{"id":39970,"date":"2025-09-18T00:15:00","date_gmt":"2025-09-18T00:15:00","guid":{"rendered":"https:\/\/www.prnasia.com\/story\/archive\/4775783_CN75783_0"},"modified":"2025-09-18T00:15:00","modified_gmt":"2025-09-18T00:15:00","slug":"carsgen-presents-updated-long-term-follow-up-results-for-zevor-cel-at-ims-2025","status":"publish","type":"post","link":"https:\/\/transmediavictoria.net.au\/?p=39970","title":{"rendered":"CARsgen Presents Updated Long-term Follow-up Results for Zevor-cel at IMS 2025"},"content":{"rendered":"<table name=\"logo_release\" border=\"0\" cellspacing=\"10\" cellpadding=\"5\" align=\"right\">\n<tbody>\n<tr>\n<td><img decoding=\"async\" src=\"https:\/\/mma.prnasia.com\/media2\/1722549\/Logo.jpg?p=medium600\" border=\"0\" alt title=\"logo\" hspace=\"0\" vspace=\"0\" width=\"118\"><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span class=\"legendSpanClass\"><span class=\"xn-location\">SHANGHAI<\/span>, Sept. 18, 2025 \/PRNewswire\/ &#8212; CARsgen Therapeutics Holdings Limited (Stock Code: 2171.HK), a company focused on developing innovative CAR T-cell therapies, announces that the updated long-term follow-up results of Phase I clinical trial of zevorcabtagene autoleucel (zevor-cel, R&amp;D code: CT053, an autologous CAR T-cell product targeting BCMA) have been presented as a poster at the 22nd International Myeloma Society (&#8220;IMS&#8221;) Annual Meeting. The poster was titled &#8220;Long term Follow-up of Zevor-cel in Patients with Relapsed\/Refractory Multiple Myeloma&#8221; (Abstract number: PA-029).<\/span><\/p>\n<p>In this study, a total of 14 patients with relapsed or refractory multiple myeloma (R\/R MM) received a single infusion of zevor-cel. As of <span class=\"xn-chron\">February 22, 2025<\/span>, the median follow-up duration was 53.3 months (range:14.8, 63.5).<\/p>\n<p>Regarding safety: There were no reports of \u2265Grade 3 cytokine release syndrome (CRS), immune effector cell-associated neurotoxicity syndrome (ICANS), delayed neurotoxicities, second primary malignancy or other delayed AEs on the study.<\/p>\n<p>Regarding efficacy: The overall response rate was 100% (95% CI: 76.8, 100.0) with 11 (78.6%) patients achieving complete response (CR) or stringent complete response (sCR). All patients who achieved CR or better were minimal residual disease (MRD) negative at 10<sup>\u22125<\/sup> threshold. One patient remained in sCR at 59.3 months in the study. The median progression-free survival (mPFS) and the median duration of response (mDoR) were <b>44.1 months<\/b> and <b>43.2 months<\/b> in CR\/sCR patients, respectively. The median overall survival (OS) was not reached. The proportion of patients surviving at 24, 36, 48 and 60 months after infusion were 100%, 92.3%, 84.6% and <b>76.9%<\/b>, respectively.<\/p>\n<p>At approximately 5 years of follow-up, zevor-cel demonstrates <b>manageable safety profile<\/b> while eliciting <b>deep and durable responses<\/b> in R\/R MM patients.<\/p>\n<p><b>About Zevor-cel<\/b><\/p>\n<p>Zevor-cel is a fully human, autologous BCMA CAR T-cell product for the treatment of Multiple Myeloma (MM). Zevor-cel was approved by the NMPA on <span class=\"xn-chron\">February 23, 2024<\/span> for the treatment of adult patients with R\/R MM who have progressed after at least 3 prior lines of therapy (including a proteasome inhibitor and an immunomodulatory agent). Zevor-cel received Regenerative Medicine Advanced Therapy (RMAT) and Orphan Drug designations from the U.S. FDA in 2019.<\/p>\n<p><b>About CARsgen Therapeutics Holdings Limited<\/b><\/p>\n<p>CARsgen is a biopharmaceutical company focusing on developing innovative CAR T-cell therapies to address the unmet clinical needs including but not limited to hematologic malignancies, solid tumors and autoimmune diseases. CARsgen has established end-to-end capabilities for CAR T-cell research and development covering target discovery, preclinical research, product clinical development, and commercial-scale production. CARsgen has developed novel in-house technologies and a product pipeline with global rights to address challenges faced by existing CAR T-cell therapies. Efforts include improving safety profile, enhancing the efficacy in treating solid tumors, and reducing treatment costs, etc. CARsgen&#8217;s mission is to be a global biopharmaceutical leader that provides innovative and differentiated cell therapies for patients worldwide and makes cancer and other diseases curable.<\/p>\n<p><b>Forward-looking Statements<\/b><\/p>\n<p>All statements in this press release that are not historical fact or that do not relate to present facts or current conditions are forward-looking statements. Such forward-looking statements express the Group&#8217;s current views, projections, beliefs and expectations with respect to future events as of the date of this press release. Such forward-looking statements are based on a number of assumptions and factors beyond the Group&#8217;s control. As a result, they are subject to significant risks and uncertainties, and actual events or results may differ materially from these forward-looking statements and the forward-looking events discussed in this press release might not occur. Such risks and uncertainties include, but are not limited to, those detailed under the heading &#8220;Principal Risks and Uncertainties&#8221; in our most recent annual report and interim report and other announcements and reports made available on our corporate website, <a href=\"https:\/\/www.carsgen.com\" target=\"_blank\" rel=\"nofollow noopener\">https:\/\/www.carsgen.com<\/a>. No representation or warranty is given as to the achievement or reasonableness of, and no reliance should be placed on, any projections, targets, estimates or forecasts contained in this press release.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>SHANGHAI, Sept. 18, 2025 \/PRNewswire\/ &#8212; CARsgen Therapeutics Holdings Limited (Stock Code: 2171.HK), a company focused on developing innovative CAR T-cell therapies, announces that the updated long-term follow-up results of Phase I clinical trial of zevorcabtagene autoleucel (zevor-cel, R&amp;D code: CT053, an autologous CAR T-cell product targeting BCMA) have been presented as a poster at [&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-39970","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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