{"id":26730,"date":"2024-05-24T12:00:00","date_gmt":"2024-05-24T12:00:00","guid":{"rendered":"https:\/\/www.prnasia.com\/story\/archive\/4422994_CN22994_0"},"modified":"2024-05-24T12:00:00","modified_gmt":"2024-05-24T12:00:00","slug":"juncell-therapeutics-announces-clinical-data-of-gc203-til-therapy-in-ovarian-cancer-at-asco-2024","status":"publish","type":"post","link":"https:\/\/transmediavictoria.net.au\/?p=26730","title":{"rendered":"Juncell Therapeutics Announces Clinical Data of GC203 TIL therapy in Ovarian Cancer at ASCO 2024"},"content":{"rendered":"\n<p><span class=\"legendSpanClass\"><span class=\"xn-location\">SHANGHAI<\/span><\/span>, <span class=\"legendSpanClass\"><span class=\"xn-chron\">May 24, 2024<\/span><\/span> \/PRNewswire\/ &#8212; Shanghai Juncell Therapeutics Co., Ltd. (Juncell Therapeutics), a clinical-stage biotech developing innovative Tumor-Infiltrating Lymphocyte (TIL) therapies for cancers, announced latest clinical research results on GC203 (a novel non-viral vector gene-modified TIL therapy engineered with membrane-bound IL-7). These data will be presented at the American Society of Clinical Oncology (ASCO) Annual Meeting taking place on <span class=\"xn-chron\">May 31 &#8211; June 4, 2024<\/span>.<\/p>\n<p>Researchers tested GC203 on patients diagnosed with recurrent ovarian cancer, without the combination of IL-2 administration or aggressive lymphodepletion. The objective of the study was to determine the safety and efficacy of this treatment. A total of 20 patients were enrolled between 09\/2021 and 01\/2024 in the open-label single-center trial, in which 18 patients were evaluable. The evaluable patients were with an ECOG PS of 1 (55.6%) or 2 (44.4%) and received a median of 5 previous systemic therapies (range: 2-11). 9 (50%) patients had 3 or more tumor lesions. The median target lesion size was 57 (range: 13-146) mm.<\/p>\n<p>GC203 showed promising results in patients with recurrent or metastatic ovarian cancer. The safety profile was improved significantly compared with conventional TIL therapies, thanks to a low-intensity pretreatment and the elimination of IL-2 combination. Most of the Adverse Events (AEs) were grade 1 or grade 2 and could be alleviated or cured by symptomatic treatment. No grade 5 event occurred. By the cutoff date of 01\/2024, the investigator-assessed Objective Response Rate (ORR) was 33.3% (95% CI: 16.3 &#8211; 56.3), including 11.1% Complete Response (CR). The Disease Control Rate (DCR) was 83.3% (95% CI, 60.8 &#8211; 94.2). And the 12-month Overall Survival (OS) rate was 68.8% (95% CI: 49.3 &#8211; 95.9). The median OS was not mature as data cut-off.<\/p>\n<p><b>Presentation Details<\/b><\/p>\n<p><b>Abstract Number:<\/b> 5552<\/p>\n<p><b>Abstract Title:<\/b> A phase I single-arm, open-label trial of engineering tumor-infiltrating lymphocytes with membrane-bound lL-7 for recurrent ovarian cancer.<\/p>\n<p><b>Session Type and Title:<\/b> Poster Session &#8211; Gynecologic Oncology<\/p>\n<p><b>Poster Presentation Time:<\/b> <span class=\"xn-chron\">9:00 AM &#8211; 12:00 PM CDT<\/span>, <span class=\"xn-chron\">June 3, 2024<\/span><\/p>\n<p><b>Presenter:<\/b> Dr. <span class=\"xn-person\">Jing Guo<\/span>, Shanghai Tenth People&#8217;s Hospital<\/p>\n<p>The abstract is available on the ASCO website.<\/p>\n<p><b>About Ovarian Cancer<\/b><\/p>\n<p>Ovarian cancer has the highest mortality rate among gynecologic cancers. 70% of patients are diagnosed at an advanced stage. 70% of patients with advanced ovarian cancer have a survival time of less than five years. More than 200,000 people worldwide die from ovarian cancer each year, indicating a significant unmet clinical need. The primary treatment for advanced ovarian cancer is platinum-based chemotherapy. Ovarian cancer is insensitive to immunotherapy, with an ORR of less than 10%. Effective treatment options are limited.<\/p>\n<p><b>About GC203<\/b><\/p>\n<p>GC203 is a novel non-viral vector gene-modified TIL therapy developed leveraging Juncell Therapeutics&#8217; proprietary DeepTIL<sup>&reg;<\/sup> cell expansion platform and NovaGMP<sup>&reg;<\/sup> gene modification platform. DeepTIL<sup>&reg;<\/sup> enables TILs to be potent enough that no IL-2 combination will be required after infusion, and the intensity of pretreatment could be lower. NovaGMP<sup>&reg;<\/sup> modifies T cells with a high efficiency comparable with the Lentiviral vector in an economic way. GC203 is engineered with self-associating membrane-bound interleukin-7, which can maintain the stemness of memory T cells, activate internal immune cells and avoid systemic toxicities.<\/p>\n<p><b>About Juncell Therapeutics<\/b><\/p>\n<p>Juncell Therapeutics is a biotech dedicated to developing high-quality, accessible TIL cell therapies for the treatment of solid tumors. Juncell Therapeutics has established its proprietary DeepTIL<sup>&reg;<\/sup> cell expansion and NovaGMP<sup>&reg;<\/sup> gene modification technology platforms, which are designed to address the key challenges of conventional TIL therapies, making TILs &quot;robust, competent, affordable, and accessible.&quot; Two clinical-stage TIL therapies have demonstrated promising safety and efficacy in the treatment of nine types of heavily pretreated advanced solid tumors, including lung cancer, triple-negative breast cancer, pancreatic cancer, high-grade glioma, ovarian cancer, endometrial cancer, cervical cancer, bile duct cancer and melanoma. 7 of these late-stage tumor patients have achieved CR, and the longest tumor-free survival time is approaching 3 years.<\/p>\n<p>For more information, please visit:<br \/><a href=\"https:\/\/www.juncell.com\/en\" target=\"_blank\" rel=\"nofollow noopener\">https:\/\/www.juncell.com\/en<\/a><br \/><a href=\"https:\/\/www.linkedin.com\/company\/juncell-therapeutics\" target=\"_blank\" rel=\"nofollow noopener\">https:\/\/www.linkedin.com\/company\/juncell-therapeutics<\/a><\/p>\n<p>Juncell Contact:<br \/><a href=\"mailto:contact@juncell.com\" target=\"_blank\" rel=\"nofollow noopener\">contact@juncell.com<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>SHANGHAI, May 24, 2024 \/PRNewswire\/ &#8212; Shanghai Juncell Therapeutics Co., Ltd. (Juncell Therapeutics), a clinical-stage biotech developing innovative Tumor-Infiltrating Lymphocyte (TIL) therapies for cancers, announced latest clinical research results on GC203 (a novel non-viral vector gene-modified TIL therapy engineered with membrane-bound IL-7). These data will be presented at the American Society of Clinical Oncology (ASCO) [&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-26730","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>Juncell Therapeutics Announces Clinical Data of GC203 TIL therapy in Ovarian Cancer at ASCO 2024 - 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=26730\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Juncell Therapeutics Announces Clinical Data of GC203 TIL therapy in Ovarian Cancer at ASCO 2024 - My Blog\" \/>\n<meta property=\"og:description\" content=\"SHANGHAI, May 24, 2024 \/PRNewswire\/ &#8212; Shanghai Juncell Therapeutics Co., Ltd. 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