{"id":37003,"date":"2025-06-03T01:00:00","date_gmt":"2025-06-03T01:00:00","guid":{"rendered":"https:\/\/www.prnasia.com\/story\/archive\/4699711_CN99711_0"},"modified":"2025-06-03T01:00:00","modified_gmt":"2025-06-03T01:00:00","slug":"xellsmart-secures-fda-clearance-for-three-phase-i-inds-of-allogeneic-ipsc-derived-cell-therapies-targeting-major-cns-diseases-parkinsons-diseases-spinal-cord-injury-and-als","status":"publish","type":"post","link":"https:\/\/transmediavictoria.net.au\/?p=37003","title":{"rendered":"XellSmart Secures FDA Clearance for Three Phase I INDs of Allogeneic iPSC-Derived Cell Therapies Targeting Major CNS Diseases: Parkinson&#8217;s Diseases, Spinal Cord Injury and ALS"},"content":{"rendered":"<p><span class=\"legendSpanClass\">SUZHOU, <span class=\"xn-location\">China<\/span><\/span>, <span class=\"legendSpanClass\"><span class=\"xn-chron\">June 3, 2025<\/span><\/span> \/PRNewswire\/ &#8212;<b>&nbsp;XellSmart Biomedical Co., Ltd. (Suzhou\/<span class=\"xn-location\">Shanghai, China<\/span>) is a leading biotechnology company dedicated to the development of innovative iPSC-derived cell therapies. To date, the company has received seven Investigational New Drug (IND) approvals for registered clinical trials from both the National Medical Products Administration (NMPA) of <span class=\"xn-location\">China<\/span> and the U.S. Food and Drug Administration (FDA). All approvals focus on clinical-grade, off-the-shelf and allogeneic iPSC-derived cell therapy candidates targeting central nervous system (CNS) diseases with significant unmet medical needs, including:<\/b><\/p>\n<p><b>Parkinson<\/b><b>&#8216;<\/b><b>s Disease (PD), the world<\/b><b>&#8216;<\/b><b>s second most prevalent neurodegenerative disease affecting over 10 million patients globally (Phase I clinical trials in both <span class=\"xn-location\">China<\/span> and the U.S.); <\/b><\/p>\n<p><b>Spinal Cord Injury (SCI), a major CNS disease impacting more than 10 million patients globally (First-in-Class; Phase I clinical trials in <span class=\"xn-location\">China<\/span> and the U.S.); and <\/b><\/p>\n<p><b>Amyotrophic lateral sclerosis (ALS), a devastating rare neurodegenerative disease (First-in-Class; Phase I\/II clinical trial in <span class=\"xn-location\">China<\/span> and Phase I in the U.S.; designated as an Orphan Drug by the U.S. FDA).<\/b><\/p>\n<p>XellSmart has completed multiple cases of iPSC-derived dopaminergic neural progenitor cell therapy for patients with Parkinson&#8217;s disease, including&#8221;the first case&#8221;in <span class=\"xn-location\">China<\/span>. This clinical study was approved by&nbsp;the National Health Commission (NHC) of <span class=\"xn-location\">China<\/span>. In the clinical study, clinical-grade iPSC-derived dopaminergic neural progenitor cells were transplanted into the putamen of the striatum in patients with moderate to advanced Parkinson&#8217;s disease. With follow-up periods exceeding 12 months, no cell therapy-related adverse events have been observed. Multiple patients showed significant improvements in key efficacy indicators, including&#8221;on\/off&#8221;time duration and MDS-UPDRS scores, as well as notable enhancements in non-motor symptoms.<\/p>\n<p><b>XellSmart is committed to developing clinical-grade, off-the-shelf allogeneic iPSC-derived cell therapies targeting central nervous system (CNS) diseases with no effective treatment options. XellSmart is at the forefront of advancing innovative iPSC-based therapies to address major and intractable CNS disorders:<\/b><br \/><b>In 2023<\/b>, <i><span class=\"xn-location\">China&#8217;s<\/span> first<\/i> iPSC-derived cell therapy (XS228 injection), developed by XellSmart, was granted by FDA as <b>Orphan Drug Designation (ODD)<\/b> for the treatment of amyotrophic lateral sclerosis (ALS).<\/p>\n<p><b>In 2024<\/b>,&nbsp;<i><span class=\"xn-location\">China&#8217;s<\/span> first<\/i> national-level registered clinical study of an iPSC-derived cell therapy for Parkinson&#8217;s disease\u2014also developed by XellSmart\u2014was approved and initiated, including <b>the first case treated in <span class=\"xn-location\">China<\/span><\/b>.<\/p>\n<p><b>In 2024<\/b>, <i>the world&#8217;s first<\/i> national-level registered clinical study of a <b>subtype-specific iPSC-derived neural progenitor cell therapy (XS228 injection)<\/b> for ALS was approved. Multiple patients, including <b>the world&#8217;s first ALS case treated with this approach<\/b>, received therapy with good safety profiles and <b>preliminary data showing slowed disease progression<\/b>.<\/p>\n<p><b>In 2025<\/b>, <i><span class=\"xn-location\">China&#8217;s<\/span> first<\/i>&nbsp;registrational Phase I clinical trial of an<b> off-the-shelf allogeneic iPSC-derived dopaminergic neural progenitor cell therapy (XS411 injection)<\/b> for Parkinson&#8217;s disease was launched, led by the <b>National Neurological Disease Medical Center at Beijing Tiantan Hospital<\/b>.<\/p>\n<p><b>In 2025<\/b>, <i><span class=\"xn-location\">China&#8217;s<\/span> first<\/i> randomized, double-blind, controlled Phase I\/II clinical trial of XS411 injection was initiated to treat <b>early-onset Parkinson&#8217;s disease (EOPD)<\/b>, led by <b>Huashan Hospital of Fudan University<\/b>, a National Neurological Disease Medical Center.<\/p>\n<p><b>In 2025<\/b>, <i>the world&#8217;s first<\/i> registrational Phase I clinical trial of an <b>off-the-shelf, allogeneic iPSC-derived subtype-specific neural progenitor cell therapy<\/b> was launched by <b>The Third Affiliated Hospital of <span class=\"xn-person\">Sun Yat<\/span>-sen University<\/b>, targeting <b>spinal cord injury (SCI) <\/b>\u2014 a major neurological disorder with no effective treatment.<\/p>\n<p><b>In 2025<\/b>, <i>the world&#8217;s first<\/i> Phase I\/II registrational clinical trial of XS228 injection\u2014an <b>off-the-shelf, allogeneic iPSC-derived subtype-specific neural progenitor cell therapy<\/b>\u2014was initiated by <b>Peking University Third Hospital<\/b>, targeting <b>ALS<\/b>, a devastating rare neurodegenerative disease.<\/p>\n<p>XellSmart has established a fully dedicated, internationally competitive &#8220;All-In&#8221; team focusing on development of clinical-grade, allogeneic, off-the-shelf iPSC-derived cell therapies for central nervous system (CNS) diseases that currently lack effective treatment options. XellSmart has built a portfolio of proprietary, globally leading industrial technologies and platforms, fueling sustained in-house innovation centered on its core business. To develop iPSC-derived cell therapy candidates, XellSmart has established and operates an R&amp;D center, a B+ and A-grade GMP manufacturing facility, and a quality control center spanning over 5,000 square meters.<\/p>\n<p>Multiple clinical-grade iPSC-derived cell therapy candidates developed by XellSmart have completed core CMC development, with fully integrated clinical-grade manufacturing processes and quality control systems in place. XellSmart has successfully produced clinical batches of multiple GMP-grade iPSC-derived subtype-specific neural progenitor cell therapies, currently deployed in multiple clinical trials.<\/p>\n<p>XellSmart has secured multiple rounds of financing, collectively led by renowned market-driven venture capital firms including Qiming Venture Partners, Eli Lilly Asia Ventures, Sequoia Capital China (Hongshan), and others.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>SUZHOU, China, June 3, 2025 \/PRNewswire\/ &#8212;&nbsp;XellSmart Biomedical Co., Ltd. (Suzhou\/Shanghai, China) is a leading biotechnology company dedicated to the development of innovative iPSC-derived cell therapies. To date, the company has received seven Investigational New Drug (IND) approvals for registered clinical trials from both the National Medical Products Administration (NMPA) of China and the U.S. [&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-37003","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>XellSmart Secures FDA Clearance for Three Phase I INDs of Allogeneic iPSC-Derived Cell Therapies Targeting Major CNS Diseases: Parkinson&#039;s Diseases, Spinal Cord Injury and ALS - 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=37003\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"XellSmart Secures FDA Clearance for Three Phase I INDs of Allogeneic iPSC-Derived Cell Therapies Targeting Major CNS Diseases: Parkinson&#039;s Diseases, Spinal Cord Injury and ALS - My Blog\" \/>\n<meta property=\"og:description\" content=\"SUZHOU, China, June 3, 2025 \/PRNewswire\/ &#8212;&nbsp;XellSmart Biomedical Co., Ltd. (Suzhou\/Shanghai, China) is a leading biotechnology company dedicated to the development of innovative iPSC-derived cell therapies. 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