{"id":34806,"date":"2025-06-05T20:14:02","date_gmt":"2025-06-05T12:14:02","guid":{"rendered":"https:\/\/flcube.com\/?p=34806"},"modified":"2025-06-05T20:14:03","modified_gmt":"2025-06-05T12:14:03","slug":"innovent-biologics-ibi363-receives-breakthrough-therapy-designation-from-cde","status":"publish","type":"post","link":"https:\/\/flcube.com\/?p=34806","title":{"rendered":"Innovent Biologics&#8217; IBI363 Receives Breakthrough Therapy Designation from CDE"},"content":{"rendered":"\n<p>China-based Innovent Biologics, Inc. (<a href=\"https:\/\/www.google.com\/finance\/quote\/1801:HKG\">HKG: 1801<\/a>) announced that its first-in-class PD-1\/IL-2\u03b1-bias bispecific antibody (BsAb) fusion protein, IBI363, has received breakthrough therapy designation (BTD) from the Center for Drug Evaluation (CDE) in China. This designation is for the treatment of patients with locally advanced or metastatic squamous non-small cell lung cancer (sqNSCLC) that has progressed after platinum-based chemotherapy and anti-PD-1\/PD-L1 immunotherapy.<\/p>\n\n\n\n<p><strong>Clinical Data and Previous Designations<\/strong><br>IBI363 has demonstrated positive clinical data in treating patients with immune-resistant cold tumors, including non-small cell lung cancer, colorectal cancer, and melanoma. These results were presented at the 2025 American Society of Clinical Oncology (ASCO) Annual Meeting. Additionally, the drug previously received fast track designation from the US Food and Drug Administration (FDA) for use in melanoma.<a href=\"https:\/\/flcube.com\/\">-Fineline Info &amp; Tech<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>China-based Innovent Biologics, Inc. (HKG: 1801) announced that its first-in-class PD-1\/IL-2\u03b1-bias bispecific antibody (BsAb) fusion&#8230;<\/p>\n","protected":false},"author":1,"featured_media":34808,"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":[34,910,198,28],"class_list":["post-34806","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-company","category-drug","tag-breakthrough-therapy","tag-hkg-1801","tag-innovent-biologics","tag-multi-specific-antibodies"],"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>Innovent Biologics&#039; IBI363 Receives Breakthrough Therapy Designation from CDE - Insight, China&#039;s Pharmaceutical Industry<\/title>\n<meta name=\"description\" content=\"China-based Innovent Biologics, Inc. (HKG: 1801) announced that its first-in-class PD-1\/IL-2\u03b1-bias bispecific antibody (BsAb) fusion protein, IBI363, has received breakthrough therapy designation (BTD) from the Center for Drug Evaluation (CDE) in China. This designation is for the treatment of patients with locally advanced or metastatic squamous non-small cell lung cancer (sqNSCLC) that has progressed after platinum-based chemotherapy and anti-PD-1\/PD-L1 immunotherapy.\" \/>\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=34806\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Innovent Biologics&#039; IBI363 Receives Breakthrough Therapy Designation from CDE\" \/>\n<meta property=\"og:description\" content=\"China-based Innovent Biologics, Inc. (HKG: 1801) announced that its first-in-class PD-1\/IL-2\u03b1-bias bispecific antibody (BsAb) fusion protein, IBI363, has received breakthrough therapy designation (BTD) from the Center for Drug Evaluation (CDE) in China. 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