{"id":31218,"date":"2025-04-03T18:06:35","date_gmt":"2025-04-03T10:06:35","guid":{"rendered":"https:\/\/flcube.com\/?p=31218"},"modified":"2025-04-03T18:06:36","modified_gmt":"2025-04-03T10:06:36","slug":"novartis-vanrafia-gets-fda-accelerated-approval-for-igan","status":"publish","type":"post","link":"https:\/\/flcube.com\/?p=31218","title":{"rendered":"Novartis&#8217; Vanrafia Gets FDA Accelerated Approval for IgAN"},"content":{"rendered":"\n<p>Switzerland-based Novartis (<a href=\"https:\/\/www.google.com\/finance\/quote\/NVS:NYSE\">NYSE: NVS<\/a>) announced that it has received accelerated approval from the US Food and Drug Administration (FDA) for Vanrafia (atrasentan). This endothelin A (ETA) receptor antagonist is now approved to reduce proteinuria in adults with primary immunoglobulin A nephropathy (IgAN) at risk of rapid disease progression.<\/p>\n\n\n\n<p><strong>Clinical Trial Results<\/strong><br>The approval is based on interim results from the Phase III ALIGN study, which demonstrated a significant reduction in proteinuria at 36 weeks compared to placebo. While the study confirmed the drug&#8217;s effect on proteinuria, it remains to be established whether Vanrafia slows the decline in kidney function in patients with IgAN.<\/p>\n\n\n\n<p><strong>Acquisition Background<\/strong><br>Vanrafia was acquired by Novartis through its USD 3.5 billion acquisition of Chinook Therapeutics, a US-based kidney disease specialist, in 2023. This strategic move underscores Novartis&#8217;s commitment to expanding its portfolio in nephrology.<a href=\"https:\/\/flcube.com\/\">-Fineline Info &amp; Tech<\/a><\/p>\n\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Switzerland-based Novartis (NYSE: NVS) announced that it has received accelerated approval from the US Food&#8230;<\/p>\n","protected":false},"author":1,"featured_media":31219,"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":true,"jetpack_social_options":{"image_generator_settings":{"template":"highway","default_image_id":0,"font":"","enabled":false},"version":2}},"categories":[7,11],"tags":[65,2405,140,865,15],"class_list":["post-31218","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-company","category-drug","tag-auto-immune","tag-chinook-therapeutics","tag-novartis","tag-nyse-nvs","tag-product-approvals"],"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>Novartis&#039; Vanrafia Gets FDA Accelerated Approval for IgAN - Insight, China&#039;s Pharmaceutical Industry<\/title>\n<meta name=\"description\" content=\"Switzerland-based Novartis (NYSE: NVS) announced that it has received accelerated approval from the US Food and Drug Administration (FDA) for Vanrafia (atrasentan). This endothelin A (ETA) receptor antagonist is now approved to reduce proteinuria in adults with primary immunoglobulin A nephropathy (IgAN) at risk of rapid disease progression.\" \/>\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=31218\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Novartis&#039; Vanrafia Gets FDA Accelerated Approval for IgAN\" \/>\n<meta property=\"og:description\" content=\"Switzerland-based Novartis (NYSE: NVS) announced that it has received accelerated approval from the US Food and Drug Administration (FDA) for Vanrafia (atrasentan). This endothelin A (ETA) receptor antagonist is now approved to reduce proteinuria in adults with primary immunoglobulin A nephropathy (IgAN) at risk of rapid disease progression.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/flcube.com\/?p=31218\" \/>\n<meta property=\"og:site_name\" content=\"Insight, China&#039;s Pharmaceutical Industry\" \/>\n<meta property=\"article:publisher\" content=\"https:\/\/www.facebook.com\/profile.php?id=61566606313834\" \/>\n<meta property=\"article:published_time\" content=\"2025-04-03T10:06:35+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2025-04-03T10:06:36+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/flcube.com\/wp-content\/uploads\/2025\/04\/0313-png.webp\" \/>\n\t<meta property=\"og:image:width\" content=\"1080\" \/>\n\t<meta property=\"og:image:height\" content=\"608\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/png\" \/>\n<meta name=\"author\" content=\"Fineline Cube\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:description\" content=\"Navigate the complexities of China\u2019s pharmaceutical industry with precision and clarity. 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