{"id":12209,"date":"2023-10-31T10:33:00","date_gmt":"2023-10-31T02:33:00","guid":{"rendered":"https:\/\/flcube.com\/?p=12209"},"modified":"2024-11-12T10:40:04","modified_gmt":"2024-11-12T02:40:04","slug":"cspc-pharmaceutical-group-gains-nmpa-approval-for-bivalent-covid-19-mrna-vaccine-study","status":"publish","type":"post","link":"https:\/\/flcube.com\/?p=12209","title":{"rendered":"CSPC Pharmaceutical Group Gains NMPA Approval for Bivalent COVID-19 mRNA Vaccine Study"},"content":{"rendered":"\n<p>CSPC Pharmaceutical Group Ltd (<a href=\"https:\/\/www.google.com\/finance\/quote\/1093:HKG\">HKG: 1093<\/a>), a prominent pharmaceutical company based in China, has announced that it has received approval from the National Medical Products Administration (NMPA) to conduct a clinical study for its bivalent COVID-19 mRNA vaccine SYS6006.32, targeting the XBB.1.5 and BQ.1 variants.<\/p>\n\n\n\n<p><strong>Vaccine Development and Immunogenicity<\/strong><br>SYS6006.32 is developed based on CSPC\u2019s first-generation COVID-19 mRNA vaccine, DuEnTai. Non-clinical research data indicates that SYS6006.32 exhibits very high immunogenicity against mainstream variants such as EG.5 and XBB.1.5, with live virus neutralizing antibody levels 108 and 88 times higher than those observed with DuEnTai, respectively.<\/p>\n\n\n\n<p><strong>Broad-Spectrum Immune Activity and Safety Profile<\/strong><br>In addition to its high efficacy against specific variants, SYS6006.32 also demonstrates broad-spectrum cross-immune activity against a range of variants, including XBB.1.16, XBB.1.9, BA.5, BQ.1, and BA.2.86. Regarding safety, the vaccine does not introduce any new risks compared to its predecessor, DuEnTai, ensuring a favorable safety profile for the new bivalent formulation.<a href=\"https:\/\/flcube.com\">-Fineline Info &amp; Tech<\/a><\/p>\n\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>CSPC Pharmaceutical Group Ltd (HKG: 1093), a prominent pharmaceutical company based in China, has announced&#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":[62,13,171,855,12],"class_list":["post-12209","post","type-post","status-publish","format-standard","hentry","category-company","category-drug","tag-clinical-trial-approval-initiation","tag-covid-19","tag-cspc-pharmaceutical","tag-hkg-1093","tag-vaccine"],"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>CSPC Pharmaceutical Group Gains NMPA Approval for Bivalent COVID-19 mRNA Vaccine Study - Insight, China&#039;s Pharmaceutical Industry<\/title>\n<meta name=\"description\" content=\"CSPC Pharmaceutical Group Ltd (HKG: 1093), a prominent pharmaceutical company based in China, has announced that it has received approval from the National Medical Products Administration (NMPA) to conduct a clinical study for its bivalent COVID-19 mRNA vaccine SYS6006.32, targeting the XBB.1.5 and BQ.1 variants.\" \/>\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=12209\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"CSPC Pharmaceutical Group Gains NMPA Approval for Bivalent COVID-19 mRNA Vaccine Study\" \/>\n<meta property=\"og:description\" content=\"Navigate the complexities of China\u2019s pharmaceutical industry with precision and clarity. 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