{"id":9059,"date":"2022-07-20T13:11:00","date_gmt":"2022-07-20T11:11:00","guid":{"rendered":"https:\/\/czecrin.cz\/project\/kh-kdo_dc1311\/"},"modified":"2026-01-06T09:50:48","modified_gmt":"2026-01-06T08:50:48","slug":"kh-kdo_dc1311","status":"publish","type":"project","link":"https:\/\/czecrin.cz\/en\/project\/kh-kdo_dc1311\/","title":{"rendered":"CT KDO_DC1311"},"content":{"rendered":"\n<h3 class=\"wp-block-heading has-text-align-center\">CLINICAL TRIAL WHO_DC1311<\/h3>\n\n\n\n<hr class=\"wp-block-separator has-text-color has-black-color has-alpha-channel-opacity has-black-background-color has-background\"\/>\n\n\n\n<div style=\"height:30px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<p class=\"has-text-align-center\"><em>Combination anti-tumour therapy with ex vivo manipulated interleukin-12 producing dendritic cells in paediatric, adolescent and young adult patients with progressive, relapsed or primary metastatic high-risk malignancies<\/em><\/p>\n\n\n\n<p class=\"has-text-align-center\">KDO_DC1311 is a phase I\/II clinical trial to evaluate the safety and efficacy of a dendritic cell-based drug in pediatric, adolescent and young adult cancer patients.<\/p>\n\n\n\n<p class=\"has-text-align-center\">The medicinal product was developed and is manufactured by the CZECRIN GMP unit of ACIU MU. The drug is based on the patient&#8217;s own immune cells and a sample of the patient&#8217;s own tumour tissue. In the laboratories, a certain type of the sampled immune cells is allowed to mature and &#8220;learns&#8221; to recognise the sampled tumour cells. After administration of these &#8216;trained&#8217; cells, the patient&#8217;s own anti-tumour defences should be boosted.   <\/p>\n\n\n\n<p class=\"has-text-align-center\">The commissioner of the study is Masaryk University. Patients participating in the study are under the care of the principal investigating physician, Mr. MUDr. Peter M\u00fadr\u00fd, Ph.D. and his colleagues from the Department of Paediatric Oncology, University Hospital Brno. In parallel with the investigational drug, patients undergo all available anti-cancer treatment.    <\/p>\n\n\n\n<h6 class=\"wp-block-heading has-text-align-center\">OVERVIEW OF RECRUITMENT<\/h6>\n\n\n\n<p class=\"has-text-align-center\">Recruitment for the KDO_DC1311 study has been completed. Enrolled patients continue to be seen at the Clinical Paediatric Oncology Unit and their health status and disease progression is monitored. <\/p>\n\n\n\n<figure class=\"wp-block-image aligncenter size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"324\" src=\"https:\/\/czecrin.cz\/wp-content\/uploads\/2022\/07\/Infografika_ZDROJ_ENG-1920x607-1-1024x324.jpg\" alt=\"\" class=\"wp-image-9307\" srcset=\"https:\/\/czecrin.cz\/wp-content\/uploads\/2022\/07\/Infografika_ZDROJ_ENG-1920x607-1-980x310.jpg 980w, https:\/\/czecrin.cz\/wp-content\/uploads\/2022\/07\/Infografika_ZDROJ_ENG-1920x607-1-480x152.jpg 480w\" sizes=\"(min-width: 0px) and (max-width: 480px) 480px, (min-width: 481px) and (max-width: 980px) 980px, (min-width: 981px) 1024px, 100vw\" \/><\/figure>\n\n\n\n<div style=\"height:100px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h2 class=\"wp-block-heading has-text-align-center\">Important links to the project<\/h2>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n\n\n\n<div style=\"height:30px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<figure class=\"wp-block-table\"><table class=\"has-fixed-layout\"><tbody><tr><td class=\"has-text-align-center\" data-align=\"center\"><strong><a href=\"https:\/\/www.clinicaltrialsregister.eu\/ctr-search\/trial\/2014-003388-39\/CZ\" target=\"_blank\" rel=\"noreferrer noopener\">EU Clinical Trials Register<\/a><\/strong><\/td><td class=\"has-text-align-center\" data-align=\"center\"><strong><a href=\"https:\/\/www.frontiersin.org\/articles\/10.3389\/fonc.2019.01169\/full\" target=\"_blank\" rel=\"noreferrer noopener\">Publication Fedorova et al., Front Oncol 2019<\/a><\/strong><\/td><\/tr><tr><td class=\"has-text-align-center\" data-align=\"center\"><strong><a href=\"https:\/\/www.frontiersin.org\/articles\/10.3389\/fonc.2019.01034\/full\" target=\"_blank\" rel=\"noreferrer noopener\">The publication by Hlavackova et. al, Front Oncol 2019 <\/a><\/strong><\/td><td class=\"has-text-align-center\" data-align=\"center\"><strong><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/ijc.35062\" target=\"_blank\" rel=\"noreferrer noopener\">Personalized dendritic cell vaccine in multimodal individualized combination therapy&#8230;, RESEARCH ARTICLE<\/a><\/strong><\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<div style=\"height:100px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h2 class=\"wp-block-heading has-text-align-center\">Project documents<\/h2>\n\n\n\n<hr class=\"wp-block-separator has-text-color has-black-color has-alpha-channel-opacity has-black-background-color has-background\"\/>\n\n\n\n<div style=\"height:30px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<figure class=\"wp-block-table\"><table class=\"has-fixed-layout\"><tbody><tr><td class=\"has-text-align-center\" data-align=\"center\"><strong><a href=\"https:\/\/czecrin.cz\/wp-content\/uploads\/2025\/04\/KDO_DC1311-Approval-SUKL.pdf\">Approval of KH <\/a><a href=\"https:\/\/czecrin.cz\/wp-content\/uploads\/2025\/04\/KDO_DC1311-Approval-SUKL.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">S<\/a><a href=\"https:\/\/czecrin.cz\/wp-content\/uploads\/2025\/04\/KDO_DC1311-Approval-SUKL.pdf\">UKL<\/a><\/strong><\/td><td class=\"has-text-align-center\" data-align=\"center\"><strong><a href=\"https:\/\/czecrin.cz\/wp-content\/uploads\/2025\/04\/KDO_DC1311-Approval-EC.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">Approval of KH EK FN Brno<\/a><\/strong><\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<div style=\"height:20px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<div style=\"height:100px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h5 class=\"wp-block-heading has-text-align-center\">Contact<\/h5>\n\n\n\n<p class=\"has-text-align-center has-medium-font-size\"><a href=\"mailto:ctc.czecrin@med.muni.cz\">ctc.czecrin@med.muni.cz<\/a><\/p>\n\n\n\n<div style=\"height:30px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<ul class=\"wp-block-social-links aligncenter is-layout-flex wp-block-social-links-is-layout-flex\"><li class=\"wp-social-link wp-social-link-x  wp-block-social-link\"><a href=\"https:\/\/twitter.com\/intent\/tweet?hashtags=remed%2Cczecrin%2Cclinicaltrials&#038;original_referer=https%3A%2F%2Fczecrin.cz%2F&#038;ref_src=twsrc%5Etfw%7Ctwcamp%5Ebuttonembed%7Ctwterm%5Eshare%7Ctwgr%5E&#038;related=%40czecrin&#038;text=KH%20KDO_DC1311%20-%20Czecrin&#038;url=https%3A%2F%2Fczecrin.cz%2Fprojekty%2Fkh-kdo-dc-1311%2F\" class=\"wp-block-social-link-anchor\"><svg width=\"24\" height=\"24\" viewBox=\"0 0 24 24\" version=\"1.1\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" aria-hidden=\"true\" focusable=\"false\"><path d=\"M13.982 10.622 20.54 3h-1.554l-5.693 6.618L8.745 3H3.5l6.876 10.007L3.5 21h1.554l6.012-6.989L15.868 21h5.245l-7.131-10.378Zm-2.128 2.474-.697-.997-5.543-7.93H8l4.474 6.4.697.996 5.815 8.318h-2.387l-4.745-6.787Z\" \/><\/svg><span class=\"wp-block-social-link-label screen-reader-text\">X<\/span><\/a><\/li><\/ul>\n","protected":false},"excerpt":{"rendered":"<p>CLINICAL TRIAL WHO_DC1311 Combination anti-tumour therapy with ex vivo manipulated interleukin-12 producing dendritic cells in paediatric, adolescent and young adult patients with progressive, relapsed or primary metastatic high-risk malignancies KDO_DC1311 is a phase I\/II clinical trial to evaluate the safety and efficacy of a dendritic cell-based drug in pediatric, adolescent and young adult cancer patients. [&hellip;]<\/p>\n","protected":false},"author":5,"featured_media":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"_et_pb_use_builder":"","_et_pb_old_content":"","_et_gb_content_width":"","inline_featured_image":false,"footnotes":""},"project_category":[147,146],"project_tag":[157,158,148,153,155,150],"class_list":["post-9059","project","type-project","status-publish","hentry","project_category-national-research-projects","project_category-ongoing-clinical-trials","project_tag-atmp","project_tag-immunotherapy","project_tag-oncology","project_tag-pediatrics","project_tag-phase-i","project_tag-phase-ii"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.2 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>CT KDO_DC1311 &#8226; CZECRIN - \u010cesk\u00e1 n\u00e1rodn\u00ed s\u00ed\u0165 pro podporu klinick\u00e9ho v\u00fdzkumu<\/title>\n<meta name=\"description\" content=\"Effect of dexamethasone in patients with ARDS and COVID-19 - a prospective, multicentre, open-label, randomised controlled trial with parallel groups.COVID-19 is still a major challenge for medical research, with new drugs or possible optimisation of existing drugs being investigated. One possibility to use an existing drug is treatment with the corticosteroid dexamethasone. The REMED clinical trial is designed to test the hypothesis that administration of 20 mg dexamethasone daily is more effective compared to a daily dose of 6 mg dexamethasone in adult patients with moderate or severe ARDS related to COVID-19. The initiator of this multicentre study is the University Hospital Brno - Department of Anaesthesiology, Resuscitation and Intensive Medicine, which in collaboration with VI CZECRIN is conducting the study in 10 centres in the Czech Republic in 300 patients.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/czecrin.cz\/en\/project\/kh-kdo_dc1311\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"CT KDO_DC1311 &#8226; CZECRIN - \u010cesk\u00e1 n\u00e1rodn\u00ed s\u00ed\u0165 pro podporu klinick\u00e9ho v\u00fdzkumu\" \/>\n<meta property=\"og:description\" content=\"Effect of dexamethasone in patients with ARDS and COVID-19 - a prospective, multicentre, open-label, randomised controlled trial with parallel groups.COVID-19 is still a major challenge for medical research, with new drugs or possible optimisation of existing drugs being investigated. 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