{"id":8482,"date":"2024-02-26T23:07:28","date_gmt":"2024-02-26T15:07:28","guid":{"rendered":"https:\/\/flcube.com\/?p=8482"},"modified":"2024-10-21T23:09:45","modified_gmt":"2024-10-21T15:09:45","slug":"takedas-recombinant-pig-fviii-drug-for-acquired-hemophilia-a-approved-in-china","status":"publish","type":"post","link":"https:\/\/flcube.com\/?p=8482","title":{"rendered":"Takeda&#8217;s Recombinant Pig FVIII Drug for Acquired Hemophilia A Approved in China"},"content":{"rendered":"\n<p>The National Medical Products Administration (NMPA) website has indicated that Takeda (<a href=\"https:\/\/www.google.com\/finance\/quote\/4502:TYO\">TYO: 4502<\/a>)&#8217;s Obizur (susoctocog alfa), intended for on-demand treatment and control of bleeding events in adult patients with acquired hemophilia A, has received approval in China. This drug marks the first recombinant pig FVIII (rpFVIII) to be approved by both the FDA and EMA for acquired hemophilia A treatment. Susoctocog alfa boasts a structure and sequence homologous to human factor VIII (FVIII), and its resistance to inactivation by anti-human FVIII autoantibodies allows it to effectively replace human FVIII in hemostasis.<\/p>\n\n\n\n<p>Takeda acquired susoctocog alfa through its $62 billion purchase of Shire in 2018, which had previously acquired the originator company Baxalta for $32 billion in 2016.- <a href=\"https:\/\/flcube.com\">Flcube.com<\/a><\/p>\n\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>The National Medical Products Administration (NMPA) website has indicated that Takeda (TYO: 4502)&#8217;s Obizur (susoctocog&#8230;<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"googlesitekit_rrm_CAownpewDA:productID":"","_jetpack_memberships_contains_paid_content":false,"footnotes":"","jetpack_publicize_message":"","jetpack_publicize_feature_enabled":true,"jetpack_social_post_already_shared":false,"jetpack_social_options":{"image_generator_settings":{"template":"highway","default_image_id":0,"font":"","enabled":false},"version":2}},"categories":[7,11],"tags":[15,345,1141],"class_list":["post-8482","post","type-post","status-publish","format-standard","hentry","category-company","category-drug","tag-product-approvals","tag-takeda","tag-tyo-4502"],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v23.6 (Yoast SEO v27.5) - https:\/\/yoast.com\/product\/yoast-seo-premium-wordpress\/ -->\n<title>Takeda&#039;s Recombinant Pig FVIII Drug for Acquired Hemophilia A Approved in China - Insight, China&#039;s Pharmaceutical Industry<\/title>\n<meta name=\"description\" content=\"The National Medical Products Administration (NMPA) website has indicated that Takeda (TYO: 4502)&#039;s Obizur (susoctocog alfa), intended for on-demand treatment and control of bleeding events in adult patients with acquired hemophilia A, has received approval in China. This drug marks the first recombinant pig FVIII (rpFVIII) to be approved by both the FDA and EMA for acquired hemophilia A treatment. Susoctocog alfa boasts a structure and sequence homologous to human factor VIII (FVIII), and its resistance to inactivation by anti-human FVIII autoantibodies allows it to effectively replace human FVIII in hemostasis.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/flcube.com\/?p=8482\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Takeda&#039;s Recombinant Pig FVIII Drug for Acquired Hemophilia A Approved in China\" \/>\n<meta property=\"og:description\" content=\"Navigate the complexities of China\u2019s pharmaceutical industry with precision and clarity. 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