{"id":34109,"date":"2025-05-26T12:28:58","date_gmt":"2025-05-26T04:28:58","guid":{"rendered":"https:\/\/flcube.com\/?p=34109"},"modified":"2025-05-26T12:28:59","modified_gmt":"2025-05-26T04:28:59","slug":"roches-itovebi-recommended-for-eu-approval-in-pik3ca-mutated-breast-cancer","status":"publish","type":"post","link":"https:\/\/flcube.com\/?p=34109","title":{"rendered":"Roche&#8217;s Itovebi Recommended for EU Approval in PIK3CA-Mutated Breast Cancer"},"content":{"rendered":"\n<p>Swiss giant Roche AG (<a href=\"https:\/\/www.google.com\/finance\/quote\/ROG:SWX\">SWX: ROG<\/a>, <a href=\"https:\/\/www.google.com\/finance\/quote\/RHHBY:OTCMKTS\">OTCMKTS: RHHBY<\/a>) announced that its Itovebi (inavolisib) has been recommended for market approval by the European Medicines Agency&#8217;s Medicinal Products for Human Use (CHMP). The recommendation supports the use of Itovebi in combination with palbociclib and fulvestrant for adult patients with PIK3CA-mutated, oestrogen receptor (ER)-positive, human epidermal growth factor receptor 2 (HER2)-negative, locally advanced or metastatic breast cancer, following recurrence on or within 12 months of completing adjuvant endocrine treatment.<\/p>\n\n\n\n<p><strong>Clinical Trial Results<\/strong><br>The recommendation is based on results from the phase III INAVO120 study, which demonstrated a 57% reduction in the risk of disease worsening or death (progression-free survival [PFS]) with the Itovebi-based regimen compared to palbociclib and fulvestrant alone (15.0 months vs. 7.3 months) in the first-line setting. Additionally, the Itovebi-based regimen was well tolerated, with no new safety signals observed.<a href=\"https:\/\/flcube.com\/\">-Fineline Info &amp; Tech<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Swiss giant Roche AG (SWX: ROG, OTCMKTS: RHHBY) announced that its Itovebi (inavolisib) has been&#8230;<\/p>\n","protected":false},"author":1,"featured_media":34110,"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":[16,940,163,939],"class_list":["post-34109","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-company","category-drug","tag-cancer","tag-otcmkts-rhhby","tag-roche","tag-swx-rop"],"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>Roche&#039;s Itovebi Recommended for EU Approval in PIK3CA-Mutated Breast Cancer - Insight, China&#039;s Pharmaceutical Industry<\/title>\n<meta name=\"description\" content=\"Swiss giant Roche AG (SWX: ROG, OTCMKTS: RHHBY) announced that its Itovebi (inavolisib) has been recommended for market approval by the European Medicines Agency&#039;s Medicinal Products for Human Use (CHMP). The recommendation supports the use of Itovebi in combination with palbociclib and fulvestrant for adult patients with PIK3CA-mutated, oestrogen receptor (ER)-positive, human epidermal growth factor receptor 2 (HER2)-negative, locally advanced or metastatic breast cancer, following recurrence on or within 12 months of completing adjuvant endocrine treatment.\" \/>\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=34109\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Roche&#039;s Itovebi Recommended for EU Approval in PIK3CA-Mutated Breast Cancer\" \/>\n<meta property=\"og:description\" content=\"Swiss giant Roche AG (SWX: ROG, OTCMKTS: RHHBY) announced that its Itovebi (inavolisib) has been recommended for market approval by the European Medicines Agency&#039;s Medicinal Products for Human Use (CHMP). The recommendation supports the use of Itovebi in combination with palbociclib and fulvestrant for adult patients with PIK3CA-mutated, oestrogen receptor (ER)-positive, human epidermal growth factor receptor 2 (HER2)-negative, locally advanced or metastatic breast cancer, following recurrence on or within 12 months of completing adjuvant endocrine treatment.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/flcube.com\/?p=34109\" \/>\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=\"2025-05-26T04:28:58+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2025-05-26T04:28:59+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/flcube.com\/wp-content\/uploads\/2025\/05\/2606.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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