{"id":11612,"date":"2023-11-13T23:18:00","date_gmt":"2023-11-13T15:18:00","guid":{"rendered":"https:\/\/flcube.com\/?p=11612"},"modified":"2024-11-06T23:25:18","modified_gmt":"2024-11-06T15:25:18","slug":"clinical-research-on-raav-gene-drug-zs805-for-fabry-disease-launched-by-zhishan-weixin","status":"publish","type":"post","link":"https:\/\/flcube.com\/?p=11612","title":{"rendered":"Clinical Research on rAAV Gene Drug ZS805 for Fabry Disease Launched by Zhishan Weixin"},"content":{"rendered":"\n<p>Zhishan Weixin Biotechnology Co., Ltd, a China-based biotech company, has announced the launch of the first clinical research project in China focused on a recombinant adeno-associated virus (rAAV) genetic therapy for the treatment of Fabry disease. The study will evaluate the adeno-associated virus vector ZS805 as a potential treatment across six tertiary hospitals in China.<\/p>\n\n\n\n<p><strong>ZS805: An Innovative Gene Drug<\/strong><br>ZS805 is an innovative Category 1 biologic and an rAAV gene drug independently developed by Zhishan Weixin, holding fully independent intellectual property rights. The molecule has been optimized through genetic engineering to ensure that the alpha-galactosidase-A protein is specifically expressed and efficiently secreted in liver cells. Zhishan Weixin has also selected AAV carrier serotypes that can cover the vast majority of patients, making ZS805 a potentially inclusive treatment option.<\/p>\n\n\n\n<p><strong>Understanding Fabry Disease<\/strong><br>Fabry disease, also known as alpha-galactosidase-A deficiency, is an inherited neurological disorder characterized by the enzyme alpha-galactosidase-A&#8217;s inability to efficiently break down lipids in the body. The mutated gene results in the buildup of lipids to harmful levels in the body&#8217;s autonomic nervous system, impacting breathing, cardiovascular function, as well as the eyes, and kidneys.<\/p>\n\n\n\n<p><strong>ZS805&#8217;s Potential Impact on Treatment<\/strong><br>Traditional treatment for Fabry disease involves enzyme replacement therapy, which requires patients to receive an infusion of agarase every two weeks for life. Zhishan Weixin\u2019s ZS805 is expected to provide a &#8220;one shot treatment&#8221; that could offer a durable and potential lifelong cure, revolutionizing the treatment landscape for Fabry disease.- <a href=\"https:\/\/flcube.com\">Flcube.com<\/a><\/p>\n\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Zhishan Weixin Biotechnology Co., Ltd, a China-based biotech company, has announced the launch of the&#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":[62,66,24,1959],"class_list":["post-11612","post","type-post","status-publish","format-standard","hentry","category-company","category-drug","tag-clinical-trial-approval-initiation","tag-gene-therapy","tag-rare-orphan-disease-drugs","tag-zhishan-weixin-biotechnology"],"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>Clinical Research on rAAV Gene Drug ZS805 for Fabry Disease Launched by Zhishan Weixin - Insight, China&#039;s Pharmaceutical Industry<\/title>\n<meta name=\"description\" content=\"Zhishan Weixin Biotechnology Co., Ltd, a China-based biotech company, has announced the launch of the first clinical research project in China focused on a recombinant adeno-associated virus (rAAV) genetic therapy for the treatment of Fabry disease. 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