{"id":27216,"date":"2022-08-01T23:32:00","date_gmt":"2022-08-01T15:32:00","guid":{"rendered":"https:\/\/flcube.com\/?p=27216"},"modified":"2025-02-17T23:35:38","modified_gmt":"2025-02-17T15:35:38","slug":"sanjin-pharmas-subsidiary-gets-fda-nod-for-bc007-cancer-drug-trial","status":"publish","type":"post","link":"https:\/\/flcube.com\/?p=27216","title":{"rendered":"Sanjin Pharma&#8217;s Subsidiary Gets FDA Nod for BC007 Cancer Drug Trial"},"content":{"rendered":"\n<p>China-based Guilin Sanjin Pharmaceutical Co. Ltd (<a href=\"https:\/\/www.google.com\/finance\/quote\/002275:SHE\">SHE: 002275<\/a>) announced that its subsidiary, Dragon Boat Pharmaceutical (Shanghai) Co., Ltd, has received approval from the U.S. Food and Drug Administration (FDA) to conduct a Phase I clinical study of BC007, a bispecific antibody (BsAb) targeting CLDN18.2 and CD47, in patients with solid tumors.<\/p>\n\n\n\n<p><strong>Drug Profile<\/strong><br>BC007 is designed with differential affinity for its two targets. The high affinity for CLDN18.2 enables specific binding to tumor cells expressing this antigen, while the lower affinity for CD47 enhances safety. The drug blocks the CD47\/SIRP\u03b1 signaling pathway, releasing CD47-mediated immunosuppression in tumors. No similar product is currently available globally.<\/p>\n\n\n\n<p><strong>Clinical Trial Details<\/strong><br>The Phase I study will assess the safety, tolerability, pharmacokinetics, immunogenicity, and preliminary antitumor efficacy of BC007 in solid tumor patients. The trial marks a key step in Dragon Boat&#8217;s efforts to develop innovative cancer therapies.<a href=\"https:\/\/flcube.com\/\">-Fineline Info &amp; Tech<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>China-based Guilin Sanjin Pharmaceutical Co. Ltd (SHE: 002275) announced that its subsidiary, Dragon Boat Pharmaceutical&#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":[16,3660,28,336,1169],"class_list":["post-27216","post","type-post","status-publish","format-standard","hentry","category-company","category-drug","tag-cancer","tag-dragon-boat-biopharmaceutical","tag-multi-specific-antibodies","tag-sanjin-pharmaceutical","tag-she-002275"],"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>Sanjin Pharma&#039;s Subsidiary Gets FDA Nod for BC007 Cancer Drug Trial - Insight, China&#039;s Pharmaceutical Industry<\/title>\n<meta name=\"description\" content=\"China-based Guilin Sanjin Pharmaceutical Co. Ltd (SHE: 002275) announced that its subsidiary, Dragon Boat Pharmaceutical (Shanghai) Co., Ltd, has received approval from the U.S. Food and Drug Administration (FDA) to conduct a Phase I clinical study of BC007, a bispecific antibody (BsAb) targeting CLDN18.2 and CD47, in patients with solid tumors.\" \/>\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=27216\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Sanjin Pharma&#039;s Subsidiary Gets FDA Nod for BC007 Cancer Drug Trial\" \/>\n<meta property=\"og:description\" content=\"Navigate the complexities of China\u2019s pharmaceutical industry with precision and clarity. FLCUBE delivers reliable data, news, and intelligence to broaden your horizons and sharpen your decision-making. 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