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Prime Therapeutics and Takeda agree to outcomes-based arrangement for Hemophilia A treatment ADVATE® [Antihemophilic Factor (Recombinant)]

Share: EAGAN, Minn., Dec. 16, 2020 /PRNewswire/  In an effort to help assess the value of hemophilia A treatments relative to total health care costs and emergency department visits, Prime Therapeutics LLC (Prime) has finalized an arrangement with Takeda Pharmaceuticals America, Inc., a wholly-owned subsidiary of Takeda Pharmaceutical Company Limited (NYSE:TAK) ( Takeda ) for the factor replacement product ADVATE ® [Antihemophilic Factor (Recombinant)], which is used in the treatment and prevention of bleeding episodes in patients with hemophilia A (congenital factor VIII deficiency). Hemophilia treatment options have increased in recent years, including innovative therapies. However, these innovations come at a high price. Therefore, it is important to establish integrated medical and pharmacy benefit contracts between payers and product manufacturers on existing treatments. The arrangement between Prime and Takeda provides:

U S Food and Drug Administration Accepts New Drug Application for Review, Grants Priority Review for Takeda s TAK-721 (budesonide oral suspension) for the Treatment of Eosinophilic Esophagitis

U S Food and Drug Administration Accepts New Drug Application for Review, Grants Priority Review for Takeda s TAK-721 (budesonide oral suspension) for the Treatment of Eosinophilic Esophagitis
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U S Food and Drug Administration Accepts New Drug Application for Review, Grants Priority Review for Takeda s TAK-721 (budesonide oral suspension) for the Treatment of Eosinophilic Esophagitis | Business

U S Food and Drug Administration Accepts New Drug Application for Review, Grants Priority Review for Takeda s TAK-721 (budesonide oral suspension) for the Treatment of Eosinophilic Esophagitis | Business
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