{"id":18426,"date":"2024-12-17T14:07:46","date_gmt":"2024-12-17T06:07:46","guid":{"rendered":"https:\/\/flcube.com\/?p=18426"},"modified":"2024-12-17T14:07:48","modified_gmt":"2024-12-17T06:07:48","slug":"gsks-jemperli-receives-fda-breakthrough-therapy-designation-for-rectal-cancer-treatment","status":"publish","type":"post","link":"https:\/\/flcube.com\/?p=18426","title":{"rendered":"GSK&#8217;s Jemperli Receives FDA Breakthrough Therapy Designation for Rectal Cancer Treatment"},"content":{"rendered":"\n<p>UK-based pharmaceutical giant GSK (<a href=\"https:\/\/www.google.com\/finance\/quote\/GSK:NYSE\">NYSE: GSK<\/a>) has announced that it has received Breakthrough Therapy Designation (BTD) from the US Food and Drug Administration (FDA) for its drug Jemperli (dostarlimab). The designation is for the treatment of patients with locally advanced mismatch repair deficient (dMMR)\/microsatellite instability-high (MSI-H) rectal cancer.<\/p>\n\n\n\n<p><strong>Jemperli&#8217;s Background and Licensing History<\/strong><br>Jemperli, a programmed-death 1 (PD-1) monoclonal antibody (mAb), was discovered by AnaptysBio, Inc. and was licensed to TESARO, Inc., in a deal that took place in March 2014. Under the terms of that agreement, GSK is responsible for the ongoing research, development, commercialization, and manufacturing of both Jemperli and cobolimab (GSK4069889), a TIM-3 antagonist.<\/p>\n\n\n\n<p><strong>FDA Approval and Clinical Trial Results<\/strong><br>Jemperli gained FDA approval in July 2023 for use in combination with carboplatin and paclitaxel, followed by Jemperli as a single agent for the treatment of adult patients with primary advanced or recurrent endometrial cancer. In June 2024, GSK revealed results from a trial for Jemperli (dostarlimab-gxly) that demonstrated an unprecedented 100% clinical complete response (cCR) in patients with locally advanced rectal cancer.<a href=\"https:\/\/flcube.com\">-Fineline Info &amp; Tech<\/a><\/p>\n\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>UK-based pharmaceutical giant GSK (NYSE: GSK) has announced that it has received Breakthrough Therapy Designation&#8230;<\/p>\n","protected":false},"author":1,"featured_media":18427,"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":[34,16,184,914,18],"class_list":["post-18426","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-company","category-drug","tag-breakthrough-therapy","tag-cancer","tag-gsk","tag-nyse-gsk","tag-pd-1-l1"],"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>GSK&#039;s Jemperli Receives FDA Breakthrough Therapy Designation for Rectal Cancer Treatment - Insight, China&#039;s Pharmaceutical Industry<\/title>\n<meta name=\"description\" content=\"UK-based pharmaceutical giant GSK (NYSE: GSK) has announced that it has received Breakthrough Therapy Designation (BTD) from the US Food and Drug Administration (FDA) for its drug Jemperli (dostarlimab). The designation is for the treatment of patients with locally advanced mismatch repair deficient (dMMR)\/microsatellite instability-high (MSI-H) rectal cancer.\" \/>\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=18426\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"GSK&#039;s Jemperli Receives FDA Breakthrough Therapy Designation for Rectal Cancer Treatment\" \/>\n<meta property=\"og:description\" content=\"UK-based pharmaceutical giant GSK (NYSE: GSK) has announced that it has received Breakthrough Therapy Designation (BTD) from the US Food and Drug Administration (FDA) for its drug Jemperli (dostarlimab). The designation is for the treatment of patients with locally advanced mismatch repair deficient (dMMR)\/microsatellite instability-high (MSI-H) rectal cancer.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/flcube.com\/?p=18426\" \/>\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=\"2024-12-17T06:07:46+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2024-12-17T06:07:48+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/flcube.com\/wp-content\/uploads\/2024\/12\/1707.png\" \/>\n\t<meta property=\"og:image:width\" content=\"1080\" \/>\n\t<meta property=\"og:image:height\" content=\"566\" \/>\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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