{"id":3355,"date":"2024-05-30T12:12:38","date_gmt":"2024-05-30T04:12:38","guid":{"rendered":"https:\/\/flcube.com\/?p=3355"},"modified":"2024-10-20T15:09:07","modified_gmt":"2024-10-20T07:09:07","slug":"amgens-bkemv-becomes-first-biosimilar-to-challenge-astrazenecas-soliris-with-fda-approval","status":"publish","type":"post","link":"https:\/\/flcube.com\/?p=3355","title":{"rendered":"Amgen&#8217;s Bkemv Becomes First Biosimilar to Challenge AstraZeneca&#8217;s Soliris with FDA Approval"},"content":{"rendered":"\n<p>Amgen Inc. (<a href=\"https:\/\/www.google.com\/finance\/quote\/AMGN:NASDAQ\">NASDAQ: AMGN<\/a>), a leading biopharmaceutical company, has been granted regulatory approval by the US Food and Drug Administration (FDA) for Bkemv, marking a significant milestone as the first biosimilar in the US to compete with AstraZeneca\u2019s (AZ; <a href=\"https:\/\/www.google.com\/finance\/quote\/AZN:NASDAQ\">NASDAQ: AZN<\/a>) Soliris (eculizumab). Both the originator drug from AstraZeneca and Amgen\u2019s biosimilar are indicated for the treatment of paroxysmal nocturnal hemoglobinuria (PNH) and atypical hemolytic uremic syndrome (aHUS).<\/p>\n\n\n\n<p>Bkemv has been awarded interchangeable biosimilar status, signifying that it can be substituted for the reference product in certain cases. However, due to the serious safety concerns associated with the biologic, Bkemv will only be made available to patients who have completed a risk evaluation and mitigation strategy (REMS) program.- <a href=\"https:\/\/flcube.com\">Flcube.com<\/a><\/p>\n\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Amgen Inc. (NASDAQ: AMGN), a leading biopharmaceutical company, has been granted regulatory approval by the&#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":[330,130,770,43,912,871,15,24],"class_list":["post-3355","post","type-post","status-publish","format-standard","hentry","category-company","category-drug","tag-amgen","tag-astrazeneca","tag-az","tag-biosimilars","tag-nasdaq-amgn","tag-nasdaq-azn","tag-product-approvals","tag-rare-orphan-disease-drugs"],"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>Amgen&#039;s Bkemv Becomes First Biosimilar to Challenge AstraZeneca&#039;s Soliris with FDA Approval - Insight, China&#039;s Pharmaceutical Industry<\/title>\n<meta name=\"description\" content=\"Amgen Inc. (NASDAQ: AMGN), a leading biopharmaceutical company, has been granted regulatory approval by the US Food and Drug Administration (FDA) for Bkemv, marking a significant milestone as the first biosimilar in the US to compete with AstraZeneca\u2019s (AZ; NASDAQ: AZN) Soliris (eculizumab). 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