{"id":9295,"date":"2024-01-30T20:13:00","date_gmt":"2024-01-30T12:13:00","guid":{"rendered":"https:\/\/flcube.com\/?p=9295"},"modified":"2024-10-24T20:15:33","modified_gmt":"2024-10-24T12:15:33","slug":"takedas-gammagard-liquid-approved-by-fda-for-chronic-inflammatory-demyelinating-polyneuropathy","status":"publish","type":"post","link":"https:\/\/flcube.com\/?p=9295","title":{"rendered":"Takeda\u2019s Gammagard Liquid Approved by FDA for Chronic Inflammatory Demyelinating Polyneuropathy"},"content":{"rendered":"\n<p>The US Food and Drug Administration (FDA) has granted regulatory approval for Takeda\u2019s (<a href=\"https:\/\/www.google.com\/finance\/quote\/4502:TYO\">TYO: 4502<\/a>) plasma-derived therapy Gammagard Liquid, a human immune globulin, for use as induction therapy and treatment for chronic inflammatory demyelinating polyneuropathy (CIDP) in adults. This decision is supported by clinical data demonstrating that the intravenous immunoglobulin (IVIG) improved functional disability in 94.4% of study participants.<\/p>\n\n\n\n<p>As stated in the press release, Gammagard Liquid is also approved in the US for the treatment of primary immunodeficiency and the neuromuscular disorder known as multifocal motor neuropathy.- <a href=\"https:\/\/flcube.com\">Flcube.com<\/a><\/p>\n\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>The US Food and Drug Administration (FDA) has granted regulatory approval for Takeda\u2019s (TYO: 4502)&#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":[15,24,345,1141],"class_list":["post-9295","post","type-post","status-publish","format-standard","hentry","category-company","category-drug","tag-product-approvals","tag-rare-orphan-disease-drugs","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\u2019s Gammagard Liquid Approved by FDA for Chronic Inflammatory Demyelinating Polyneuropathy - Insight, China&#039;s Pharmaceutical Industry<\/title>\n<meta name=\"description\" content=\"The US Food and Drug Administration (FDA) has granted regulatory approval for Takeda\u2019s (TYO: 4502) plasma-derived therapy Gammagard Liquid, a human immune globulin, for use as induction therapy and treatment for chronic inflammatory demyelinating polyneuropathy (CIDP) in adults. 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