{"id":9062,"date":"2022-06-23T12:41:00","date_gmt":"2022-06-23T10:41:00","guid":{"rendered":"https:\/\/czecrin.cz\/project\/kh-half\/"},"modified":"2026-01-06T09:56:23","modified_gmt":"2026-01-06T08:56:23","slug":"kh-half","status":"publish","type":"project","link":"https:\/\/czecrin.cz\/en\/project\/kh-half\/","title":{"rendered":"CT HALF"},"content":{"rendered":"\n<h3 class=\"wp-block-heading has-text-align-center\">CLINICAL TRIAL HALF<\/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>Prospective phase II clinical trial evaluating the efficacy and safety of tyrosine kinase inhibitor discontinuation after prior two-step dose reduction in patients with chronic myeloid leukemia in deep molecular remission<\/em><\/p>\n\n\n\n<p class=\"has-text-align-center\">The HALF clinical trial is designed as a prospective, multicentre, non-randomised, open-label phase II study to assess the efficacy and safety of tyrosine kinase inhibitor withdrawal after prior two-step dose reduction in patients with chronic myeloid leukaemia in deep remission. The HALF clinical trial could contribute to the formulation of a new disease management strategy for patients achieving sustained remission with the potential for wider benefits not only for the patients themselves but also for the healthcare system. <\/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\">The planned number of subjects for the HALF study was 150 patients. This number was reached in January 2022. Recruitment was completed as of June 30, 2023 with a total of 221 patients enrolled. The infographic below shows the involvement of the collaborating sites in terms of number of subjects enrolled.   <\/p>\n\n\n\n<figure class=\"wp-block-image aligncenter size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"415\" src=\"https:\/\/czecrin.cz\/wp-content\/uploads\/2022\/06\/HALF-1-1-1024x415.png\" alt=\"\" class=\"wp-image-9316\" srcset=\"https:\/\/czecrin.cz\/wp-content\/uploads\/2022\/06\/HALF-1-1-980x397.png 980w, https:\/\/czecrin.cz\/wp-content\/uploads\/2022\/06\/HALF-1-1-480x194.png 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:\/\/redcap.med.muni.cz\/\" target=\"_blank\" rel=\"noreferrer noopener\">Access to REDCap database (for examiners)<\/a><\/strong><\/td><td class=\"has-text-align-center\" data-align=\"center\"><strong><a href=\"https:\/\/clinicaltrials.gov\/ct2\/show\/NCT04663555\" target=\"_blank\" rel=\"noreferrer noopener\">KH registration on ClinicalTrials.gov<\/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\"><a href=\"https:\/\/czecrin.cz\/wp-content\/uploads\/2025\/04\/HALF_stanovisko-MEK.pdf\" target=\"_blank\" rel=\"noreferrer noopener\"><strong>Approval of KH MEK FN Brno<\/strong><\/a><\/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<p class=\"has-text-align-center has-medium-font-size\">If you are interested in the full version of the ICF, or other KH documentation, please contact <a href=\"mailto:rychlickova@med.muni.cz\">rychlickova@med.muni.cz<\/a><\/p>\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\">National coordinator of the HALF study:<br>doc. MUDr. Daniela \u017d\u00e1\u010dkov\u00e1, Ph.D. | <a href=\"mailto:zackova.daniela@fnbrno.cz\">zackova.daniela@fnbrno.cz<\/a> | <a href=\"tel:+420532232838\">+420 532 232 838<\/a>   <\/p>\n\n\n\n<div style=\"height:20px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<p class=\"has-text-align-center has-medium-font-size\">Project managers:<br>PharmDr. Jitka Rychl\u00ed\u010dkov\u00e1, Ph.D., BCPS | <a href=\"mailto:rychlickova@med.muni.cz\">rychlickova@med.muni.cz<\/a><br>PharmDr. Ad\u00e9la B\u00e1rtov\u00e1 | <a href=\"mailto:adela.bartova@med.muni.cz\">adela.bartova@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%20HALF%20-%20Czecrin&#038;url=https%3A%2F%2Fczecrin.cz%2Fprojekty%2Fkh-half%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 HALF Prospective phase II clinical trial evaluating the efficacy and safety of tyrosine kinase inhibitor discontinuation after prior two-step dose reduction in patients with chronic myeloid leukemia in deep molecular remission The HALF clinical trial is designed as a prospective, multicentre, non-randomised, open-label phase II study to assess the efficacy and safety of [&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":[159,150],"class_list":["post-9062","project","type-project","status-publish","hentry","project_category-national-research-projects","project_category-ongoing-clinical-trials","project_tag-hematology","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 HALF &#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. 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