{"id":35380,"date":"2025-06-17T15:36:07","date_gmt":"2025-06-17T07:36:07","guid":{"rendered":"https:\/\/flcube.com\/?p=35380"},"modified":"2025-06-17T15:36:07","modified_gmt":"2025-06-17T07:36:07","slug":"abbvies-venclexta-fails-to-meet-overall-survival-endpoint-in-hr-mds-trial","status":"publish","type":"post","link":"https:\/\/flcube.com\/?p=35380","title":{"rendered":"AbbVie&#8217;s Venclexta Fails to Meet Overall Survival Endpoint in HR-MDS Trial"},"content":{"rendered":"\n<p>US-based major AbbVie Inc., (<a href=\"https:\/\/www.google.com\/finance\/quote\/ABBV:NYSE\">NYSE: ABBV<\/a>) has revealed disappointing data for its Venclexta (venetoclax) in combination with azacitidine in newly diagnosed higher-risk myelodysplastic syndrome (HR-MDS). The first-in-class BCL-2 inhibitor failed to meet the primary endpoint of overall survival (OS) in the global Phase III VERONA study, although no new safety signals were observed.<\/p>\n\n\n\n<p><strong>Study Details<\/strong><\/p>\n\n\n\n<p>The VERONA study compared the efficacy and safety of the venetoclax\/azacitidine combination against azacitidine plus placebo. Despite the setback, AbbVie and Roche, who co-developed Venclexta\/Venclyxto, remain committed to advancing BCL-2 research. The therapy is jointly commercialized in the US by AbbVie and Genentech (a Roche Group company), with AbbVie leading ex-US commercialization.<\/p>\n\n\n\n<p><strong>Global Authorization and Ongoing Research<\/strong><\/p>\n\n\n\n<p>Venetoclax is currently approved in over 80 countries, including the US, and holds marketing authorization under dual brand names in different regions. The partners continue ongoing clinical investigations of venetoclax across multiple hematologic malignancies and solid tumors.<a href=\"https:\/\/flcube.com\/\">-Fineline Info &amp; Tech<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>US-based major AbbVie Inc., (NYSE: ABBV) has revealed disappointing data for its Venclexta (venetoclax) in&#8230;<\/p>\n","protected":false},"author":1,"featured_media":35381,"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":[234,17,853],"class_list":["post-35380","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-company","category-drug","tag-abbvie","tag-clinical-trial-results","tag-nyse-abbv"],"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>AbbVie&#039;s Venclexta Fails to Meet Overall Survival Endpoint in HR-MDS Trial - Insight, China&#039;s Pharmaceutical Industry<\/title>\n<meta name=\"description\" content=\"US-based major AbbVie Inc., (NYSE: ABBV) has revealed disappointing data for its Venclexta (venetoclax) in combination with azacitidine in newly diagnosed higher-risk myelodysplastic syndrome (HR-MDS). 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