{"id":3531,"date":"2024-05-24T14:06:34","date_gmt":"2024-05-24T06:06:34","guid":{"rendered":"https:\/\/flcube.com\/?p=3531"},"modified":"2024-10-21T10:40:38","modified_gmt":"2024-10-21T02:40:38","slug":"sandoz-receives-european-commission-approval-for-biosimilars-wyost-and-jubbonti","status":"publish","type":"post","link":"https:\/\/flcube.com\/?p=3531","title":{"rendered":"Sandoz Receives European Commission Approval for Biosimilars Wyost and Jubbonti"},"content":{"rendered":"\n<p>The European Commission (EC) has granted registration approval to Sandoz, a Switzerland-headquartered pharmaceutical company (<a href=\"https:\/\/www.google.com\/finance\/quote\/SDZ:SWX\">SWX: SDZ<\/a>), for its biosimilars Wyost and Jubbonti. These products are reference treatments for Amgen\u2019s (<a href=\"https:\/\/www.google.com\/finance\/quote\/AMGN:NASDAQ\">NASDAQ: AMGN<\/a>) bone treatments Xgeva (denosumab) and Prolia (denosumab), respectively. Sandoz anticipates launching the biosimilars in November 2025.<\/p>\n\n\n\n<p>Wyost is indicated for the treatment of unresectable giant cell tumor of bone and for the prevention of skeletal-related events in patients with advanced malignancies involving bone. Jubbonti is approved for treating osteoporosis in postmenopausal women and in men who are at an increased risk of fractures or bone loss.<\/p>\n\n\n\n<p>According to the public data, Wyost and Jubbonti received approval in the U.S. market earlier this year.- <a href=\"https:\/\/flcube.com\">Flcube.com<\/a><\/p>\n\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>The European Commission (EC) has granted registration approval to Sandoz, a Switzerland-headquartered pharmaceutical company (SWX:&#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":[330,43,16,912,15,747,886],"class_list":["post-3531","post","type-post","status-publish","format-standard","hentry","category-company","category-drug","tag-amgen","tag-biosimilars","tag-cancer","tag-nasdaq-amgn","tag-product-approvals","tag-sandoz","tag-swx-sdz"],"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 European Commission Approval for Biosimilars Wyost and Jubbonti - Insight, China&#039;s Pharmaceutical Industry<\/title>\n<meta name=\"description\" content=\"The European Commission (EC) has granted registration approval to Sandoz, a Switzerland-headquartered pharmaceutical company (SWX: SDZ), for its biosimilars Wyost and Jubbonti. These products are reference treatments for Amgen\u2019s (NASDAQ: AMGN) bone treatments Xgeva (denosumab) and Prolia (denosumab), respectively. Sandoz anticipates launching the biosimilars in November 2025.\" \/>\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=3531\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Sandoz Receives European Commission Approval for Biosimilars Wyost and Jubbonti\" \/>\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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