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U S FDA Extends Review of Biologics License Application for REGEN-COV® (casirivimab and imdevimab) for Treatment and Prophylaxis of COVID-19

/PRNewswire/ Regeneron Pharmaceuticals, Inc. (NASDAQ: REGN) today announced that the U.S. Food and Drug Administration (FDA) has extended by three months.

United statesGeorged yancopoulosTammy allenRegeneron velocimmuneVesna tosicCenters for diseasePrnewswire regeneron pharmaceuticals incRegeneron pharmaceuticals incUs department of healthRegeneron genetics centerHuman service office of theBiomedical advanced researchDrug administrationDevelopment authorityRegeneron velocimmune technologyTeva pharmaceutical industries ltd

FDA Accepts REGEN-COV® (casirivimab and imdevimab) for Priority Review for Treatment and Prophylaxis of COVID-19

/PRNewswire/ Regeneron Pharmaceuticals, Inc. (NASDAQ: REGN) today announced that the U.S. Food and Drug Administration (FDA) has accepted for priority.

United statesUnited kingdomSouth africaSeptember regeneronGeorged yancopoulosTammy allenRegeneron velocimmuneVesna tosicHuman service office of theRegeneron velocimmune technologyTeva pharmaceutical industries ltdDepartment of healthEuropean unionPharmaceuticals incCenters for diseaseRegeneron pharmaceuticals inc

New REGEN-COV™ (casirivimab and imdevimab) Data Show Supportive Results in Patients Hospitalized with COVID-19

Press release content from PR Newswire. The AP news staff was not involved in its creation.

United statesUnited kingdomSouth africaEleftherios mylonakisGeorged yancopoulosTammy allenRegeneron velocimmuneVesna tosicHuman service office of theRegeneron velocimmune technologyTeva pharmaceutical industries ltdDepartment of healthEuropean unionCenters for diseaseRegeneron pharmaceuticals incBiomedical advanced research

New England Journal of Medicine Publishes Positive Phase 3 Trial Results for REGEN-COV™ (casirivimab and imdevimab) to Treat COVID-19

New England Journal of Medicine Publishes Positive Phase 3 Trial Results for REGEN-COV™ (casirivimab and imdevimab) to Treat COVID-19
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United statesUnited kingdomSouth africaGeorged yancopoulosTammy allenRegeneron velocimmuneVesna tosicHuman service office of theRegeneron velocimmune technologyAmerican thoracic society international conferenceTeva pharmaceutical industries ltdDepartment of healthEuropean unionPharmaceuticals incCenters for diseaseRegeneron pharmaceuticals inc