{"id":23031,"date":"2023-01-09T23:35:00","date_gmt":"2023-01-09T15:35:00","guid":{"rendered":"https:\/\/flcube.com\/?p=23031"},"modified":"2025-01-28T02:07:47","modified_gmt":"2025-01-27T18:07:47","slug":"suzhou-therys-generic-nilotinib-approved-by-chinas-nmpa","status":"publish","type":"post","link":"https:\/\/flcube.com\/?p=23031","title":{"rendered":"Suzhou Thery&#8217;s Generic Nilotinib Approved by China&#8217;s NMPA"},"content":{"rendered":"\n<p>China-based Suzhou Thery Pharmaceutical Inc. has announced that the National Medical Products Administration (NMPA) has approved its generic version of Novartis&#8217;s (<a href=\"https:\/\/www.google.com\/finance\/quote\/NVS:NYSE\">NYSE: NVS<\/a>) cancer therapy Tasigna (nilotinib). Thery filed a \u201c4.1 certification\u201d under China\u2019s patent linkage system, directly challenging the validity of Tasigna\u2019s patent. Thery is the first company to successfully do so since the linkage system was established in July 2021.<\/p>\n\n\n\n<p><strong>Patent Linkage System and Market Exclusivity<\/strong><br>Under China\u2019s patent linkage system rules, the first generic company to file a 4.1 certification against an originator drug and successfully win both the patent challenge case and approval is awarded 12 months\u2019 market exclusivity alongside the originator. This means that no further generic will be approved for one year. <a href=\"https:\/\/flcube.com\/\">Fineline Info &amp; Tech<\/a>\u2019s IP Radar system shows that Suzhou Thery\u2019s 4.1 filing was first publicized by the Center for Drug Evaluation (CDE) in November 2021, while Qilu Pharmaceutical made a 4.2 category filing (indicating that it viewed its generic as non-infringing) two months later.<\/p>\n\n\n\n<p><strong>Therapeutic Profile and Market Impact<\/strong><br>Nilotinib is a tyrosine kinase inhibitor (TKI) used to treat chronic myeloid leukemia (CML), particularly in patients resistant or intolerant to first-generation TKI imatinib. <a href=\"https:\/\/flcube.com\/\">Fineline Info &amp; Tech<\/a> data show that Novartis\u2019s compound patent for nilotinib was not expected to expire until 2026, and it also had an indication patent running until 2030. Thery Pharma boasts 14 products with generic quality consistency evaluation (GQCE) qualification, alongside 29 active pharmaceutical ingredients (APIs) with registration numbers in China.<\/p>\n\n\n\n<p><strong>Future Outlook<\/strong><br>The approval of Thery\u2019s generic version of nilotinib highlights the company\u2019s strategic approach to challenging patents and expanding its market presence. With 12 months of market exclusivity, Thery is well-positioned to capture a significant share of the market for this essential cancer therapy. The company\u2019s ongoing efforts in generic drug development underscore its commitment to providing affordable and high-quality medications to patients.<a href=\"https:\/\/flcube.com\/\">-Fineline Info &amp; Tech<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>China-based Suzhou Thery Pharmaceutical Inc. has announced that the National Medical Products Administration (NMPA) has&#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":[16,42,140,865,73,15,3300],"class_list":["post-23031","post","type-post","status-publish","format-standard","hentry","category-company","category-drug","tag-cancer","tag-first-mover-generic","tag-novartis","tag-nyse-nvs","tag-patents","tag-product-approvals","tag-thery-pharmaceutical"],"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>Suzhou Thery&#039;s Generic Nilotinib Approved by China&#039;s NMPA - Insight, China&#039;s Pharmaceutical Industry<\/title>\n<meta name=\"description\" content=\"China-based Suzhou Thery Pharmaceutical Inc. has announced that the National Medical Products Administration (NMPA) has approved its generic version of Novartis&#039;s (NYSE: NVS) cancer therapy Tasigna (nilotinib). Thery filed a \u201c4.1 certification\u201d under China\u2019s patent linkage system, directly challenging the validity of Tasigna\u2019s patent. Thery is the first company to successfully do so since the linkage system was established in July 2021.\" \/>\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=23031\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Suzhou Thery&#039;s Generic Nilotinib Approved by China&#039;s NMPA\" \/>\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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