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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">vedomostiregmed</journal-id><journal-title-group><journal-title xml:lang="ru">Регуляторные исследования и экспертиза лекарственных средств</journal-title><trans-title-group xml:lang="en"><trans-title>Regulatory Research and Medicine Evaluation</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">3034-3062</issn><issn pub-type="epub">3034-3453</issn><publisher><publisher-name>Federal State Budgetary Institution ‘Scientific Centre for Expert Evaluation of Medicinal Products’ of the Ministry of Health of the Russian Federation (FSBI ‘SCEEMP’)</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.30895/1991-2919-2021-11-2-202-211</article-id><article-id custom-type="elpub" pub-id-type="custom">vedomostiregmed-361</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>МЕТОДИЧЕСКИЕ МАТЕРИАЛЫ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>METHODICAL APPROACHES</subject></subj-group></article-categories><title-group><article-title>Планирование программы клинических исследований препаратов для лечения аксиального спондилоартрита</article-title><trans-title-group xml:lang="en"><trans-title>Planning a Clinical Trial Programme for Medicinal Products for the Treatment of Axial Spondyloarthritis</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-8583-2372</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Горячев</surname><given-names>Д. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Goryachev</surname><given-names>D. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Горячев Дмитрий Владимирович, д-р мед. наук,</p><p>Петровский б-р, д. 8, стр. 2, Москва, 127051</p></bio><bio xml:lang="en"><p>Dmitry V. Goryachev, Dr. Sci. (Med.),</p><p>8/2 Petrovsky Blvd, Moscow 127051 </p><p> </p></bio><email xlink:type="simple">Gorachev@expmed.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Федеральное государственное бюджетное учреждение «Научный центр экспертизы средств медицинского применения» Министерства здравоохранения Российской Федерации</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Scientific Centre for Expert Evaluation of Medicinal Products,</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2021</year></pub-date><pub-date pub-type="epub"><day>14</day><month>07</month><year>2021</year></pub-date><volume>11</volume><issue>3</issue><fpage>202</fpage><lpage>211</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Горячев Д.В., 2021</copyright-statement><copyright-year>2021</copyright-year><copyright-holder xml:lang="ru">Горячев Д.В.</copyright-holder><copyright-holder xml:lang="en">Goryachev D.V.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.vedomostincesmp.ru/jour/article/view/361">https://www.vedomostincesmp.ru/jour/article/view/361</self-uri><abstract><p>В последнее десятилетие критерии диагностики и классификация спондилоартритов претерпели существенные изменения. Появление новых диагностических методов и накопление информации по прогнозу исхода заболевания привели к выделению отдельной группы спондилоартритов – аксиального спондилоартрита. Выделение этого заболевания связано со специфическими механизмами его развития и высокой социальной значимостью. Разработка лекарственных препаратов, применяющихся при терапии больных аксиальным спондилоартритом, имеет ряд особенностей, что требует подготовки специальных рекомендаций для проведения клинических исследований лекарственных препаратов. Цель работы – формирование методического подхода к проведению клинических исследований и оценке эффективности и безопасности лекарственных средств для системного лечения аксиального спондилоартрита. Для гармонизации экспертной оценки результатов национальных и зарубежных клинических исследований работа была проведена с учетом требований/ рекомендаций Европейского агентства по лекарственным средствам по планированию клинических исследований лекарственных препаратов для лечения аксиального спондилоартрита. В работе выделены этапы клинических исследований, определены критерии оценки эффективности для каждого из этапов. Охарактеризованы методы и инструменты анализа конечных точек клинических исследований, необходимых для оценки влияния терапевтических воздействий. Описаны особенности дизайнов клинических исследований и длительность их проведения. Выделены задачи поисковых и подтверждающих клинических исследований. Рассмотрены цели лечения, показатели результатов лечения. Результаты исследования целесообразно использовать при разработке рекомендаций по программе клинического изучения новых препаратов для лечения аксиального спондилоартрита.</p></abstract><trans-abstract xml:lang="en"><p>The criteria for diagnosis and classification of spondyloarthritides (SpAs) have undergone significant changes over the past 10 years. The emergence of new diagnostic methods and availability of new information on the prognosis of the disease outcome made it possible to distinguish a separate group of SpAs—axial SpA. Axial SpA is distinguished as a separate disease due to its high social significance, and special mechanisms of its development. The development of medicinal products for the treatment of axial SpA has some specific features, which requires preparation of specific recommendations for conducting clinical trials of such products. The aim of the study was to elaborate a methodological approach to clinical research and evaluation of efficacy and safety of medicinal products for systemic treatment of axial SpA. The study took into account the requirements/recommendations of the European Medicines Agency for planning clinical trials of medicinal products for the treatment of axial SpA, in order to streamline evaluation of national and foreign clinical trial results. The paper identifies the main stages of clinical trials, and proposes criteria for assessing product efficacy at each stage. It defines methods and tools for assessing clinical trial endpoints, which are necessary for evaluation of treatment effects. The paper describes specific aspects of clinical trial designs and their duration, and identifies the objectives of exploratory and confirmatory clinical trials. It also reviews treatment goals and treatment outcome evaluation. The study results could be used in elaboration of recommendations for clinical research of new medicinal products for axial SpA.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>клиническое исследование</kwd><kwd>аксиальный спондилоартрит</kwd><kwd>анкилозирующий спондилит</kwd><kwd>первичная конечная точка</kwd><kwd>биологические лекарственные препараты</kwd><kwd>оценка эффективности и безопасности</kwd></kwd-group><kwd-group xml:lang="en"><kwd>clinical trial</kwd><kwd>axial spondyloarthrititis</kwd><kwd>ankylosing spondylitis</kwd><kwd>primary endpoint</kwd><kwd>biological medicinal products</kwd><kwd>efficacy and safety assessment</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Работа выполнена в рамках государственного задания ФГБУ «НЦЭСМП» Минздрава России № 056-00005-21-00 на проведение прикладных научных исследований (номер государственного учета НИР 121021800098-4).</funding-statement><funding-statement xml:lang="en">The study reported in this publication was carried out as part of a publicly funded research project No. 056-00005-21-00 and was supported by the Scientific Centre for Expert Evaluation of Medicinal Products (R&amp;D public accounting No. 121021800098-4).</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Эрдес ШФ, Бадокин ВВ, Бочкова АГ, Бугрова ОВ, Гайдукова ИЗ, Годзенко АА и др. 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