{"id":21376,"date":"2023-08-22T09:13:00","date_gmt":"2023-08-22T09:13:00","guid":{"rendered":"https:\/\/www.prnasia.com\/story\/archive\/4189956_CN89956_0"},"modified":"2023-08-22T09:13:00","modified_gmt":"2023-08-22T09:13:00","slug":"kintor-pharma-announces-completion-of-patient-enrollment-in-phase-ii-clinical-trial-of-gt20029-for-treatment-of-androgenetic-alopecia-in-china","status":"publish","type":"post","link":"https:\/\/transmediavictoria.net.au\/?p=21376","title":{"rendered":"Kintor Pharma Announces Completion of Patient Enrollment in Phase II Clinical Trial of GT20029 for Treatment of Androgenetic Alopecia in China"},"content":{"rendered":"<p><span class=\"legendSpanClass\">SUZHOU, <span class=\"xn-location\">China<\/span><\/span>, <span class=\"legendSpanClass\"><span class=\"xn-chron\">Aug. 22, 2023<\/span><\/span> \/PRNewswire\/ &#8212;&nbsp;Kintor Pharmaceutical Limited (&#8220;Kintor Pharma&#8221;, HKEX: 9939), a clinical-stage biotechnology company developing innovative small molecules and biological therapeutics, announced that the company has completed the enrollment of 180 patients for the Phase II clinical trial of its in-house developed first-in-class proteolysis targeting chimera (PROTAC) compound GT20029 in <span class=\"xn-location\">China<\/span> for the treatment of male androgenetic alopecia (AGA). GT20029 was developed based on the in-house PROTAC platform and is the world&#8217;s first topical PROTAC compound which has entered the Phase II clinical stage.<\/p>\n<p>The Phase II clinical trial is a multi-center, randomized, double-blind, placebo-controlled study designed to evaluate the efficacy and safety of GT20029 for treating male AGA patients in <span class=\"xn-location\">China<\/span>, and to determine the recommended dosage for the Phase III clinical trial. This trial involves a total of 12 clinical research centers in <span class=\"xn-location\">China<\/span>, and Professor <span class=\"xn-person\">Yang Qinp<\/span><span id=\"spanHghlt9b24\">ing<\/span><span id=\"spanHghlted39\">&nbsp;fr<\/span>om Fudan University Huashan Hospital is the leading principal investigator (leading PI). The primary endpoint of&nbsp;this trial is the change from baseline in non-vellus target area hair counts (TAHC) after 12 weeks of treatment in comparison to placebo.<\/p>\n<p>Previously, Kintor Pharma has completed the Phase I clinical trials of GT20029 both in <span class=\"xn-location\">China<\/span> and the US, and the top-line data of more than 200 subjects has demonstrated that GT20029 has a good safety profile and is well-tolerated for single and multiple doses of topical application.<\/p>\n<p>Dr. <span class=\"xn-person\">Youzhi Tong<\/span>, founder, Chairman and Chief Executive Officer of Kintor Pharma, commented, &#8220;We would like to thank all the PIs from the centers and the company&#8217;s medical and clinical operation staffs for their joint efforts to finish the patients enrollment in the Phase II clinical trial of GT20029 in about four months. We expect to release the top-line data of the Phase II clinical trial in the first quarter of 2024, and look forward to collecting more efficacy and safety data of&nbsp;GT20029&nbsp;in this trial. &#8220;<\/p>\n<p>About Kintor Pharmaceutical Limited<\/p>\n<p>Kintor Pharmaceutical Limited is developing and commercializing a robust pipeline of innovative small molecule and biological therapeutics for oncology and androgen-receptor-related disease areas with unmet medical needs, including alopecia, acne, COVID-19, prostate cancer, liver and breast cancers. For more information, visit <a href=\"https:\/\/www.kintor.com.cn\/\" target=\"_blank\" rel=\"nofollow noopener\">www.kintor.com.cn<\/a>.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>SUZHOU, China, Aug. 22, 2023 \/PRNewswire\/ &#8212;&nbsp;Kintor Pharmaceutical Limited (&#8220;Kintor Pharma&#8221;, HKEX: 9939), a clinical-stage biotechnology company developing innovative small molecules and biological therapeutics, announced that the company has completed the enrollment of 180 patients for the Phase II clinical trial of its in-house developed first-in-class proteolysis targeting chimera (PROTAC) compound GT20029 in China for [&hellip;]<\/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-21376","post","type-post","status-publish","format-standard","hentry","category-business-news"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.9 - 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