{"id":16068,"date":"2023-07-18T16:11:00","date_gmt":"2023-07-18T08:11:00","guid":{"rendered":"https:\/\/flcube.com\/?p=16068"},"modified":"2024-12-01T16:13:27","modified_gmt":"2024-12-01T08:13:27","slug":"janssens-rybrevant-meets-primary-endpoint-in-phase-iii-nsclc-study","status":"publish","type":"post","link":"https:\/\/flcube.com\/?p=16068","title":{"rendered":"Janssen&#8217;s Rybrevant Meets Primary Endpoint in Phase III NSCLC Study"},"content":{"rendered":"\n<p>The Janssen unit of Johnson &amp; Johnson (J&amp;J; <a href=\"https:\/\/www.google.com\/finance\/quote\/JNJ:NYSE\">NYSE: JNJ<\/a>) has announced positive results from a Phase III confirmatory study for the bispecific antibody Rybrevant (amivantamab). The study focused on patients with newly diagnosed advanced or metastatic non-small cell lung cancer (NSCLC) that harbor epidermal growth factor receptor (EGFR) exon 20 insertion mutations. According to the press release, the trial successfully met its primary endpoint of significantly improving progression-free survival (PFS), with a safety profile consistent with the individual medicines used.<\/p>\n\n\n\n<p><strong>Reinforcing Accelerated Approval and Ongoing Trials<\/strong><br>These encouraging results further support the accelerated approval granted to Rybrevant in the US in 2021. The biologic is currently the subject of several combination trials with other molecules for the treatment of NSCLC, indicating the potential for expanded use and improved outcomes in lung cancer treatment.<a href=\"https:\/\/flcube.com\">-Fineline Info &amp; Tech<\/a><\/p>\n\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>The Janssen unit of Johnson &amp; Johnson (J&amp;J; NYSE: JNJ) has announced positive results from&#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":[16,17,150,149,28,858],"class_list":["post-16068","post","type-post","status-publish","format-standard","hentry","category-company","category-drug","tag-cancer","tag-clinical-trial-results","tag-jj","tag-johnson-johnson","tag-multi-specific-antibodies","tag-nyse-jnj"],"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>Janssen&#039;s Rybrevant Meets Primary Endpoint in Phase III NSCLC Study - Insight, China&#039;s Pharmaceutical Industry<\/title>\n<meta name=\"description\" content=\"The Janssen unit of Johnson &amp; Johnson (J&amp;J; NYSE: JNJ) has announced positive results from a Phase III confirmatory study for the bispecific antibody Rybrevant (amivantamab). The study focused on patients with newly diagnosed advanced or metastatic non-small cell lung cancer (NSCLC) that harbor epidermal growth factor receptor (EGFR) exon 20 insertion mutations. According to the press release, the trial successfully met its primary endpoint of significantly improving progression-free survival (PFS), with a safety profile consistent with the individual medicines used.\" \/>\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=16068\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Janssen&#039;s Rybrevant Meets Primary Endpoint in Phase III NSCLC Study\" \/>\n<meta property=\"og:description\" content=\"Navigate the complexities of China\u2019s pharmaceutical industry with precision and clarity. 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