{"id":3870,"date":"2026-06-07T06:35:40","date_gmt":"2026-06-07T13:35:40","guid":{"rendered":"https:\/\/xpharma.com.cn\/?p=3870"},"modified":"2026-06-07T06:35:41","modified_gmt":"2026-06-07T13:35:41","slug":"bristol-myers-squibb-camzyos-mavacamten-supplemental-new-drug-application-snda-accepted-by-the-u-s-fda","status":"publish","type":"post","link":"https:\/\/xpharma.com.cn\/index.php\/news\/bristol-myers-squibb-camzyos-mavacamten-supplemental-new-drug-application-snda-accepted-by-the-u-s-fda\/","title":{"rendered":"Bristol Myers Squibb: Camzyos mavacamten supplemental New Drug Application (sNDA) accepted by the U.S. FDA."},"content":{"rendered":"\n<p class=\"wp-block-paragraph\">On June 1, local time, Bristol Myers Squibb announced that the U.S. Food and Drug Administration (FDA) has accepted its supplemental New Drug Application (sNDA) seeking approval for Camzyos (mavacamten) for the treatment of adolescent patients (aged 12 to under 18 years) with symptomatic obstructive hypertrophic cardiomyopathy (oHCM).<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">According to the press release, if approved, Camzyos would become the first cardiac myosin inhibitor (CMI) indicated for the treatment of adolescent patients with oHCM. The FDA has granted Priority Review for this application and has assigned a Prescription Drug User Fee Act (PDUFA) target action date of September 30, 2026. Previously, Camzyos has been approved for the treatment of adults with symptomatic oHCM (New York Heart Association [NYHA] functional class II-III) to improve functional capacity and symptoms.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Buy Camzyos (mavacamten)\u00a0online from China and save up to 80% on costs . no insurance needed . compare prices from a certified HongKong pharmacy .with fast shipping. Contact us now on WhatsApp to get the latest prices.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>On June 1, local time, Bristol Myers Squibb announced that the U.S. Food and Drug Administration (FDA) has accepted its supplemental New Drug Application (sNDA) seeking approval for Camzyos (mavacamten) for the treatment of adolescent patients (aged 12 to under 18 years) with symptomatic obstructive hypertrophic cardiomyopathy (oHCM). According to the press release, if approved, [&hellip;]<\/p>\n","protected":false},"author":3,"featured_media":2774,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[16],"tags":[],"class_list":["post-3870","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-news"],"blocksy_meta":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.6 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Bristol Myers Squibb: Camzyos mavacamten supplemental New Drug Application (sNDA) accepted by the U.S. FDA. - Xpharma China<\/title>\n<meta name=\"description\" content=\"Bristol Myers Squibb: Camzyos mavacamten supplemental New Drug Application (sNDA) accepted by the U.S. FDA. - Xpharma China\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/xpharma.com.cn\/index.php\/news\/bristol-myers-squibb-camzyos-mavacamten-supplemental-new-drug-application-snda-accepted-by-the-u-s-fda\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Bristol Myers Squibb: Camzyos mavacamten supplemental New Drug Application (sNDA) accepted by the U.S. FDA. - 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