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FDA Issues Emergency Use Authorization For Astrazeneca's Evusheld™ (Tixagevimab Co-packaged With Cilgavimab), The First Antibody Therapy Authorized In The U.S. For Pre-exposure Prophylaxis Of COVID-19

/PRNewswire/ Brand Institute is proud to announce its successful partnership with AstraZeneca in developing the brand name EVUSHELD™ and assisting with the.

MiamiFloridaUnited statesCanadaAmericanScott piergrossiJamesl dettoreDrug safety instituteBrand instituteWorld health organizationDrug administrationBrand institute incDrug safety institute teamAmerican medical associationAstrazenecaHealth canada

Brand Institute, Inc.: MHRA Approves XEVUDY (sotrovimab), GlaxoSmithKline and Vir Biotechnology's Monoclonal Antibody Treatment for Patients with COVID-19

The brand name XEVUDY was developed in partnership with Brand Institute, the global leader in pharmaceutical and healthcare-related name development MIAMI, Dec. 7, 2021 /PRNewswire/

MiamiFloridaUnited statesCanadaAmericanScott piergrossiJamesl dettoreDrug safety instituteGlaxosmithklineBrand instituteWorld health organizationRegulatory agencyDrug safety institute teamAmerican medical associationPrnewswire brand instituteHealth canada

MHRA Approves XEVUDY® (sotrovimab), GlaxoSmithKline and Vir Biotechnology's Monoclonal Antibody Treatment for Patients with COVID‑19

/PRNewswire/ Brand Institute is proud to announce its successful partnership with GlaxoSmithKline and Vir Biotechnology in developing the brand name.

MiamiFloridaUnited statesCanadaAmericanScott piergrossiJamesl dettoreDrug safety instituteGlaxosmithklineBrand instituteWorld health organizationRegulatory agencyBrand institute incDrug safety institute teamAmerican medical associationPrnewswire brand institute

FDA Approves Takeda's Livtencity™ (maribavir), First Treatment Approved for Post-Transplant Cytomegalovirus (CMV) Infection Resistant to Other Drugs

FDA Approves Takeda's Livtencity™ (maribavir), First Treatment Approved for Post-Transplant Cytomegalovirus (CMV) Infection Resistant to Other Drugs
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MiamiFloridaUnited statesCanadaAmericanScott piergrossipresidentJamesl dettoreDrug safety instituteBrand instituteWorld health organizationTakeda pharmaceuticals companyTakeda pharmaceuticalsBrand institute incDrug safety institute teamAmerican medical associationPrnewswire brand institute

FDA Approves Takeda's Livtencity™ (maribavir), First Treatment Approved for Post-Transplant Cytomegalovirus (CMV) Infection Resistant to Other Drugs

/PRNewswire/ Brand Institute is proud to announce its successful partnership with Takeda Pharmaceuticals Company Limited in naming the first treatment.

MiamiFloridaUnited statesCanadaAmericanScott piergrossiJamesl dettoreDrug safety instituteBrand instituteWorld health organizationTakeda pharmaceuticals companyTakeda pharmaceuticalsBrand institute incDrug safety institute teamAmerican medical associationPrnewswire brand institute