{"id":1053,"date":"2024-09-18T14:20:15","date_gmt":"2024-09-18T06:20:15","guid":{"rendered":"https:\/\/flcube.com\/?p=1053"},"modified":"2024-11-23T21:47:08","modified_gmt":"2024-11-23T13:47:08","slug":"mercks-keytruda-gains-expanded-approval-for-first-line-melanoma-treatment-in-china","status":"publish","type":"post","link":"https:\/\/flcube.com\/?p=1053","title":{"rendered":"Merck&#8217;s Keytruda Gains Expanded Approval for First-Line Melanoma Treatment in China"},"content":{"rendered":"\n<p>Merck &amp; Co., Inc. (<a href=\"https:\/\/www.google.com\/finance\/quote\/MRK:NYSE\">NYSE: MRK<\/a>), a leading US pharmaceutical company, has announced that its programmed death-1 (PD-1) inhibitor, Keytruda (pembrolizumab), has received expanded approval in China. The updated approval allows the drug&#8217;s package insert to be revised to include &#8220;pembrolizumab is suitable for the treatment of unresectable or metastatic melanoma,&#8221; broadening its use beyond the previous indication of &#8220;pembrolizumab is suitable for the treatment of unresectable or metastatic melanoma that has failed first-line therapy.&#8221;<\/p>\n\n\n\n<p>Since its initial approval in China in 2018 for second-line advanced melanoma, Keytruda has now become the first and only PD-1 inhibitor approved for first-line melanoma treatment in the country. The drug has accumulated a dozen indications in China, spanning a range of cancers including melanoma, non-small cell lung cancer, esophageal squamous cell carcinoma, head and neck squamous cell carcinoma, colorectal cancer, hepatocellular carcinoma, triple negative breast cancer, MSI-H\/dMMR solid tumor, gastric cancer, bile duct cancer, and others.  <a href=\"https:\/\/flcube.com\">-Fineline Info &amp; Tech<\/a><\/p>\n\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Merck &amp; Co., Inc. (NYSE: MRK), a leading US pharmaceutical company, has announced that its&#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":[120,903,18,15],"class_list":["post-1053","post","type-post","status-publish","format-standard","hentry","category-company","category-drug","tag-merck","tag-nyse-mrk","tag-pd-1-l1","tag-product-approvals"],"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>Merck&#039;s Keytruda Gains Expanded Approval for First-Line Melanoma Treatment in China - Insight, China&#039;s Pharmaceutical Industry<\/title>\n<meta name=\"description\" content=\"Merck &amp; Co., Inc. (NYSE: MRK), a leading US pharmaceutical company, has announced that its programmed death-1 (PD-1) inhibitor, Keytruda (pembrolizumab), has received expanded approval in China. 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