Patents Claiming Antibodies to the IL-4 Receptor
2/15/2019
Today the European Patent Office invalidated Immunex's European patent claiming antibodies that target human IL-4 receptors (IL-4R)
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Sanofi and Regeneron offer Praluent® (alirocumab) at a new reduced U.S. list price
2/11/2019
This is the latest step by the companies to help make Praluent more accessible and affordable for appropriate patients
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Regeneron and Sanofi Offer Praluent® (alirocumab) at a New Reduced U.S. List Price
2/11/2019
This is the latest step by the companies to help make Praluent more accessible and affordable for appropriate patients
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One-Year Results from Positive Phase 3 EYLEA Trial in Diabetic Retinopathy Presented at Angiogenesis Symposium
2/9/2019
Trial showed that early intervention with EYLEA improved diabetic retinopathy severity and prevented serious vision-threatening complications
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Thirteen of those were development programs, the remaining 25 research-stage. In September, the company indicated it was on a cost-cutting program, planning to save 1.5 billion euros this year. Of the programs it is dumping, the most prominent is a mid-phase drug for respiratory syncytial virus (...
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Sanofi delivers 2018 business EPS growth of 5.1% at CER
2/7/2019
Net sales were €8,997 million, an increase of 3.5% on a reported basis, 3.9%(3) at CER and 2.6% at CER/CS (4).
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Regeneron Reports Fourth Quarter and Full Year 2018 Financial and Operating Results
2/6/2019
Regeneron Pharmaceuticals, Inc. announced financial results for the fourth quarter and full year 2018 and provided a business update.
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Regeneron and Sanofi Restructure Immuno-Oncology Collaboration for Discovery and Development Programs
1/7/2019
Companies select two clinical-stage bispecific antibodies for ongoing collaboration
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Regeneron Provides Update on Commercial and Pipeline Progress at J.P. Morgan Healthcare Conference
1/7/2019
Regeneron Pharmaceuticals, Inc. will provide a strategic business update to the investor community at the 37th Annual J.P. Morgan Healthcare Conference
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Harbour BioMed Appoints Atul Deshpande, Ph.D. MBA, Chief Strategy Officer and Head of U.S. Operations
1/4/2019
Company also promotes Xiaoxiang Chen, MD, to Chief Development Officer, and Mai-Jing Liao, Ph.D., MBA to Chief Business Officer
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United Neuroscience Names Peter Powchik, M.D, Executive Vice President of Research & Development
12/21/2018
United Neuroscience (UNS), a clinical-stage biotech company pioneering a new class of medicine to treat and prevent brain disorders, today announced the appointment of Peter Powchik, M.D., to the newly created position of Executive Vice President of Research & Development effective Jan. 1, 2019.
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Regeneron Presents Positive Data at ASH for REGN1979 CD20xCD3 Bispecific Antibody in Relapsed or Refractory B-Cell Non-Hodgkin Lymphoma
12/1/2018
100% overall and 80% complete response rate in 10 patients with relapsed or refractory follicular lymphoma treated with 5 mg or more of REGN1979
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ODYSSEY OUTCOMES Investigators Highlight at AHA that Praluent® (alirocumab) Injection Was Associated with Fewer Deaths from Any Cause
11/11/2018
Mortality risk reduction greater in patients treated for at least 3 years or those with baseline LDL-C levels of at least 100 mg/dL
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New England Journal of Medicine publishes positive detailed results from Praluent® (alirocumab) Injection cardiovascular outcomes trial
11/7/2018
Praluent significantly reduced major adverse cardiovascular events by 15% (p<0.001)
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FDA Grants Priority Review for Dupixent® (dupilumab) as Potential Treatment for Adolescents with Uncontrolled Moderate-to-Severe Atopic Dermatitis
11/6/2018
Regeneron Pharmaceuticals, Inc. and Sanofi today announced that the U.S. Food and Drug Administration (FDA) has accepted for Priority Review the supplemental Biologics License Application (sBLA) for Dupixent® (dupilumab) in adolescent patients 12 to 17 years of age with moderate-to-severe atopic dermatitis, whose disease was inadequately controlled with topical therapies or for whom topical treatment was medically inadvisable.