{"id":41828,"date":"2025-11-30T10:15:00","date_gmt":"2025-11-30T10:15:00","guid":{"rendered":"https:\/\/www.prnasia.com\/story\/archive\/4835459_AE35459_0"},"modified":"2025-11-30T10:15:00","modified_gmt":"2025-11-30T10:15:00","slug":"ascletis-selects-its-first-oral-glp-1r-gipr-gcgr-triple-peptide-agonist-asc37-for-clinical-development","status":"publish","type":"post","link":"https:\/\/transmediavictoria.net.au\/?p=41828","title":{"rendered":"Ascletis Selects Its First Oral GLP-1R\/GIPR\/GCGR Triple Peptide Agonist, ASC37, for Clinical Development"},"content":{"rendered":"<div id=\"dvContent\" readability=\"157.22292284866\">\n<p>&#8211;&nbsp; <i>Utilizing Ascletis&#8217; Peptide Oral Transport ENhancement Technology (POTENT), ASC37 oral tablets achieved average absolute oral bioavailability of 4.2%, approximately 9<\/i><i>&#8211;<\/i><i>, 30<\/i><i>&#8211;<\/i><i>, <\/i><i>and <\/i><i>60-fold higher than semaglutide, tirzepatide, and retatrutide<\/i> <i>in the oral SNAC formulation, respectively, in head-to-head non-human primate (NHP) studies.<\/i><\/p>\n<p>&#8211;&nbsp; <i>ASC37 oral tablets&#8217; drug exposure, as measured by the <\/i><i>a<\/i><i>rea <\/i><i>u<\/i><i>nder <\/i><i>c<\/i><i>urve<\/i><i> (<\/i><i>AUC<\/i><i>),<\/i><i> was approximately 57-fold of retatrutide&#8217;s drug exposure in head-to-head NHP studies<\/i><i>.<\/i><\/p>\n<p>&#8211;&nbsp; <i>Average observed half-life of ASC37 oral tablets was approximately 56 hours in NHP studies, supporting once daily and less frequent oral dosing. <\/i><\/p>\n<p>&#8211;&nbsp; <i>ASC37 in vitro activity was approximately 5-, 4- and 4-fold more potent than retatrutide for GLP-1R, GIPR and GCGR, respectively.<\/i><\/p>\n<p>&#8211;&nbsp; <i>Submission of an Investigational New Drug Application (IND) to the U.S. Food and Drug Administration (FDA) for ASC37 oral tablets is expected in the second quarter of 2026.<\/i><\/p>\n<p>&#8211;&nbsp; <i>The Company will host a conference call in Mandarin at <span class=\"xn-chron\">10:00 a.m.<\/span> China Standard Time on <span class=\"xn-chron\">December 1, 2025<\/span>. <\/i><\/p>\n<p><span class=\"legendSpanClass\"><span class=\"xn-location\">HONG KONG<\/span><\/span>, <span class=\"legendSpanClass\"><span class=\"xn-chron\">Nov. 30, 2025<\/span><\/span> \/PRNewswire\/ &#8212; Ascletis Pharma Inc. (HKEX: 1672, &#8220;Ascletis&#8221;) announces that it has selected ASC37 oral tablets, its first oral GLP-1R\/GIPR\/GCGR<sup>[1]<\/sup> triple peptide agonist, as a clinical development candidate. Ascletis expects to submit an Investigational New Drug Application (IND)&nbsp;to the U.S. Food and Drug Administration&nbsp;(FDA) for ASC37 oral tablets for the treatment of obesity&nbsp;in the second quarter of 2026.<\/p>\n<p>ASC37 oral tablets is the Company&#8217;s first incretin drug candidate developed with its proprietary Peptide Oral Transport ENhancement Technology (POTENT).&nbsp;<\/p>\n<p>ASC37, a GLP-1R, GIPR, and GCGR&nbsp;triple peptide agonist, was discovered and optimized in-house utilizing Ascletis&#8217;&nbsp;Artificial Intelligence-Assisted Structure-Based Drug Discovery (AISBDD). ASC37 <i>in vitro<\/i> activity was approximately 5-, 4-, and 4-fold more potent than retatrutide for GLP-1R, GIPR and GCGR, respectively.<\/p>\n<p>Utilizing Ascletis&#8217; POTENT technology, ASC37 oral tablets achieved average absolute oral bioavailability<sup>[2]<\/sup> of 4.2%, which was approximately 9-, 30-, and 60-fold higher than semaglutide, tirzepatide, and retatrutide in the oral SNAC<sup> [3]<\/sup> formulation, respectively, in head-to-head non-human primate (NHP) studies. Furthermore, after oral administration, ASC37 oral tablets&#8217; drug exposure, as measured by the area under curve (AUC), with the POTENT formulation was approximately&nbsp;57-fold of retatrutide&#8217;s drug exposure with the oral SNAC formulation, in head-to-head NHP studies.<\/p>\n<p>Average observed half-life of ASC37 oral tablets was approximately 56 hours in NHP&nbsp;studies, supporting once daily and less frequent oral dosing.<\/p>\n<p>&nbsp;&#8220;Selection of ASC37, a promising oral GLP-1R\/GIPR\/GCGR triple peptide agonist, for clinical development once again demonstrates our strong R&amp;D capabilities and our commitment to address the unmet needs for the treatment of obesity,&#8221; said <span class=\"xn-person\">Jinzi Jason Wu<\/span>, Ph.D., Founder, Chairman and CEO of Ascletis, &#8220;Leveraging our proprietary technology platforms, including AISBDD&nbsp;and POTENT, Ascletis has successfully established a highly competitive, differentiated and diverse pipeline portfolio which can potentially effectively address the various treatment needs of patients with obesity and other metabolic diseases.&#8221;<\/p>\n<div>\n<table border=\"0\" cellspacing=\"0\" cellpadding=\"1\" class=\"prnbcc\">\n<tbody readability=\"4\">\n<tr readability=\"13.5\">\n<td class=\"prnpr2 prnpl2 prnvab prnsbtb0 prnrbrb0 prnsbbb0 prnsblb0\" colspan=\"1\" rowspan=\"1\" readability=\"14\">\n<p class=\"prnml4\"><span class=\"prnews_span\"><sup>[1] <\/sup>GLP-1R: glucagon-like peptide 1 receptor, GIPR: gastric inhibitory polypeptide receptor, GCGR: glucagon receptor<\/span><\/p>\n<p class=\"prnml4\"><span class=\"prnews_span\"><sup>[2]&nbsp;<\/sup>absolute oral bioavailability: the percentage of an orally administered drug that reaches the systemic circulation (bloodstream), compared to an intravenous (IV) dose of the same drug<\/span><\/p>\n<p class=\"prnml4\"><span class=\"prnews_span\"><sup>[3] <\/sup>SNAC: Salcaprozate&nbsp;Sodium<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table><\/div>\n<p><b>Conference Call<\/b><\/p>\n<p>Ascletis will host a conference call&nbsp;in Mandarin at 10:00 a.m.&nbsp;China&nbsp;Standard Time&nbsp;on <span class=\"xn-chron\">December 1, 2025<\/span>. A live webcast of the call will be&nbsp;available via <span class=\"xn-money\">Tencent<\/span> Meeting\/ VooV Meeting, with the Meeting ID: 495-266-842, or access links of:<\/p>\n<p>Chinese Mainland:<a href=\"https:\/\/meeting.tencent.com\/dm\/10ve6whW8Rbl\" target=\"_blank\" rel=\"nofollow noopener\">&nbsp;https:\/\/meeting.<span class=\"xn-money\">tencent<\/span>.com\/dm\/10ve6whW8Rbl<\/a>; or<\/p>\n<p>International: <a href=\"https:\/\/voovmeeting.com\/dm\/10ve6whW8Rbl\" target=\"_blank\" rel=\"nofollow noopener\">https:\/\/voovmeeting.com\/dm\/10ve6whW8Rbl<\/a>.<\/p>\n<p><b>About Ascletis Pharma Inc.<\/b><\/p>\n<p>Ascletis Pharma Inc. is a fully integrated biotechnology company focused on the development and commercialization of potential best-in-class and first-in-class therapeutics to treat metabolic diseases. Utilizing its proprietary Artificial Intelligence-Assisted Structure-Based Drug Discovery (AISBDD) and Ultra-Long-Acting Platform (ULAP) technologies as well as Peptide Oral Transport ENhancement Technology (POTENT), Ascletis has developed multiple drug candidates in-house, including both small molecules and peptides, such as its lead program, ASC30, a small molecule GLP-1R agonist designed to be administered once daily orally and once monthly to once quarterly subcutaneously as a treatment therapy and a maintenance therapy for chronic weight management; ASC36, a once-monthly subcutaneously administered amylin receptor peptide agonist, ASC35,&nbsp;a once-monthly subcutaneously administered GLP-1R\/GIPR dual peptide agonist and ASC37, an oral GLP-1R\/GIPR\/GCGR triple peptide agonist for chronic weight management. Ascletis is listed on the Hong Kong Stock Exchange (1672.HK).<\/p>\n<p>For more information, please visit <a href=\"http:\/\/www.ascletis.com\/\" target=\"_blank\" rel=\"nofollow noopener\">www.ascletis.com<\/a>.<\/p>\n<p>Contact\uff1a<\/p>\n<p><span class=\"xn-person\">Peter Vozzo<\/span><br \/>ICR Healthcare<br \/>443-231-0505 (U.S.)<br \/><a href=\"mailto:Peter.vozzo@icrhealthcare.com\" target=\"_blank\" rel=\"nofollow noopener\">Peter.vozzo@icrhealthcare.com<\/a>&nbsp;<\/p>\n<p>Ascletis Pharma Inc. PR and IR teams<br \/>+86-181-0650-9129 (<span class=\"xn-location\">China<\/span>)<br \/><a href=\"mailto:pr@ascletis.com\" target=\"_blank\" rel=\"nofollow noopener\">pr@ascletis.com<\/a> <br \/><a href=\"mailto:ir@ascletis.com\" target=\"_blank\" rel=\"nofollow noopener\">ir@ascletis.com<\/a>&nbsp;<\/p>\n<\/p><\/div>\n<p>Source: Ascletis Pharma Inc.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>&#8211;&nbsp; Utilizing Ascletis&#8217; Peptide Oral Transport ENhancement Technology (POTENT), ASC37 oral tablets achieved average absolute oral bioavailability of 4.2%, approximately 9&#8211;, 30&#8211;, and 60-fold higher than semaglutide, tirzepatide, and retatrutide in the oral SNAC formulation, respectively, in head-to-head non-human primate (NHP) studies. &#8211;&nbsp; ASC37 oral tablets&#8217; drug exposure, as measured by the area under curve [&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-41828","post","type-post","status-publish","format-standard","hentry","category-business-news"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.9 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Ascletis Selects Its First Oral GLP-1R\/GIPR\/GCGR Triple Peptide Agonist, ASC37, for Clinical Development - 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=41828\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Ascletis Selects Its First Oral GLP-1R\/GIPR\/GCGR Triple Peptide Agonist, ASC37, for Clinical Development - My Blog\" \/>\n<meta property=\"og:description\" content=\"&#8211;&nbsp; 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