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Regeneron (REGN) and Sanofi (SNY) Report Dupixent Shows Significant Improvements in Signs and Symptoms of Moderate-to-severe Atopic Hand and Foot Dermatitis

Regeneron (REGN) and Sanofi (SNY) Report Dupixent Shows Significant Improvements in Signs and Symptoms of Moderate-to-severe Atopic Hand and Foot Dermatitis
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United statesRegeneron velocimmune technologyregeneronEricl simpsonGeorged yancopoulosFrancesj storrsScience universityRegeneron pharmaceuticals incRegeneron genetics centerOregon healthExchange commissionAmerican academy of dermatologyEuropean unionDupilumab development programdupilumabWall streetAmerican academyMedical dermatology

Dupixent® (dupilumab) Late-Breaking Data at AAD Show Significant Improvements in Signs and Symptoms of Moderate-to-severe Atopic Hand and Foot Dermatitis

Dupixent® (dupilumab) Late-Breaking Data at AAD Show Significant Improvements in Signs and Symptoms of Moderate-to-severe Atopic Hand and Foot Dermatitis
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United statesFrance generalRegeneron velocimmune technologyregeneronEricl simpsonGeorged yancopoulosFrancesj storrsScience universityRegeneron pharmaceuticals incRegeneron genetics centerOregon healthExchange commissionAmerican academy of dermatologyEuropean unionDupilumab development programdupilumabAmerican academyMedical dermatology

Gritstone bio Announces Presentations on Neoantigen Prediction Capabilities and Cancer Vaccine Programs at the 2023 AACR Annual Meeting

Gritstone bio Announces Presentations on Neoantigen Prediction Capabilities and Cancer Vaccine Programs at the 2023 AACR Annual Meeting
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United statesOrange county convention centerDan budwickMatthew davisAnkur dhanikChristine palmerGeorgee macdougalldirectorExchange commissionAmerican association for cancer researchCancer researchAnnual meetingPoster presentationTuesday aprArtificial intelligenceDeep learningPoster section

Vir Biotechnology (VIR) Reports Positive Final Draft Guidance on Sotrovimab from the UK s National Institute for Health and Care Excellence

Vir Biotechnology (VIR) Reports Positive Final Draft Guidance on Sotrovimab from the UK s National Institute for Health and Care Excellence
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United kingdomCarly scadutoGeorge scangosExchange commissionUnited kingdom national health serviceVir biotechnology incUnited kingdom national institute for healthXencor incNational instituteCare excellenceChief executive officerNational health serviceVir biotechnologyvir biotechnologyForward looking statementsthisPrivate securities litigation reform actVir biotechnology

Takeda Presents Positive Results from Phase 3 Study of Vedolizumab for Prevention of Intestinal Acute Graft-Versus-Host Disease (aGvHD) in Patients Undergoing Allogeneic Hematopoietic Stem Cell Transplantation (allo-HSCT)

Takeda Presents Positive Results from Phase 3 Study of Vedolizumab for Prevention of Intestinal Acute Graft-Versus-Host Disease (aGvHD) in Patients Undergoing Allogeneic Hematopoietic Stem Cell Transplantation (allo-HSCT)
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United statesBin chenJohn cunninghamChinwe ukomaduCrohn diseasevedolizumabCancer centerInternational blood marrow transplant researchHematopoietic cell transplant therapy programExchange commissionEuropean unionEuropean medicines agencyTakeda pharmaceutical company limitedYi bin chenHematopoietic cell transplantCell therapy programMass general cancer