{"id":10970,"date":"2023-12-04T00:49:00","date_gmt":"2023-12-03T16:49:00","guid":{"rendered":"https:\/\/flcube.com\/?p=10970"},"modified":"2024-12-09T11:47:48","modified_gmt":"2024-12-09T03:47:48","slug":"akeso-biopharma-files-new-indication-for-penpulimab-in-first-line-npc-treatment","status":"publish","type":"post","link":"https:\/\/flcube.com\/?p=10970","title":{"rendered":"Akeso Biopharma Files New Indication for Penpulimab in First-Line NPC Treatment"},"content":{"rendered":"\n<p>Akeso Biopharma (<a href=\"https:\/\/www.google.com\/finance\/quote\/9926:HKG\">HKG: 9926<\/a>) has announced a new indication filing for its programmed death-1 (PD-1) inhibitor, penpulimab (AK105), seeking approval for its use in first-line treatment of recurrent or metastatic nasopharyngeal carcinoma (NPC) in combination with chemotherapy. The application is currently under review by China\u2019s Center for Drug Evaluation (CDE).<\/p>\n\n\n\n<p>Penpulimab was initially approved in August 2021 as a third-line treatment for relapsed\/refractory classic Hodgkin lymphoma (cHL). In January 2023, it received approval for first-line use in locally advanced or metastatic squamous non-small cell lung cancer (sq-NSCLC) in conjunction with chemotherapy. A regulatory decision is also pending for its application in the third-line setting for recurrent\/metastatic NPC in China.<\/p>\n\n\n\n<p>In December 2021, Akeso formed a 50-50 joint venture with Chia Tai Tianqing, granting exclusive marketing rights for penpulimab in China. Additionally, in April this year, Singapore-based Specialised Therapeutics Asia Pte Ltd secured an exclusive marketing license for penpulimab in Australia, Singapore, and Southeast Asia.- <a href=\"https:\/\/flcube.com\">Flcube.com<\/a><\/p>\n\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Akeso Biopharma (HKG: 9926) has announced a new indication filing for its programmed death-1 (PD-1)&#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":[360,16,661,2658,850,38,18],"class_list":["post-10970","post","type-post","status-publish","format-standard","hentry","category-company","category-drug","tag-akeso-biopharma","tag-cancer","tag-chia-tai-tianqing-pharmaceutical","tag-cttq-pharma","tag-hkg-9926","tag-market-approval-filings","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>Akeso Biopharma Files New Indication for Penpulimab in First-Line NPC Treatment - Insight, China&#039;s Pharmaceutical Industry<\/title>\n<meta name=\"description\" content=\"Akeso Biopharma (HKG: 9926) has announced a new indication filing for its programmed death-1 (PD-1) inhibitor, penpulimab (AK105), seeking approval for its use in first-line treatment of recurrent or metastatic nasopharyngeal carcinoma (NPC) in combination with chemotherapy. 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