Media Room Menu
Month Year
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Month Year
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Feb 6, 2020JDRF T1D Fund Study Estimates 2.3 Million People at Risk Globally to Develop Stage 3 T1D, Which Already Affects 18 Million People Globally
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Jan 30, 2020- Acid sphingomyelinase deficiency (ASMD) is a rare, progressive and potentially life-threatening disease for which no treatments are approved
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Jan 28, 2020If approved, Dupixent would be the first biologic medicine available in the U.S. for these children
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Jan 23, 2020* Synthorx, Inc. is now a fully owned subsidiary of Sanofi
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Dec 12, 2019Expects to Complete Submission of a BLA for PRV-031 (Teplizumab) in Q4 2020
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Dec 9, 2019- U.S.-based, state of the art facilities to be established for sustainable production of adjuvanted recombinant vaccine for use in the event of a pandemic
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Nov 21, 2019- Sutimlimab, an investigational targeted C1s inhibitor, met its primary efficacy endpoint in Phase 3 trial for patients with cold agglutinin disease (CAD)
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Nov 6, 2019*Oncology: New data from investigational isatuximab pivotal study for the treatment of relapsed/refractory multiple myeloma
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Nov 5, 2019- PRV-031 (teplizumab) Granted Breakthrough Therapy and PRIME Designations -
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Nov 4, 2019* Will be available in fall 2020, in time for the 2020-2021 flu season
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Oct 22, 2019-Study Did Not Achieve Primary Endpoint Due to High Placebo Effect-
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Oct 15, 2019- One of the first digital manufacturing facilities in the world to use continuous, intensified biologics production technology
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Oct 9, 2019Add-on payment to provide additional Medicare reimbursement for Medicare patients prescribed Cablivi in eligible hospital inpatient settings
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Sep 30, 2019- CARD is a treatment sequencing trial investigating the efficacy and safety of Jevtana versus abiraterone or enzalutamide after disease progression following initial androgen receptor-targeted agent therapy and docetaxel
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Sep 26, 2019- T1D Fund Executive Chairman and Former Bain Capital Managing Director Brings Extensive Financial Expertise and Deep Knowledge of Therapeutics Landscape -
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Sep 24, 2019- FDA Meeting Expected in Q4 2019 and BLA Submission for PRV-031 (teplizumab) Targeted for Q4 2020 -