{"id":14664,"date":"2023-08-28T18:29:00","date_gmt":"2023-08-28T10:29:00","guid":{"rendered":"https:\/\/flcube.com\/?p=14664"},"modified":"2024-11-24T18:32:29","modified_gmt":"2024-11-24T10:32:29","slug":"sandoz-receives-fda-clearance-for-first-biosimilar-to-biogens-tysabri","status":"publish","type":"post","link":"https:\/\/flcube.com\/?p=14664","title":{"rendered":"Sandoz Receives FDA Clearance for First Biosimilar to Biogen&#8217;s Tysabri"},"content":{"rendered":"\n<p>The Sandoz unit of Switzerland-based Novartis (<a href=\"https:\/\/www.google.com\/finance\/quote\/NVS:NYSE\">NYSE: NVS<\/a>) has received regulatory clearance from the US Food and Drug Administration (FDA) for Tyruko (natalizumab), marking it as the first biosimilar version referencing Biogen&#8217;s (<a href=\"https:\/\/www.google.com\/finance\/quote\/BIIB:NASDAQ\">NASDAQ: BIIB<\/a>) blockbuster biologic Tysabri. Both monoclonal antibodies (mAbs) are indicated for treating Crohn\u2019s disease and relapsing forms of multiple sclerosis (MS), including clinically isolated syndrome (CIS), relapsing-remitting MS (RRMS), and active secondary progressive disease.<\/p>\n\n\n\n<p><strong>Equivalence in Efficacy, Safety, and Immunogenicity<\/strong><br>The approval was supported by results from Phase I and Phase III studies, which demonstrated that Sandoz\u2019s biosimilar is equivalent to Biogen\u2019s originator in terms of efficacy, safety, and immunogenicity. This equivalence is crucial for patients and healthcare providers, ensuring that they have access to a cost-effective alternative without compromising on the quality and effectiveness of treatment.<\/p>\n\n\n\n<p><strong>Sandoz&#8217;s Global Commercialization Rights and Impact on Tysabri Sales<\/strong><br>Sandoz in-licensed Tyruko from Polpharma Biologics in 2019 and currently holds global commercialization and distribution rights for the biosimilar. The introduction of Tyruko is expected to erode Tysabri\u2019s sales, which reached USD 2.0 billion in 2022, making it Biogen\u2019s top-selling drug. The entry of a biosimilar provides a significant opportunity to increase patient access to this critical therapy while potentially reducing healthcare costs.<a href=\"https:\/\/flcube.com\/\">-Fineline Info &amp; Tech<\/a><\/p>\n\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>The Sandoz unit of Switzerland-based Novartis (NYSE: NVS) has received regulatory clearance from the US&#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":[65,351,43,622,993,140,865,15],"class_list":["post-14664","post","type-post","status-publish","format-standard","hentry","category-company","category-drug","tag-auto-immune","tag-biogen","tag-biosimilars","tag-gastroenterology","tag-nasdaq-biib","tag-novartis","tag-nyse-nvs","tag-product-approvals"],"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>Sandoz Receives FDA Clearance for First Biosimilar to Biogen&#039;s Tysabri - Insight, China&#039;s Pharmaceutical Industry<\/title>\n<meta name=\"description\" content=\"The Sandoz unit of Switzerland-based Novartis (NYSE: NVS) has received regulatory clearance from the US Food and Drug Administration (FDA) for Tyruko (natalizumab), marking it as the first biosimilar version referencing Biogen&#039;s (NASDAQ: BIIB) blockbuster biologic Tysabri. Both monoclonal antibodies (mAbs) are indicated for treating Crohn\u2019s disease and relapsing forms of multiple sclerosis (MS), including clinically isolated syndrome (CIS), relapsing-remitting MS (RRMS), and active secondary progressive disease.\" \/>\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=14664\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Sandoz Receives FDA Clearance for First Biosimilar to Biogen&#039;s Tysabri\" \/>\n<meta property=\"og:description\" content=\"Navigate the complexities of China\u2019s pharmaceutical industry with precision and clarity. FLCUBE delivers reliable data, news, and intelligence to broaden your horizons and sharpen your decision-making. 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