{"id":18347,"date":"2023-05-06T12:00:00","date_gmt":"2023-05-06T12:00:00","guid":{"rendered":"https:\/\/www.prnasia.com\/story\/archive\/4091661_CN91661_0"},"modified":"2023-05-06T12:00:00","modified_gmt":"2023-05-06T12:00:00","slug":"suzhougenassist-therapeutic-co-ltd-recently-announced-that-its-first-base-editing-product-gen6050-has-submitted-a-pre-ind-application-to-the-fda-and-has-been-accepted","status":"publish","type":"post","link":"https:\/\/transmediavictoria.net.au\/?p=18347","title":{"rendered":"SuzhouGenAssist Therapeutic Co.,Ltd recently announced that its first base editing product, GEN6050, has submitted a pre-IND application to the FDA and has been accepted"},"content":{"rendered":"

SUZHOU, China<\/span><\/span>, May 6, 2023<\/span><\/span> \/PRNewswire\/ — Suzhou<\/span> GenAssist Therapeutic Co.,Ltd recently announced its pre-IND application of their first base editing product, GEN6050 and the acceptance by the FDA.<\/p>\n

GEN6050 is an in vivo<\/i> base editing drug that targets exon 50 skipping in the Duchenne muscular dystrophy (DMD) gene. It is designed to restore the expression of dystrophin protein by base editing.<\/p>\n

DMD is a rare disease with a high incidence rate, with one DMD patient diagnosed per 4000 newborn boys. According to LEIDEN DMD data, exon 50 skipping can be used to treat 4% of DMD patients with large deletions [1]<\/sup>. Nowadays, DMD patients are often treated with marketed drugs such as glucocorticoids and ASOs, which target exon skipping at exon 45, 51, and 53. Until now, there is no approved drug targeting exon 50 skipping in the dystrophin gene, even in clinical stage. In addition, no AAV-delivered<\/span><\/i><\/b> <\/span>in<\/span> vivo<\/b><\/i> base editing<\/b> drugs for any other indication have entered clinical trials globally. As one of the pioneering companies developing in vivo<\/i> base editing drugs, Suzhou <\/span>GenAssist Therapeutic has already established a comprehensive evaluation system for base editing drugs. Moreover, the Company is developing base editing products for more DMD mutations.<\/p>\n

The Pre-IND meeting usually refers to a voluntary meeting where the sponsor submits and communicates with the regulatory authority before conducting clinical trials of investigational new drugs (IND). The main purpose of the meeting is to review pharmacological study and non-clinical study, and to discuss whether existing research results are sufficient to support clinical research.<\/p>\n

About Suzhou GenAssist Therapeutic<\/b><\/p>\n

Suzhou GenAssist Therapeutic is a globally leading innovative company founded in July 2020<\/span>. The headquarter of Suzhou GenAssist Therapeutic locates in Suzhou, China<\/span>, with subsidiaries in Shanghai, China<\/span> and Boston<\/span>, USA<\/span>. Suzhou GenAssist owns the global rights of TAM base editor, which is licensed from Chinese Academy of Nutrition and Health and Westlake University. Suzhou GenAssist Therapeutic is devoted to transform cutting-edging science into products that bring significant benefits to patients. For more information, please visit www.genassisttx.com<\/a><\/span>.<\/p>\n

[1] Data Source: Leiden Duchenne Muscular Dystrophy pages (version March 11, 2008<\/span>).<\/p>\n","protected":false},"excerpt":{"rendered":"

SUZHOU, China, May 6, 2023 \/PRNewswire\/ — Suzhou GenAssist Therapeutic Co.,Ltd recently announced its pre-IND application of their first base editing product, GEN6050 and the acceptance by the FDA. GEN6050 is an in vivo base editing drug that targets exon 50 skipping in the Duchenne muscular dystrophy (DMD) gene. It is designed to restore the expression […]<\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[20],"tags":[],"class_list":["post-18347","post","type-post","status-publish","format-standard","hentry","category-business-news"],"yoast_head":"\nSuzhouGenAssist Therapeutic Co.,Ltd recently announced that its first base editing product, GEN6050, has submitted a pre-IND application to the FDA and has been accepted - My Blog<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/transmediavictoria.net.au\/?p=18347\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"SuzhouGenAssist Therapeutic Co.,Ltd recently announced that its first base editing product, GEN6050, has submitted a pre-IND application to the FDA and has been accepted - My Blog\" \/>\n<meta property=\"og:description\" content=\"SUZHOU, China, May 6, 2023 \/PRNewswire\/ — Suzhou GenAssist Therapeutic Co.,Ltd recently announced its pre-IND application of their first base editing product, GEN6050 and the acceptance by the FDA. 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