{"id":1616,"date":"2026-04-23T19:04:16","date_gmt":"2026-04-23T19:04:16","guid":{"rendered":"https:\/\/admarebio.com\/news-events\/news-insights\/"},"modified":"2026-06-26T13:07:30","modified_gmt":"2026-06-26T13:07:30","slug":"epitopea-announces-approval-of-ovact-clinical-trial-application-for-cryptivax-1001-in-advanced-high-grade-serous-ovarian-cancer","status":"publish","type":"post","link":"https:\/\/admarebio.com\/news-events\/news-insights\/epitopea-announces-approval-of-ovact-clinical-trial-application-for-cryptivax-1001-in-advanced-high-grade-serous-ovarian-cancer\/","title":{"rendered":"Epitopea Announces Approval of OVACT Clinical Trial Application for CryptiVax-1001 in Advanced High-Grade Serous Ovarian Cancer"},"content":{"rendered":"\n<p><strong>CAMBRIDGE, UK and MONTREAL, CANADA,&nbsp;23&nbsp;April&nbsp;2026<\/strong>&nbsp;\u2013&nbsp;Epitopea,&nbsp;a transatlantic biotech&nbsp;developing&nbsp;off-the-shelf, durable,&nbsp;RNA-based&nbsp;cancer&nbsp;immunotherapies, today announced&nbsp;that it has&nbsp;received approval from the&nbsp;UK\u2019s&nbsp;Medicines and Healthcare products Regulatory Agency (MHRA)&nbsp;and the Regional Ethics Committee (REC)&nbsp;for its&nbsp;clinical trial application (CTA)&nbsp;for&nbsp;its&nbsp;first-in-human clinical trial&nbsp;(OVACT) of its&nbsp;lead program,&nbsp;CryptiVax\u2122-1001,&nbsp;targeting&nbsp;advanced&nbsp;high-grade serous ovarian cancer.&nbsp;<\/p>\n\n\n\n<p>Epitopea&nbsp;also announces&nbsp;the appointment of Professor Susana Banerjee&nbsp;(MBBS MA PhD FRCP),&nbsp;a Consultant Medical Oncologist and Research Lead for the&nbsp;Gynaecology&nbsp;Unit at\u202f<a href=\"https:\/\/www.royalmarsden.nhs.uk\/\" rel=\"noreferrer noopener\" target=\"_blank\">The Royal Marsden<\/a>&nbsp;NHS Foundation Trust&nbsp;and Professor in Women\u2019s Cancers at the Institute of Cancer Research,&nbsp;as Chief Investigator&nbsp;of&nbsp;the OVACT trial.<\/p>\n\n\n\n<p>Dr. Klaus Edvardsen, MD, Chief Medical Officer of&nbsp;Epitopea, commented, \u201cWe are&nbsp;excited by the achievement of this&nbsp;significant regulatory milestone,&nbsp;which is a credit to our dedicated clinical and wider&nbsp;Epitopea&nbsp;team. We&nbsp;also&nbsp;welcome&nbsp;Professor Banerjee&nbsp;to her role as&nbsp;Chief Investigator of&nbsp;our first&nbsp;clinical trial. Her world-class&nbsp;expertise&nbsp;in ovarian cancer and&nbsp;leadership in global clinical development&nbsp;will&nbsp;bring invaluable insights&nbsp;as we transition to a clinical-stage company.\u201d<\/p>\n\n\n\n<p>OVACT is a Phase 1\/1b dose escalation and expansion trial designed to evaluate the safety, tolerability, immunogenicity, and early clinical activity of&nbsp;CryptiVax\u2122-1001&nbsp;in HRP+\/BRCA-wildtype&nbsp;high-grade serous ovarian cancer&nbsp;patients.&nbsp;<\/p>\n\n\n\n<p>High-Grade Serous Ovarian Cancer(HGSOC)&nbsp;remains&nbsp;one of the most difficult-to-treat solid&nbsp;tumors, with&nbsp;most&nbsp;patients (~80%) presenting with advanced or metastatic disease. While most&nbsp;women&nbsp;respond to first-line platinum chemotherapy,&nbsp;nearly all&nbsp;ultimately relapse and progress to platinum-resistant disease. Existing maintenance options&nbsp;leave&nbsp;a major therapeutic gap among HRP+\/BRCA-wildtype patients, who&nbsp;represent&nbsp;roughly half&nbsp;of the&nbsp;ovarian cancer&nbsp;population.&nbsp;<\/p>\n\n\n\n<p>Professor Banerjee added: \u201cThere is a substantial unmet need&nbsp;in&nbsp;homologous recombination proficient (HRP)&nbsp;ovarian cancer, where available maintenance therapies deliver limited durable&nbsp;benefit.&nbsp;Epitopea\u2019s&nbsp;CryptiVax\u2122-1001 vaccine, which targets a novel repertoire of&nbsp;tumor-specific antigens, has the potential to meaningfully extend remission for patients with few effective&nbsp;treatment&nbsp;options.\u201d&nbsp;<\/p>\n\n\n\n<p>Epitopea\u2019s&nbsp;pipeline is enabled by CryptoMap<sup>TM<\/sup>, a&nbsp;proprietary&nbsp;discovery engine that&nbsp;identifies&nbsp;tumor-presented antigens arising from the dark genome,&nbsp;a previously inaccessible source of novel,&nbsp;tumor-specific targets. These antigens, known as&nbsp;Cryptigens<sup>TM<\/sup>,&nbsp;demonstrate&nbsp;high inter-patient sharing, enabling&nbsp;development&nbsp;of true off-the-shelf mRNA&nbsp;immunotherapies.&nbsp;<\/p>\n\n\n\n<p><strong>About&nbsp;Epitopea<\/strong>&nbsp;<br>Epitopea&nbsp;is a transatlantic cancer&nbsp;immunotherapeutics&nbsp;company developing accessible, off-the-shelf RNA-based immunotherapies for hard-to-treat solid&nbsp;tumors.&nbsp;Epitopea\u2019s&nbsp;pipeline is built on&nbsp;Cryptigen\u2122 TSAs, a new class of&nbsp;tumor-specific antigens&nbsp;identified&nbsp;by&nbsp;CryptoMap\u2122, the company\u2019s proprietary immunopeptidomics&nbsp;and genomics platform that uncovers aberrantly expressed antigens arising from previously uncharacterised regions of the genome.&nbsp;<\/p>\n\n\n\n<p>The company\u2019s lead candidate,&nbsp;CryptiVax\u2122-1001, is an off-the-shelf mRNA therapeutic vaccine in development for high-grade serous ovarian cancer. It is designed to drive targeted immune responses using a set of&nbsp;tumor-specific antigens chosen for broad patient coverage. Many patients with advanced cancers, including high-grade serous ovarian cancer, have limited durable treatment options and few effective therapies beyond biomarker-selected populations.&nbsp;Epitopea&nbsp;aims to address this unmet need with&nbsp;broadly applicable,&nbsp;tumor-selective immunotherapies.<br>&nbsp;<br>Backed by leading life-science investors,&nbsp;Epitopea&nbsp;operates from Cambridge, UK, and Montreal, Canada. For more information, visit\u202f<a href=\"http:\/\/www.epitopea.com\/\" rel=\"noreferrer noopener\" target=\"_blank\"><strong>www.epitopea.com<\/strong><\/a>\u202fand follow the company on\u202f<a href=\"https:\/\/www.linkedin.com\/company\/epitopea\/?viewAsMember=true\" rel=\"noreferrer noopener\" target=\"_blank\"><strong>LinkedIn<\/strong><\/a>.&nbsp;<\/p>\n\n\n\n<p><strong>For further information<\/strong>&nbsp;<br><strong>Epitopea\u202f<\/strong>&nbsp;<br>Dr. Alan C. Rigby \u2013 CEO\u202f&nbsp;<br><a href=\"mailto:Alan.Rigby@epitopea.com\" rel=\"noreferrer noopener\" target=\"_blank\">Alan.Rigby@epitopea.com<\/a>&nbsp;<\/p>\n\n\n\n<p><strong>Scius&nbsp;Communications\u202f(for&nbsp;Epitopea)\u202f<\/strong>&nbsp;<br>Katja Stout\u202f&nbsp;<br>+44 7789 435990\u202f&nbsp;<br><a href=\"mailto:katja@sciuscommunications.com\" rel=\"noreferrer noopener\" target=\"_blank\">katja@sciuscommunications.com<\/a>&nbsp;<\/p>\n\n\n\n<p>Daniel Gooch\u202f&nbsp;<br>+44 7747 875479\u202f&nbsp;<br><a href=\"mailto:daniel@sciuscommunications.com\" rel=\"noreferrer noopener\" target=\"_blank\">daniel@sciuscommunications.com<\/a>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>CAMBRIDGE, UK and MONTREAL, CANADA,&nbsp;23&nbsp;April&nbsp;2026&nbsp;\u2013&nbsp;Epitopea,&nbsp;a transatlantic biotech&nbsp;developing&nbsp;off-the-shelf, durable,&nbsp;RNA-based&nbsp;cancer&nbsp;immunotherapies, today announced&nbsp;that it has&nbsp;received approval from the&nbsp;UK\u2019s&nbsp;Medicines and Healthcare products Regulatory Agency (MHRA)&nbsp;and the Regional Ethics Committee (REC)&nbsp;for its&nbsp;clinical trial application (CTA)&nbsp;for&nbsp;its&nbsp;first-in-human [&hellip;]<\/p>\n","protected":false},"author":4,"featured_media":1617,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[29],"tags":[],"company":[78],"class_list":["post-1616","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-portfolio-companies"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.9 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Epitopea Announces Approval of OVACT Clinical Trial Application for CryptiVax-1001 in Advanced High-Grade Serous Ovarian Cancer | adMare<\/title>\n<meta name=\"robots\" content=\"noindex, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" 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