{"id":10592,"date":"2024-10-31T14:13:33","date_gmt":"2024-10-31T06:13:33","guid":{"rendered":"https:\/\/flcube.com\/?p=10592"},"modified":"2024-10-31T14:13:38","modified_gmt":"2024-10-31T06:13:38","slug":"shanghai-henlius-and-organon-submit-biosimilar-application-for-denosumab-to-fda","status":"publish","type":"post","link":"https:\/\/flcube.com\/?p=10592","title":{"rendered":"Shanghai Henlius and Organon Submit Biosimilar Application for Denosumab to FDA"},"content":{"rendered":"\n<p>Shanghai Henlius Biotech Inc. (<a href=\"https:\/\/www.google.com\/finance\/quote\/2696:HKG\">HKG: 2696<\/a>) and its US partner Organon (<a href=\"https:\/\/www.google.com\/finance\/quote\/OGN:NYSE\">NYSE: OGN<\/a>) have jointly announced that the Biologic License Application (BLA) for HLX14, an investigational biosimilar of Amgen\u2019s (<a href=\"https:\/\/www.google.com\/finance\/quote\/AMGN:NASDAQ\">NASDAQ: AMGN<\/a>) Prolia\/Xgeva (denosumab), has been accepted for review by the US Food and Drug Administration (FDA).<\/p>\n\n\n\n<p>Denosumab, a recombinant anti-RANKL human monoclonal antibody injection, is indicated for various conditions, including the treatment of postmenopausal women with osteoporosis at high risk of fracture, certain patients with giant cell tumor of bone, skeletal-related events in patients with multiple myeloma, and patients with bone metastases from solid tumors. In June 2022, Henlius entered into a licensing agreement with Organon, granting the company exclusive commercialization rights to Henlius&#8217;s biosimilars of Perjeta (pertuzumab, HLX11) and Prolia\/Xgeva (denosumab, HLX14) in global territories outside Greater China.- <a href=\"https:\/\/flcube.com\">Flcube.com<\/a><\/p>\n\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Shanghai Henlius Biotech Inc. (HKG: 2696) and its US partner Organon (NYSE: OGN) have jointly&#8230;<\/p>\n","protected":false},"author":1,"featured_media":10593,"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":[330,270,38,912,972,174],"class_list":["post-10592","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-company","category-drug","tag-amgen","tag-henlius-biotech","tag-market-approval-filings","tag-nasdaq-amgn","tag-nyse-ogn","tag-organon"],"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>Shanghai Henlius and Organon Submit Biosimilar Application for Denosumab to FDA - Insight, China&#039;s Pharmaceutical Industry<\/title>\n<meta name=\"description\" content=\"Shanghai Henlius Biotech Inc. (HKG: 2696) and its US partner Organon (NYSE: OGN) have jointly announced that the Biologic License Application (BLA) for HLX14, an investigational biosimilar of Amgen\u2019s (NASDAQ: AMGN) Prolia\/Xgeva (denosumab), has been accepted for review by the US Food and Drug Administration (FDA).\" \/>\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=10592\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Shanghai Henlius and Organon Submit Biosimilar Application for Denosumab to FDA\" \/>\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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