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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">10.30895/1991-2919-2024-14-3-351-361</article-id><article-id custom-type="elpub" pub-id-type="custom">vedomostiregmed-606</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>КЛИНИЧЕСКИЕ ИССЛЕДОВАНИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CLINICAL STUDIES</subject></subj-group></article-categories><title-group><article-title>Программа изучения лекарственных препаратов для лечения генерализованного тревожного расстройства: анализ Рекомендаций Европейского агентства по лекарственным средствам</article-title><trans-title-group xml:lang="en"><trans-title>Programme for Studying Medicinal Products for Generalised Anxiety Disorder: Analysis of the European Medicines Agency Guideline</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-9244-8934</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Соловьева</surname><given-names>А. П.</given-names></name><name name-style="western" xml:lang="en"><surname>Solovyova</surname><given-names>A. P.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Соловьева Анна Петровна, канд. мед. наук</p><p>Петровский бульвар, д. 8, стр. 2, Москва, 127051</p></bio><bio xml:lang="en"><p>Anna P. Solovyova, Cand. Sci. (Med.)</p><p>8/2 Petrovsky Blvd, Moscow 127051</p></bio><email xlink:type="simple">soloviova@expmed.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-9845-1018</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Сурмило</surname><given-names>И. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Surmilo</surname><given-names>I. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Сурмило Ирина Михайловна</p><p>Петровский бульвар, д. 8, стр. 2, Москва, 127051</p></bio><bio xml:lang="en"><p>Irina M. Surmilo</p><p>8/2 Petrovsky Blvd, Moscow 127051</p></bio><email xlink:type="simple">surmilo@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>2024</year></pub-date><pub-date pub-type="epub"><day>19</day><month>06</month><year>2024</year></pub-date><volume>14</volume><issue>3</issue><fpage>351</fpage><lpage>361</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Соловьева А.П., Сурмило И.М., 2024</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="ru">Соловьева А.П., Сурмило И.М.</copyright-holder><copyright-holder xml:lang="en">Solovyova A.P., Surmilo I.M.</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/606">https://www.vedomostincesmp.ru/jour/article/view/606</self-uri><abstract><sec><title>ВВЕДЕНИЕ</title><p>ВВЕДЕНИЕ. Генерализованное тревожное расстройство (ГТР) является наименее изученным из ряда тревожных расстройств ввиду наличия у пациентов сопутствующей патологии, связанной с расстройствами настроения. Поиск эффективных методов лечения ГТР является крайне важной задачей, что и обусловливает актуальность разработки новых лекарственных препаратов для лечения ГТР. Надлежащее планирование программы проведения клинических исследований является залогом получения достоверных данных об эффективности и безопасности лекарственных препаратов. В настоящий момент методическое руководство по проведению клинических исследований ГТР в Российской Федерации отсутствует и поставлена задача его разработки.</p></sec><sec><title>ЦЕЛЬ</title><p>ЦЕЛЬ. Оценка возможности использования методологических подходов зарубежных руководящих документов к проведению клинических исследований лекарственных средств в российской клинической практике при разработке лекарственных средств для терапии генерализованного тревожного расстройства.</p></sec><sec><title>ОБСУЖДЕНИЕ</title><p>ОБСУЖДЕНИЕ. Выполнен анализ основных положений Руководства по клиническим исследованиям препаратов для терапии ГТР Европейского агентства по лекарственным средствам (European Medicines Agency, EMA). Описаны основные этапы клинических исследований лекарственных препаратов и методология использования результатов этих исследований для оценки эффективности и безопасности данной группы препаратов. Показано, что при разработке программы клинических исследований ГТР необходимо учитывать этапность проведения исследований, обязательной является долгосрочная оценка безопасности и аддитивного эффекта. Выделены аспекты выбора дизайна клинических исследований, формирования групп исследований, а также определения первичных и вторичных конечных точек исследований. Особый акцент сделан на учете коморбидности пациентов.</p></sec><sec><title>ВЫВОДЫ</title><p>ВЫВОДЫ. Положения руководства ЕМА могут послужить основой отечественного руководства по изучению лекарственных препаратов для лечения генерализованного тревожного расстройства.</p></sec></abstract><trans-abstract xml:lang="en"><sec><title>INTRODUCTION</title><p>INTRODUCTION. Generalised anxiety disorder (GAD) is the least studied anxiety disorder, as patients present with comorbid mood disorders. Finding effective treatment methods for GAD is of the utmost importance; therefore, it is essential to develop novel medicinal products for GAD. Proper clinical programme design is key to obtaining reliable data on the effectiveness and safety of a medicinal product. Currently, the Russian Federation lacks methodological guidelines for clinical studies of these medcinal products, and there is a need for developing such guidelines.</p></sec><sec><title>AIM</title><p>AIM. This review aimed to assess the possibility of applying the methodological approaches described in international guidelines to Russian clinical trials to develop medicinal products for GAD.</p></sec><sec><title>DISCUSSION</title><p>DISCUSSION. Having analysed the main provisions of the Guideline on the clinical investigation of medicinal products indicated for generalised anxiety disorder by the European Medicines Agency (EMA), the authors of this review outlined the main stages of clinical development and the methodology for using clinical data to evaluate the safety and efficacy of medicinal products for GAD. Clinical development programmes for these medicinal products should take into account research staging and mandatory long-term safety and additive effect assessments. This review highlights aspects of selecting the design, population, and primary and secondary endpoints for a clinical trial. Particular attention is paid to the consideration of comorbidities in patients.</p></sec><sec><title>CONCLUSION</title><p>CONCLUSION. The provisions set forth in the EMA guideline can inform the development of national guidelines for studying medicinal products for GAD.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>генерализованное тревожное расстройство</kwd><kwd>клиническое исследование</kwd><kwd>дизайн исследования</kwd><kwd>коморбидность</kwd><kwd>психические расстройства</kwd><kwd>шкала тревоги Гамильтона</kwd><kwd>шкала общего клинического впечатления</kwd><kwd>шкала инвалидности Шихана</kwd><kwd>планирование клинического исследования</kwd><kwd>руководство ЕМA</kwd></kwd-group><kwd-group xml:lang="en"><kwd>generalised anxiety disorder</kwd><kwd>clinical trial</kwd><kwd>study design</kwd><kwd>co-morbidity</kwd><kwd>mental health issues</kwd><kwd>Hamilton Anxiety Rating Scale</kwd><kwd>Clinical Global Impression Scale</kwd><kwd>Sheehan Disability Scale</kwd><kwd>clinical trial planning</kwd><kwd>EMA guidelines</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Работа выполнена в рамках государственного задания ФГБУ «НЦЭСМП» Минздрава России № 056-00026-24-00 на проведение прикладных научных исследований (номер государственного учета НИР 124022300127-0).</funding-statement><funding-statement xml:lang="en">The study reported in this publication was carried out as part of publicly funded research project No. 056-00026-24-00 and was supported by the Scientific Centre for Expert Evaluation of Medicinal Products (R&amp;D reporting No. 124022300127-0).</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">Залуцкая НМ. 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