{"id":49685,"date":"2022-10-17T14:02:19","date_gmt":"2022-10-17T12:02:19","guid":{"rendered":"https:\/\/pharma-trend.com\/en\/eureka-therapeutics-receives-orphan-drug-designations-for-treatment-of-hepatoblastoma-with-et140203-artemis-t-cells\/"},"modified":"2022-10-17T14:02:19","modified_gmt":"2022-10-17T12:02:19","slug":"eureka-therapeutics-receives-orphan-drug-designations-for-treatment-of-hepatoblastoma-with-et140203-artemis-t-cells","status":"publish","type":"post","link":"https:\/\/pharma-trend.com\/en\/eureka-therapeutics-receives-orphan-drug-designations-for-treatment-of-hepatoblastoma-with-et140203-artemis-t-cells\/","title":{"rendered":"Eureka Therapeutics Receives Orphan Drug Designations for Treatment of Hepatoblastoma with ET140203 ARTEMIS\u00ae T cells"},"content":{"rendered":"<div>\n<p>EMERYVILLE, Calif.&#8211;(BUSINESS WIRE)&#8211;Eureka Therapeutics, Inc., a clinical-stage biotechnology company developing novel T-cell therapies to treat solid tumors, today announced that the U.S. Food and Drug Administration (FDA) has granted <a target=\"_blank\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=https%3A%2F%2Fwww.fda.gov%2Findustry%2Fdeveloping-products-rare-diseases-conditions%2Fdesignating-orphan-product-drugs-and-biological-products&amp;esheet=52943834&amp;newsitemid=20221017005035&amp;lan=en-US&amp;anchor=Orphan+Drug+Designation+%28ODD%29&amp;index=1&amp;md5=2de22f5cef4ddd397d52c886b22b57b5\" rel=\"nofollow noopener\" shape=\"rect\">Orphan Drug Designation (ODD)<\/a> to ET140203 for the treatment of hepatoblastoma (HB), a rare childhood tumor in the liver that typically occurs in children under the age of 5.\n<\/p>\n<p><a href=\"https:\/\/mms.businesswire.com\/media\/20221017005035\/en\/776975\/5\/Eureka%C2%AE_logo_final_rgb_600.jpg\"><img decoding=\"async\" src=\"https:\/\/mms.businesswire.com\/media\/20221017005035\/en\/776975\/21\/Eureka%C2%AE_logo_final_rgb_600.jpg\"><\/a><\/p>\n<p>\n\u201cWe are pleased to receive ODD for ET140203 following the FDA\u2019s earlier grant of <a target=\"_blank\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=https%3A%2F%2Fwww.fda.gov%2Fpatients%2Ffast-track-breakthrough-therapy-accelerated-approval-priority-review%2Ffast-track&amp;esheet=52943834&amp;newsitemid=20221017005035&amp;lan=en-US&amp;anchor=Fast+Track+Designation+%28FTD%29&amp;index=2&amp;md5=28d204f987a7a2c4b706425476d6a5a9\" rel=\"nofollow noopener\" shape=\"rect\">Fast Track Designation (FTD)<\/a> and <a target=\"_blank\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=https%3A%2F%2Fwww.fda.gov%2Findustry%2Fdeveloping-products-rare-diseases-conditions%2Frare-pediatric-disease-rpd-designation-and-voucher-programs&amp;esheet=52943834&amp;newsitemid=20221017005035&amp;lan=en-US&amp;anchor=Rare+Pediatric+Disease+Designation+%28RPDD%29&amp;index=3&amp;md5=0ba201c6529a053961931059c7234c1d\" rel=\"nofollow noopener\" shape=\"rect\">Rare Pediatric Disease Designation (RPDD)<\/a> designations to ET140203 for the treatment of HB,\u201d said Dr. Cheng Liu, President and CEO of Eureka Therapeutics. \u201cThese designations highlight the significant unmet medical need for better pediatric liver cancer treatment options.\u201d\n<\/p>\n<p>\nEureka is currently recruiting patients in three Phase I\/II clinical trials to investigate the safety and potential efficacy of ARTEMIS<sup>\u00ae<\/sup> T cells that have been engineered to target specific liver cancer antigens. The <a target=\"_blank\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=https%3A%2F%2Fclinicaltrials.gov%2Fct2%2Fshow%2FNCT04502082&amp;esheet=52943834&amp;newsitemid=20221017005035&amp;lan=en-US&amp;anchor=ARYA-1&amp;index=4&amp;md5=a5a7e10cdb9792685e9bb63e98d5564d\" rel=\"nofollow noopener\" shape=\"rect\">ARYA-1<\/a> (adult) and <a target=\"_blank\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=https%3A%2F%2Fclinicaltrials.gov%2Fct2%2Fshow%2FNCT04634357&amp;esheet=52943834&amp;newsitemid=20221017005035&amp;lan=en-US&amp;anchor=ARYA-2&amp;index=5&amp;md5=56c2a2d842c83ed48e81bb3af3621f70\" rel=\"nofollow noopener\" shape=\"rect\">ARYA-2<\/a> (pediatric) studies use ET140203 ARTEMIS T cells directed with a TCR mimic antibody to target an alpha fetoprotein (AFP)-peptide\/HLA-A2 complex found on liver cancer cells. The <a target=\"_blank\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=https%3A%2F%2Fclinicaltrials.gov%2Fct2%2Fshow%2FNCT04864054%3Fterm%3DARYA-3%26draw%3D2%26rank%3D1&amp;esheet=52943834&amp;newsitemid=20221017005035&amp;lan=en-US&amp;anchor=ARYA-3&amp;index=6&amp;md5=f84e9c7691b954795ee69e5760eac3ec\" rel=\"nofollow noopener\" shape=\"rect\">ARYA-3<\/a> study uses ECT204 T cells to target the Glypican 3 (GPC3) protein expressed on the surface of liver cancer cells.\n<\/p>\n<p>\nFDA Orphan Drug Designation is granted to investigational therapies addressing rare medical diseases or conditions that affect fewer than 200,000 people in the United States. Orphan drug status provides benefits to drug developers, including assistance in the drug development process, tax credits for clinical costs, exemptions from certain FDA fees and seven years of post-approval marketing exclusivity.\n<\/p>\n<p>\nPatients, caregivers and health care professionals interested in Eureka\u2019s clinical trials and technology can find more information by visiting <a target=\"_blank\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=http%3A%2F%2Fwww.eurekaconnectme.com%2F&amp;esheet=52943834&amp;newsitemid=20221017005035&amp;lan=en-US&amp;anchor=eurekaconnectme.com&amp;index=7&amp;md5=75a88185efcfffb7bdbb22648438024a\" rel=\"nofollow noopener\" shape=\"rect\">eurekaconnectme.com<\/a>.\n<\/p>\n<p>\n<b>About ARYA-2 Trial and ET140203<\/b>\n<\/p>\n<p>\nThe ARYA-2 study is an open-label, dose escalation, multi-center, Phase I\/II clinical trial designed to assess the safety\/tolerability and preliminary efficacy of ET140203 T-cells in pediatric subjects who are AFP-positive\/HLA-A2-positive and have relapsed\/refractory hepatoblastoma (HB), hepatocellular malignant neoplasm, not otherwise specified (HCN-NOS), or hepatocellular carcinoma (HCC). Additional information about Eureka\u2019s Phase I\/II study may be found at <a target=\"_blank\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=https%3A%2F%2Fclinicaltrials.gov%2Fct2%2Fshow%2FNCT04634357&amp;esheet=52943834&amp;newsitemid=20221017005035&amp;lan=en-US&amp;anchor=ClinicalTrials.gov&amp;index=8&amp;md5=6d57906307d70115d64d53b568e1ed37\" rel=\"nofollow noopener\" shape=\"rect\">ClinicalTrials.gov<\/a>, using Identifier NCT: NCT04634357.\n<\/p>\n<p>\nET140203 is an investigational therapy during which a patient\u2019s T cells are collected, engineered to express Eureka\u2019s proprietary ARTEMIS<sup>\u00ae<\/sup> cell receptor and infused back into the patient. Engineered ET140203 T cells express a TCR-mimic antibody to target an alpha fetoprotein (AFP)-peptide\/HLA-A2 complex on liver cancer cells. In addition, ET140203 ARTEMIS<sup>\u00ae<\/sup> T cells also incorporate Eureka\u2019s proprietary tumor infiltration technology demonstrating enhanced ability to infiltrate solid tumors in animal models, potentially leading to improved efficacy in patients.\n<\/p>\n<p>\n<b>About Eureka Therapeutics, Inc.<\/b>\n<\/p>\n<p>\nEureka Therapeutics, Inc. is a privately held clinical-stage biotechnology company focused on developing novel T cell therapies to treat cancers. Its core technology centers around its proprietary <a target=\"_blank\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41421-018-0066-6&amp;esheet=52943834&amp;newsitemid=20221017005035&amp;lan=en-US&amp;anchor=ARTEMIS%26%23174%3B+cell+receptor&amp;index=9&amp;md5=5391e69ef1246f7ddfad3b56cfb70987\" rel=\"nofollow noopener\" shape=\"rect\">ARTEMIS<sup>\u00ae<\/sup> cell receptor<\/a> platform and E-ALPHA<sup>\u00ae<\/sup> antibody discovery platform for the discovery and development of potentially safer and more effective T cell therapies for the treatment of solid tumors and hematologic malignancies. The company currently has two clinical programs, ET140203 (ARYA1 and ARYA2) and ECT204 (ARYA3), in Phase I\/II US trials in patients with advanced liver cancer.\n<\/p>\n<p>\nEureka Therapeutics, Inc. is headquartered in the San Francisco Bay Area. For more information on Eureka, please visit <a target=\"_blank\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=https%3A%2F%2Fwww.eurekatherapeutics.com%2F&amp;esheet=52943834&amp;newsitemid=20221017005035&amp;lan=en-US&amp;anchor=www.eurekatherapeutics.com&amp;index=10&amp;md5=078999f7f8f04c199acd4971e3234d10\" rel=\"nofollow noopener\" shape=\"rect\">www.eurekatherapeutics.com<\/a>.\n<\/p>\n<p> <b>Contacts<\/b> <\/p>\n<p>\nEureka Therapeutics Inc.<br \/>\n<br \/>Natalie Liu<br \/>\n<br \/>Investor Relations<br \/>\n<br \/>925-605-8033<br \/>\n<br \/><a target=\"_blank\" href=\"&#x6d;&#97;&#x69;&#x6c;&#116;&#x6f;&#x3a;&#73;&#x52;&#x40;&#101;&#x75;&#x72;e&#x6b;&#x61;i&#x6e;&#99;&#46;&#x63;&#111;m\" rel=\"nofollow noopener\" shape=\"rect\">IR&#64;eurekainc&#46;&#99;&#111;&#109;<\/a>\n<\/p>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>EMERYVILLE, Calif.&#8211;(BUSINESS WIRE)&#8211;Eureka Therapeutics, Inc., a clinical-stage biotechnology company developing novel T-cell therapies to treat solid tumors, today announced that the U.S. Food and Drug Administration (FDA) has granted Orphan Drug Designation (ODD) to ET140203 for the treatment of hepatoblastoma (HB), a rare childhood tumor in the liver that typically occurs in children under the &#8230; <span class=\"more\"><a class=\"more-link\" href=\"https:\/\/pharma-trend.com\/en\/eureka-therapeutics-receives-orphan-drug-designations-for-treatment-of-hepatoblastoma-with-et140203-artemis-t-cells\/\">[Read more&#8230;]<\/a><\/span><\/p>\n","protected":false},"author":4,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[13],"tags":[],"class_list":{"0":"entry","1":"post","2":"publish","3":"author-business","4":"post-49685","6":"format-standard","7":"category-industry"},"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.5 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Eureka Therapeutics Receives Orphan Drug Designations for Treatment of Hepatoblastoma with ET140203 ARTEMIS\u00ae T cells - Pharma Trend<\/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:\/\/pharma-trend.com\/en\/eureka-therapeutics-receives-orphan-drug-designations-for-treatment-of-hepatoblastoma-with-et140203-artemis-t-cells\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Eureka Therapeutics Receives Orphan Drug Designations for Treatment of Hepatoblastoma with ET140203 ARTEMIS\u00ae T cells - Pharma Trend\" \/>\n<meta property=\"og:description\" content=\"EMERYVILLE, Calif.&#8211;(BUSINESS WIRE)&#8211;Eureka Therapeutics, Inc., a clinical-stage biotechnology company developing novel T-cell therapies to treat solid tumors, today announced that the U.S. Food and Drug Administration (FDA) has granted Orphan Drug Designation (ODD) to ET140203 for the treatment of hepatoblastoma (HB), a rare childhood tumor in the liver that typically occurs in children under the ... 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