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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="en"><front><journal-meta><journal-id journal-id-type="publisher-id">akusherstvo</journal-id><journal-title-group><journal-title xml:lang="en">Obstetrics, Gynecology and Reproduction</journal-title><trans-title-group xml:lang="ru"><trans-title>Акушерство, Гинекология и Репродукция</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2313-7347</issn><issn pub-type="epub">2500-3194</issn><publisher><publisher-name>IRBIS LLC</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.17749/2313-7347/ob.gyn.rep.2024.500</article-id><article-id custom-type="elpub" pub-id-type="custom">akusherstvo-1999</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="en"><subject>REVIEW ARTICLES</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>НАУЧНЫЕ ОБЗОРЫ</subject></subj-group></article-categories><title-group><article-title>Reviewing the mechanism of action and results of clinical studies on the antifungal drug ibrexafungerp</article-title><trans-title-group xml:lang="ru"><trans-title>Обзор механизма действия и результатов клинических исследований противогрибкового препарата ибрексафунгерп</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-1734-3432</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Тагирова</surname><given-names>Л. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Tagirova</surname><given-names>L. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Лейсан Иршатовна Тагирова, ассистент</p><p>кафедра акушерства и гинекологии</p><p>450008; ул. Ленина, д. 3; Уфа</p></bio><bio xml:lang="en"><p>Leysan I. Tagirova, MD, Assistant</p><p>Department of Obstetrics and Gynecology</p><p>450008; 3 Lenin Str.; Ufa</p></bio><email xlink:type="simple">olofb@list.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/0000-0002-6434-1926</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Фарвазова</surname><given-names>К. Р.</given-names></name><name name-style="western" xml:lang="en"><surname>Farvazova</surname><given-names>K. R.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Камила Разифовна Фарвазова, студент</p><p>лечебный факультет</p><p>450008; ул. Ленина, д. 3; Уфа</p></bio><bio xml:lang="en"><p>Kamila R. Farvazova, Student</p><p>Faculty of General Medicine</p><p>450008; 3 Lenin Str.; Ufa</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-3217-6214</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Валеева</surname><given-names>Д. Р.</given-names></name><name name-style="western" xml:lang="en"><surname>Valeeva</surname><given-names>D. R.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Дания Рустемовна Валеева, студент</p><p>450008; ул. Ленина, д. 3; Уфа</p></bio><bio xml:lang="en"><p>Daniia R. Valeeva, Student</p><p>450008; 3 Lenin Str.; Ufa</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-0828-527X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Орлова</surname><given-names>М. Д.</given-names></name><name name-style="western" xml:lang="en"><surname>Orlova</surname><given-names>M. D.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Мария Дмитриевна Орлова, студент</p><p>педиатрический факультет</p><p>450008; ул. Ленина, д. 3; Уфа</p></bio><bio xml:lang="en"><p>Maria D. Orlova, Student</p><p>Faculty of Pediatrics</p><p>450008; 3 Lenin Str.; Ufa</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0004-2954-8456</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Губайдуллин</surname><given-names>И. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Gubaidullin</surname><given-names>I. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Ирик Азатович Губайдуллин, студент</p><p>лечебный факультет</p><p>450008; ул. Ленина, д. 3; Уфа</p></bio><bio xml:lang="en"><p>Irik A. Gubaidullin, Student</p><p>Faculty of General Medicine</p><p>450008; 3 Lenin Str.; Ufa</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-5021-1023</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Тулябаева</surname><given-names>А. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Tulyabaeva</surname><given-names>A. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Аделина Мурадымовна Тулябаева, студент</p><p>лечебный факультет</p><p>450008; ул. Ленина, д. 3; Уфа</p></bio><bio xml:lang="en"><p>Adelina M. Tulyabaeva, Student</p><p>Faculty of General Medicine</p><p>450008; 3 Lenin Str.; Ufa</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2089-3849</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Абдульманова</surname><given-names>А. Р.</given-names></name><name name-style="western" xml:lang="en"><surname>Abdulmanova</surname><given-names>A. R.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Айлина Робертовна Абдульманова, студент</p><p>лечебный факультет</p><p>450008; ул. Ленина, д. 3; Уфа</p></bio><bio xml:lang="en"><p>Ailina R. Abdulmanova, Student</p><p>Faculty of General Medicine</p><p>450008; 3 Lenin Str.; Ufa</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0005-9075-8898</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Тряпко</surname><given-names>Р. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Tryapko</surname><given-names>R. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Руслан Виталиевич Тряпко, ассистент</p><p>кафедра акушерства и гинекологии</p><p>344022; Нахичеванский переулок, д. 29; Ростов-на-Дону</p></bio><bio xml:lang="en"><p>Ruslan V. Tryapko, MD, Assistant</p><p>Department of Obstetrics and Gynecology</p><p>344022; 29 Nakhchivansky Lane; Rostov-on-Don</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0008-9732-252X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Шелыгинский</surname><given-names>Д. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Shelyginsky</surname><given-names>D. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Даниил Алексеевич Шелыгинский, студент</p><p>лечебный факультет</p><p>460000; ул. Советская, д. 6; Оренбург</p></bio><bio xml:lang="en"><p>Daniil A. Shelyginsky, Student</p><p>Faculty of General Medicine</p><p>460000; 6 Sovetskaya Str.; Orenburg</p></bio><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0002-7703-3989</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ханафиева</surname><given-names>А. Р.</given-names></name><name name-style="western" xml:lang="en"><surname>Khanafieva</surname><given-names>A. R.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Анжелика Романовна Ханафиева, студент</p><p>лечебный факультет</p><p>460000; ул. Советская, д. 6; Оренбург</p></bio><bio xml:lang="en"><p>Anzhelika R. Khanafieva, Student</p><p>Faculty of General Medicine</p><p>460000; 6 Sovetskaya Str.; Orenburg</p></bio><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-0085-2636</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Семенова</surname><given-names>Н. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Semenova</surname><given-names>N. G.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Настасья Генриховна Семенова, студент</p><p>лечебный факультет</p><p>450008; ул. Ленина, д. 3; Уфа</p></bio><bio xml:lang="en"><p>Nastasia G. Semenova, Student</p><p>Faculty of General Medicine</p><p>450008; 3 Lenin Str.; Ufa</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-8967-4903</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Такиуллин</surname><given-names>Э. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Takiullin</surname><given-names>E. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Эдуард Маратович Такиуллин, студент</p><p>лечебный факультет </p><p>450008; ул. Ленина, д. 3; Уфа</p></bio><bio xml:lang="en"><p>Eduard M. Takiullin, Student</p><p>Faculty of General Medicine</p><p>450008; 3 Lenin Str.; Ufa</p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБОУ ВО «Башкирский государственный медицинский университет» Министерства здравоохранения Российской Федерации</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Bashkir State Medical University, Health Ministry of Russian Federation</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>ФГБОУ ВО «Ростовский государственный медицинский университет» Министерства здравоохранения Российской Федерации</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Rostov State Medical University, Health Ministry of Russian Federation</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>ФГБОУ ВО «Оренбургский государственный медицинский университет» Министерства здравоохранения Российской Федерации</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Orenburg State Medical University, Health Ministry of Russian Federation</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2024</year></pub-date><pub-date pub-type="epub"><day>06</day><month>04</month><year>2024</year></pub-date><volume>18</volume><issue>2</issue><fpage>232</fpage><lpage>245</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Tagirova L.I., Farvazova K.R., Valeeva D.R., Orlova M.D., Gubaidullin I.A., Tulyabaeva A.M., Abdulmanova A.R., Tryapko R.V., Shelyginsky D.A., Khanafieva A.R., Semenova N.G., Takiullin E.M., 2024</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="ru">Тагирова Л.И., Фарвазова К.Р., Валеева Д.Р., Орлова М.Д., Губайдуллин И.А., Тулябаева А.М., Абдульманова А.Р., Тряпко Р.В., Шелыгинский Д.А., Ханафиева А.Р., Семенова Н.Г., Такиуллин Э.М.</copyright-holder><copyright-holder xml:lang="en">Tagirova L.I., Farvazova K.R., Valeeva D.R., Orlova M.D., Gubaidullin I.A., Tulyabaeva A.M., Abdulmanova A.R., Tryapko R.V., Shelyginsky D.A., Khanafieva A.R., Semenova N.G., Takiullin E.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.gynecology.su/jour/article/view/1999">https://www.gynecology.su/jour/article/view/1999</self-uri><abstract><sec><title>   Introduction</title><p>   Introduction. Vulvovaginal candidiasis is an extremely common pathology of the female genital organs, leading to a long-term recurrent course and multiple complications. Although currently it is widely known about developing antibiotic resistance of bacterial pathogens, it is necessary to remember about similar phenomenon observed in other groups of infectious agents. In this regard, fungal infection also requires development of new therapeutic techniques and medicinal antifungal drugs, such as ibrexafungerp.</p></sec><sec><title>   Aim</title><p>   Aim: to analyze available publications revealing the mechanism of action, efficacy, antifungal spectrum and results of clinical trials for a new oral antifungal drug ibrexafungerp.</p></sec><sec><title>   Materials and Methods</title><p>   Materials and Methods. A search for publications in the electronic databases PubMed, eLibrary and ClinicalTrials.gov, published over the last 25 years was conducted using the following keywords in Russian and English: “candidiasis”, “vulvovaginal candidiasis”, “antifungal drugs”, “ibrexafungerp”, “clinical trials”, “mechanism of action”. Articles were assessed according to PRISMA guidelines. The titles and abstracts of identified publications were independently reviewed to retrieve relevant full text studies. After the selection procedure, 46 articles were included in the review.</p></sec><sec><title>   Results</title><p>   Results. This review provides information on the creation of the drug ibrexafungerp, its mechanism of action, the activity against a relatively wide range of pathogens, as well as the results from 13 ongoing and completed clinical trials in patients with fungal infection.</p></sec><sec><title>   Conclusion</title><p>   Conclusion. The analysis of ibrexafungerp-related clinical studies showed its good oral bioavailability, high antifungal efficacy, so that its one-day dosage may further eliminate a need for unnecessarily long hospitalization and complex dosing schedules, thereby increasing adherence to therapy and odds for treatment success.</p></sec></abstract><trans-abstract xml:lang="ru"><sec><title>   Введение</title><p>   Введение. Вульвовагинальный кандидоз – чрезвычайно распространенная патология женских половых органов, приводящая к длительному рецидивирующему течению и множеству осложнений. Хотя в наши дни широко известно о развитии резистентности бактериальных возбудителей к антибиотикам, не стоит забывать о подобном явлении и у других групп возбудителей инфекций. Так, грибковая инфекция также требует разработки новых терапевтических методик и медикаментозных противогрибковых препаратов, таких как ибрексафунгерп.</p></sec><sec><title>   Цель</title><p>   Цель: провести анализ литературы, раскрывающей механизм действия, эффективность, противогрибковый спектр и результаты клинических испытаний нового орального противогрибкового препарата ибрексафунгерп.</p></sec><sec><title>   Материалы и методы</title><p>   Материалы и методы. Проведен поиск публикаций в электронных базах данных PubMed, еLibrary и ClinicalTrials.gov, опубликованных за последние 25 лет. Поиск исследований проводился с использованием следующих ключевых слов на русском и английском языках: «кандидоз», «вульвовагинальный кандидоз», «противогрибковые препараты», «ибрексафунгерп», «клинические испытания», «механизм действия», «candidiasis», «vulvovaginal candidiasis», «antifungal drugs», «ibrexafungerp», «clinical trials», «mechanism of action». Оценка статей проводилась в соответствии с рекомендациями PRISMA. Авторы независимо друг от друга анализировали названия и аннотации идентифицированных публикаций, после чего извлекали полный текст релевантных исследований. После процедуры отбора в обзор было включено 46 статей.</p></sec><sec><title>   Результаты</title><p>   Результаты. В обзоре представлена информация о создании препарата ибрексафунгерп, его механизм действия, активность относительно широкого спектра возбудителей, а также результаты 13 продолжающихся и завершенных клинических исследований данного препарата у пациентов с грибковой инфекцией.</p></sec><sec><title>   Заключение</title><p>   Заключение. Проведенный анализ клинических исследований препарата ибрексафунгерп показал, что его хорошая пероральная биодоступность, высокая противогрибковая эффективность и однодневная дозировка в перспективе исключат необходимость в излишне длительной госпитализации и сложных графиках дозирования, тем самым увеличивая приверженность к терапии и вероятность успеха лечения.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>кандидоз</kwd><kwd>вульвовагинальный кандидоз</kwd><kwd>ибрексафунгерп</kwd><kwd>инвазивная грибковая инфекция</kwd><kwd>эхинокандины</kwd><kwd>азолы</kwd></kwd-group><kwd-group xml:lang="en"><kwd>candidiasis</kwd><kwd>vulvovaginal candidiasis</kwd><kwd>ibrexafungerp</kwd><kwd>invasive fungal infection</kwd><kwd>echinocandins</kwd><kwd>azoles</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Авторы заявляют об отсутствии финансовой поддержки</funding-statement><funding-statement xml:lang="en">The authors declare no funding</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">Willems H.M.E., Ahmed S.S., Liu J. et al. Vulvovaginal candidiasis: a current understanding and burning questions. J Fungi (Basel). 2020;6(1):27. doi: 10.3390/jof6010027.</mixed-citation><mixed-citation xml:lang="en">Willems H.M.E., Ahmed S.S., Liu J. et al. Vulvovaginal candidiasis: a current understanding and burning questions. J Fungi (Basel). 2020;6(1):27. doi: 10.3390/jof6010027.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Гинекология: национальное руководство. Под ред. Г.М. Савельевой, Г.Т. Сухих, В.Н. Серова, В.Е. Радзинского, И.Б. Манухина. М.: ГЭОТАР-Медиа, 2022. 1008 с.</mixed-citation><mixed-citation xml:lang="en">Gynecology: national guidelines. Eds. G.M. Savelyeva, G.T. Sukhikh, V.N. Serova, V.E. Radzinsky, I.B. Manukhina. [Ginekologiya: nacional'noe rukovodstvo. Pod red. G.M. Savel'evoj, G.T. Suhih, V.N. Serova, V.E. Radzinskogo, I.B. Manuhina]. Moscow: GEOTAR-Media, 2022. 1008 p. (In Russ.).</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Хамадьянова А.У., Загидулина А.Р., Загретдинова Д.Р. и др. Перспективы исследования микробиома организма человека для лучшего понимания патогенеза рака яичников. Российский вестник акушера-гинеколога. 2023;23(1):39–46. doi: 10.17116/rosakush20232301139.</mixed-citation><mixed-citation xml:lang="en">Khamad’yanova A.U., Zagidulina A.R., Zagretdinova D.R. et al. Prospects of human microbiome study for better understanding of ovarian cancer pathogenesis. [Perspektivy issledovaniya mikrobioma organizma cheloveka dlya luchshego ponimaniya patogeneza raka yaichnikov]. Rossiiskii vestnik akushera-ginekologa. 2023;23(1):39–46. (In Russ.). doi: 10.17116/rosakush20232301139.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Байрамова Г.Р., Амирханян А.С., Чернова В.Ф. Вульвовагинальный кандидоз: патогенез, диагностика и тактика лечения. Доктор.Ру. 2018;(10):32–6. doi: 10.31550/1727-2378-2018-154-10-32-36.</mixed-citation><mixed-citation xml:lang="en">Bairamova G.R., Amirkhanyan A.S., Chernova V.F. Vulvovaginal candidiasis: pathogenesis, diagnosis and treatment strategy. [Vul'vovaginal'nyj kandidoz: patogenez, diagnostika i taktika lecheniya]. https://journaldoctor.ru/. 2018;(10):32–6. (In Russ.). doi: 10.31550/1727-2378-2018-154-10-32-36.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Зиганшин А.М., Мулюков А.Р. Механизмы иммунопатологии сепсиса вирусной этиологии при COVID-19. Сибирское медицинское обозрение. 2021;(6):35–43. doi: 10.20333/25000136-2021-6-35-43.</mixed-citation><mixed-citation xml:lang="en">Ziganshin A.M., Mulyukov A.R. Immunopathological mechanisms in sepsis of viral etiology in COVID-19. [Mekhanizmy immunopatologii sepsisa virusnoj etiologii pri COVID-19]. Sibirskoe medicinskoe obozrenie. 2021;(6):35–43. (In Russ.). doi: 10.20333/25000136-2021-6-35-43.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Зиганшин А.М., Кейдар С.В., Халитова Р.Ш. и др. Вирус папилломы человека: этиология, патогенез, роль и значение в развитии рака шейки матки. Гинекология. 2023;25(1):17–21. doi: 10.26442/20795696.2023.1.202070.</mixed-citation><mixed-citation xml:lang="en">Ziganshin A.M., Keidar S.V., Khalitova R.Sh. et al. Human papillomavirus: etiology, pathogenesis, role, and importance in the development of cervical cancer : a review. [Virus papillomy cheloveka: etiologiya, patogenez, rol' i znachenie v razvitii raka shejki matki]. Ginekologiya. 2023;25(1):17–21. (In Russ.). doi: 10.26442/20795696.2023.1.202070.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Qin F., Wang Q., Zhang C. et al. Efficacy of antifungal drugs in the treatment of vulvovaginal candidiasis: a Bayesian network meta-analysis. Infect Drug Resist. 2018;11:1893–901. doi: 10.2147/IDR.S175588.</mixed-citation><mixed-citation xml:lang="en">Qin F., Wang Q., Zhang C. et al. Efficacy of antifungal drugs in the treatment of vulvovaginal candidiasis: a Bayesian network meta-analysis. Infect Drug Resist. 2018;11:1893–901. doi: 10.2147/IDR.S175588.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Je N.K., Youm S., Chun P. Real world co-prescribing contraindicated drugs with fluconazole and itraconazole. Pharmacoepidemiol Drug Saf. 2023;32(7):752–62. doi: 10.1002/pds.5604.</mixed-citation><mixed-citation xml:lang="en">Je N.K., Youm S., Chun P. Real world co-prescribing contraindicated drugs with fluconazole and itraconazole. Pharmacoepidemiol Drug Saf. 2023;32(7):752–62. doi: 10.1002/pds.5604.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Аполихина И.А., Байрамова Г.Р., Гомберг М.А. и др. Клинические рекомендации по диагностике и лечению заболеваний, сопровождающихся патологическими выделениями из половых путей женщин. М.: Российское общество акушеров-гинекологов, 2019. 57 с.</mixed-citation><mixed-citation xml:lang="en">Apolikhina I.A., Bairamova G.R., Gomberg M.A. et al. Clinical guidelines for the diagnosis and treatment of diseases accompanied by pathological discharge from femal genital tract. [Klinicheskie rekomendacii po diagnostike i lecheniyu zabolevanij, soprovozhdayushchihsya patologicheskimi vydeleniyami iz polovyh putej zhenshchin]. Moscow: Rossijskoe obshchestvo akusherov-ginekologov, 2019. 57 p. (In Russ.).</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Pappas P.G., Kauffman C.A., Andes D.R. et al. Clinical practice guideline for the management of candidiasis: 2016 update by the Infectious Diseases Society of America. Clin Infect Dis. 2016;62(4):e1–50. doi: 10.1093/cid/civ933.</mixed-citation><mixed-citation xml:lang="en">Pappas P.G., Kauffman C.A., Andes D.R. et al. Clinical practice guideline for the management of candidiasis: 2016 update by the Infectious Diseases Society of America. Clin Infect Dis. 2016;62(4):e1–50. doi: 10.1093/cid/civ933.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Collins L.M., Moore R., Sobel J.D. Prognosis and long-term outcome of women with idiopathic recurrent vulvovaginal candidiasis caused by Candida albicans. J Low Genit Tract Dis. 2020;24(1):48–52. doi: 10.1097/LGT.0000000000000496.</mixed-citation><mixed-citation xml:lang="en">Collins L.M., Moore R., Sobel J.D. Prognosis and long-term outcome of women with idiopathic recurrent vulvovaginal candidiasis caused by Candida albicans. J Low Genit Tract Dis. 2020;24(1):48–52. doi: 10.1097/LGT.0000000000000496.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Babic M., Hukic M. Candida albicans and non-albicans species as etiological agent of vaginitis in pregnant and non-pregnant women. Bosn J Basic Med Sci. 2010;10(1):89–97. doi: 10.17305/bjbms.2010.2744.</mixed-citation><mixed-citation xml:lang="en">Babic M., Hukic M. Candida albicans and non-albicans species as etiological agent of vaginitis in pregnant and non-pregnant women. Bosn J Basic Med Sci. 2010;10(1):89–97. doi: 10.17305/bjbms.2010.2744.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Mikamo H., Sato Y., Tamaya T. In vitro antifungal activity of FK463, a new water-soluble echinocandin-like lipopeptide. J Antimicrob Chemother. 2000;4</mixed-citation><mixed-citation xml:lang="en">Mikamo H., Sato Y., Tamaya T. In vitro antifungal activity of FK463, a new water-soluble echinocandin-like lipopeptide. J Antimicrob Chemother. 2000;46(3):485–7. doi: 10.1093/jac/46.3.485.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Denning D.W. Echinocandin antifungal drugs. Lancet. 2003;362(9390):1142–51. doi: 10.1016/S0140-6736(03)14472-8.</mixed-citation><mixed-citation xml:lang="en">Denning D.W. Echinocandin antifungal drugs. Lancet. 2003;362(9390):1142–51. doi: 10.1016/S0140-6736(03)14472-8.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Peláez F., Cabello A., Platas G. et al. The discovery of enfumafungin, a novel antifungal compound produced by an endophytic Hormonema species biological activity and taxonomy of the producing organisms. Syst Appl Microbiol. 2000;23(3):333–43. doi: 10.1016/s0723-2020(00)80062-4.</mixed-citation><mixed-citation xml:lang="en">Peláez F., Cabello A., Platas G. et al. The discovery of enfumafungin, a novel antifungal compound produced by an endophytic Hormonema species biological activity and taxonomy of the producing organisms. Syst Appl Microbiol. 2000;23(3):333–43. doi: 10.1016/s0723-2020(00)80062-4.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Onishi J., Meinz M., Thompson J. et al. Discovery of novel antifungal (1,3)-beta-D-glucan synthase inhibitors. Antimicrob Agents Chemother. 2000;44(2):368–77. doi: 10.1128/AAC.44.2.368-377.2000.</mixed-citation><mixed-citation xml:lang="en">Onishi J., Meinz M., Thompson J. et al. Discovery of novel antifungal (1,3)-beta-D-glucan synthase inhibitors. Antimicrob Agents Chemother. 2000;44(2):368–77. doi: 10.1128/AAC.44.2.368-377.2000.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Apgar J.M., Wilkening R.R., Parker D.L. et al. Ibrexafungerp: an orally active β-1,3-glucan synthesis inhibitor. Bioorg Med Chem Lett. 2021;32:127661. doi: 10.1016/j.bmcl.2020.127661.</mixed-citation><mixed-citation xml:lang="en">Apgar J.M., Wilkening R.R., Parker D.L. et al. Ibrexafungerp: an orally active β-1,3-glucan synthesis inhibitor. Bioorg Med Chem Lett. 2021;32:127661. doi: 10.1016/j.bmcl.2020.127661.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Davis M.R., Donnelley M.A., Thompson G.R. Ibrexafungerp: a novel oral glucan synthase inhibitor. Med Mycol. 2020;58(5):579–92. doi: 10.1093/mmy/myz083.</mixed-citation><mixed-citation xml:lang="en">Davis M.R., Donnelley M.A., Thompson G.R. Ibrexafungerp: a novel oral glucan synthase inhibitor. Med Mycol. 2020;58(5):579–92. doi: 10.1093/mmy/myz083.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">SCYNEXIS Announces FDA Approval of Second Indication for BREXAFEMME® (ibrexafungerp tablets) for Reduction in Incidence of Recurrent Vulvovaginal Candidiasis. Режим доступа: https://ir.scynexis.com/news-events/press-releases/detail/314/scynexis-announces-fda-approval-of-second-indication-for. [Дата обращения: 01. 05. 2023].</mixed-citation><mixed-citation xml:lang="en">SCYNEXIS Announces FDA Approval of Second Indication for BREXAFEMME® (ibrexafungerp tablets) for Reduction in Incidence of Recurrent Vulvovaginal Candidiasis. Available at: https://ir.scynexis.com/news-events/press-releases/detail/314/scynexis-announces-fda-approval-of-second-indication-for. [Accessed: 01. 05. 2023].</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Garcia-Rubio R., de Oliveira H.C., Rivera J., Trevijano-Contador N. et al. The fungal cell wall: Candida, Cryptococcus, and Aspergillus species. Front Microbiol. 2020;10:2993. doi: 10.3389/fmicb.2019.02993.</mixed-citation><mixed-citation xml:lang="en">Garcia-Rubio R., de Oliveira H.C., Rivera J., Trevijano-Contador N. et al. The fungal cell wall: Candida, Cryptococcus, and Aspergillus species. Front Microbiol. 2020;10:2993. doi: 10.3389/fmicb.2019.02993.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Ghannoum M., Arendrup M.C., Chaturvedi V.P. et al. Ibrexafungerp: a novel oral triterpenoid antifungal in development for the treatment of Candida auris infections. Antibiotics (Basel). 2020;9(9):539. doi: 10.3390/antibiotics9090539.</mixed-citation><mixed-citation xml:lang="en">Ghannoum M., Arendrup M.C., Chaturvedi V.P. et al. Ibrexafungerp: a novel oral triterpenoid antifungal in development for the treatment of Candida auris infections. Antibiotics (Basel). 2020;9(9):539. doi: 10.3390/antibiotics9090539.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Hu X., Yang P., Chai C. et al. Structural and mechanistic insights into fungal β-1,3-glucan synthase FKS1. Nature. 2023;616(7955):190–8. doi: 10.1038/s41586-023-05856-5.</mixed-citation><mixed-citation xml:lang="en">Hu X., Yang P., Chai C. et al. Structural and mechanistic insights into fungal β-1,3-glucan synthase FKS1. Nature. 2023;616(7955):190–8. doi: 10.1038/s41586-023-05856-5.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Xie J.L., Grahl N., Sless T. et al. Signaling through Lrg1, Rho1 and Pkc1 governs Candida albicans morphogenesis in response to diverse cues. PLoS Genet. 2016;12(10):e1006405. doi: 10.1371/journal.pgen.1006405.</mixed-citation><mixed-citation xml:lang="en">Xie J.L., Grahl N., Sless T. et al. Signaling through Lrg1, Rho1 and Pkc1 governs Candida albicans morphogenesis in response to diverse cues. PLoS Genet. 2016;12(10):e1006405. doi: 10.1371/journal.pgen.1006405.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Latgé J.P. The cell wall: a carbohydrate armour for the fungal cell. Mol Microbiol. 2007;66(2):279–90. doi: 10.1111/j.1365-2958.2007.05872.x.</mixed-citation><mixed-citation xml:lang="en">Latgé J.P. The cell wall: a carbohydrate armour for the fungal cell. Mol Microbiol. 2007;66(2):279–90. doi: 10.1111/j.1365-2958.2007.05872.x.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Scorneaux B., Angulo D., Borroto-Esoda K. et al. SCY-078 is fungicidal against Candida species in time-kill studies. Antimicrob Agents Chemother. 2017;61(3):e01961–16. doi: 10.1128/AAC.01961-16.</mixed-citation><mixed-citation xml:lang="en">Scorneaux B., Angulo D., Borroto-Esoda K. et al. SCY-078 is fungicidal against Candida species in time-kill studies. Antimicrob Agents Chemother. 2017;61(3):e01961–16. doi: 10.1128/AAC.01961-16.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Ghannoum M., Long L., Larkin E.L. et al. Evaluation of the antifungal activity of the novel oral glucan synthase inhibitor SCY-078, singly and in combination, for the treatment of invasive Aspergillosis. Antimicrob Agents Chemother. 2018;62(6):e00244–18. doi: 10.1128/AAC.00244-18.</mixed-citation><mixed-citation xml:lang="en">Ghannoum M., Long L., Larkin E.L. et al. Evaluation of the antifungal activity of the novel oral glucan synthase inhibitor SCY-078, singly and in combination, for the treatment of invasive Aspergillosis. Antimicrob Agents Chemother. 2018;62(6):e00244–18. doi: 10.1128/AAC.00244-18.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Park S., Kelly R., Kahn J.N. et al. Specific substitutions in the echinocandin target Fks1p account for reduced susceptibility of rare laboratory and clinical Candida sp. isolates. Antimicrob Agents Chemother. 2005;49(8):3264-73. doi: 10.1128/AAC.49.8.3264-3273.2005.</mixed-citation><mixed-citation xml:lang="en">Park S., Kelly R., Kahn J.N. et al. Specific substitutions in the echino-candin target Fks1p account for reduced susceptibility of rare laboratory and clinical Candida sp. isolates. Antimicrob Agents Chemother. 2005;49(8):3264-73. doi: 10.1128/AAC.49.8.3264-3273.2005.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Marcos-Zambrano L.J., Gómez-Perosanz M., Escribano P. et al. The novel oral glucan synthase inhibitor SCY-078 shows in vitro activity against sessile and planktonic Candida spp. J Antimicrob Chemother. 2017;72(7):1969–76. doi: 10.1093/jac/dkx010.</mixed-citation><mixed-citation xml:lang="en">Marcos-Zambrano L.J., Gómez-Perosanz M., Escribano P. et al. The novel oral glucan synthase inhibitor SCY-078 shows in vitro activity against sessile and planktonic Candida spp. J Antimicrob Chemother. 2017;72(7):1969–76. doi: 10.1093/jac/dkx010.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Garcia-Effron G., Lee S., Park S. et al. Effect of Candida glabrata FKS1 and FKS2 mutations on echinocandin sensitivity and kinetics of 1,3-beta-D-glucan synthase: implication for the existing susceptibility breakpoint. Antimicrob Agents Chemother. 2009;53(9):3690–9. doi: 10.1128/AAC.00443-09.</mixed-citation><mixed-citation xml:lang="en">Garcia-Effron G., Lee S., Park S. et al. Effect of Candida glabrata FKS1 and FKS2 mutations on echinocandin sensitivity and kinetics of 1,3-beta-D-glucan synthase: implication for the existing susceptibility breakpoint. Antimicrob Agents Chemother. 2009;53(9):3690–9. doi: 10.1128/AAC.00443-09.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Schell W.A., Jones A.M., Borroto-Esoda K. et al. Antifungal activity of SCY-078 and standard antifungal agents against 178 clinical isolates of resistant and susceptible Candida species. Antimicrob Agents Chemother. 2017;61(11):e01102–17. doi: 10.1128/AAC.01102-17.</mixed-citation><mixed-citation xml:lang="en">Schell W.A., Jones A.M., Borroto-Esoda K. et al. Antifungal activity of SCY-078 and standard antifungal agents against 178 clinical isolates of resistant and susceptible Candida species. Antimicrob Agents Chemother. 2017;61(11):e01102–17. doi: 10.1128/AAC.01102-17.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Pfaller M.A., Messer S.A., Rhomberg P.R. et al. Differential activity of the oral glucan synthase inhibitor SCY-078 against wild-type and echinocandin-resistant strains of Candida species. Antimicrob Agents Chemother. 2017;61(8):e00161–17. doi: 10.1128/AAC.00161-17.</mixed-citation><mixed-citation xml:lang="en">Pfaller M.A., Messer S.A., Rhomberg P.R. et al. Differential activity of the oral glucan synthase inhibitor SCY-078 against wild-type and echinocandin-resistant strains of Candida species. Antimicrob Agents Chemother. 2017;61(8):e00161–17. doi: 10.1128/AAC.00161-17.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Berkow E.L., Angulo D., Lockhart S.R. In vitro activity of a novel glucan synthase inhibitor, SCY-078, against clinical isolates of Candida auris. Antimicrob Agents Chemother. 2017;61(7):e00435–17. doi: 10.1128/AAC.00435-17.</mixed-citation><mixed-citation xml:lang="en">Berkow E.L., Angulo D., Lockhart S.R. In vitro activity of a novel glucan synthase inhibitor, SCY-078, against clinical isolates of Candida auris. Antimicrob Agents Chemother. 2017;61(7):e00435–17. doi: 10.1128/AAC.00435-17.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Zhu Y.C., Barat S.A., Borroto-Esoda K. et al. Pan-resistant Candida auris isolates from the outbreak in New York are susceptible to ibrexafungerp (a glucan synthase inhibitor). Int J Antimicrob Agents. 2020;55(4):105922. doi: 10.1016/j.ijantimicag.2020.105922.</mixed-citation><mixed-citation xml:lang="en">Zhu Y.C., Barat S.A., Borroto-Esoda K. et al. Pan-resistant Candida auris isolates from the outbreak in New York are susceptible to ibrexafungerp (a glucan synthase inhibitor). Int J Antimicrob Agents. 2020;55(4):105922. doi: 10.1016/j.ijantimicag.2020.105922.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Jiménez-Ortigosa C., Paderu P., Motyl M.R., Perlin D.S. Enfumafungin derivative MK-3118 shows increased in vitro potency against clinical echinocandin-resistant Candida species and Aspergillus species isolates. Antimicrob Agents Chemother. 2014;58(2):1248–51. doi: 10.1128/AAC.02145-13.</mixed-citation><mixed-citation xml:lang="en">Jiménez-Ortigosa C., Paderu P., Motyl M.R., Perlin D.S. Enfumafungin derivative MK-3118 shows increased in vitro potency against clinical echinocandin-resistant Candida species and Aspergillus species isolates. Antimicrob Agents Chemother. 2014;58(2):1248–51. doi: 10.1128/AAC.02145-13.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Astvad K.M.T., Hare R.K., Arendrup M.C. Evaluation of the in vitro activity of isavuconazole and comparator voriconazole against 2635 contemporary clinical Candida and Aspergillus isolates. Clin Microbiol Infect. 2017;23(11):882–7. doi: 10.1016/j.cmi.2017.03.023.</mixed-citation><mixed-citation xml:lang="en">Astvad K.M.T., Hare R.K., Arendrup M.C. Evaluation of the in vitro activity of isavuconazole and comparator voriconazole against 2635 contemporary clinical Candida and Aspergillus isolates. Clin Microbiol Infect. 2017;23(11):882–7. doi: 10.1016/j.cmi.2017.03.023.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Pfaller M.A., Messer S.A., Motyl M.R. et al. In vitro activity of a new oral glucan synthase inhibitor (MK-3118) tested against Aspergillus spp. by CLSI and EUCAST broth microdilution methods. Antimicrob Agents Chemother. 2013;57(2):1065–8. doi: 10.1128/AAC.01588-12.</mixed-citation><mixed-citation xml:lang="en">Pfaller M.A., Messer S.A., Motyl M.R. et al. In vitro activity of a new oral glucan synthase inhibitor (MK-3118) tested against Aspergillus spp. by CLSI and EUCAST broth microdilution methods. Antimicrob Agents Chemother. 2013;57(2):1065–8. doi: 10.1128/AAC.01588-12.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Lamoth F., Alexander B.D. Antifungal activities of SCY-078 (MK-3118) and standard antifungal agents against clinical non-Aspergillus mold isolates. Antimicrob Agents Chemother. 2015;59(7):4308–11. doi: 10.1128/AAC.00234-15.</mixed-citation><mixed-citation xml:lang="en">Lamoth F., Alexander B.D. Antifungal activities of SCY-078 (MK-3118) and standard antifungal agents against clinical non-Aspergillus mold isolates. Antimicrob Agents Chemother. 2015;59(7):4308–11. doi: 10.1128/AAC.00234-15.</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Wring S., Murphy G., Atiee G. et al. Clinical pharmacokinetics and drug-drug interaction potential for coadministered SCY-078, an oral fungicidal glucan synthase inhibitor, and tacrolimus. Clin Pharmacol Drug Dev. 2019;8(1):60–9. doi: 10.1002/cpdd.588.</mixed-citation><mixed-citation xml:lang="en">Wring S., Murphy G., Atiee G. et al. Clinical pharmacokinetics and drug-drug interaction potential for coadministered SCY-078, an oral fungicidal glucan synthase inhibitor, and tacrolimus. Clin Pharmacol Drug Dev. 2019;8(1):60–9. doi: 10.1002/cpdd.588.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Wring S.A., Randolph R., Park S. et al. Preclinical pharmacokinetics and pharmacodynamic target of SCY-078, a first-in-class orally active antifungal glucan synthesis inhibitor, in murine models of disseminated candidiasis. Antimicrob Agents Chemother. 2017;61(4):e02068–16. doi: 10.1128/AAC.02068-16.</mixed-citation><mixed-citation xml:lang="en">Wring S.A., Randolph R., Park S. et al. Preclinical pharmacokinetics and pharmacodynamic target of SCY-078, a first-in-class orally active antifungal glucan synthesis inhibitor, in murine models of disseminated candidiasis. Antimicrob Agents Chemother. 2017;61(4):e02068–16. doi: 10.1128/AAC.02068-16.</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Wring S., Borroto-Esoda K., Solon E., Angulo D. SCY-078, a novel fungicidal agent, demonstrates distribution to tissues associated with fungal infections during mass balance studies with intravenous and oral [14C]SCY-078 in albino and pigmented rats. Antimicrob Agents Chemother. 2019;63(2):e02119–18. doi: 10.1128/AAC.02119-18.</mixed-citation><mixed-citation xml:lang="en">Wring S., Borroto-Esoda K., Solon E., Angulo D. SCY-078, a novel fungicidal agent, demonstrates distribution to tissues associated with fungal infections during mass balance studies with intravenous and oral [14C]SCY-078 in albino and pigmented rats. Antimicrob Agents Chemother. 2019;63(2):e02119–18. doi: 10.1128/AAC.02119-18.</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Lepak A.J., Marchillo K., Andes D.R. Pharmacodynamic target evaluation of a novel oral glucan synthase inhibitor, SCY-078 (MK-3118), using an in vivo murine invasive candidiasis model. Antimicrob Agents Chemother. 2015;59(2):1265–72. doi: 10.1128/AAC.04445-14.</mixed-citation><mixed-citation xml:lang="en">Lepak A.J., Marchillo K., Andes D.R. Pharmacodynamic target evaluation of a novel oral glucan synthase inhibitor, SCY-078 (MK-3118), using an in vivo murine invasive candidiasis model. Antimicrob Agents Chemother. 2015;59(2):1265–72. doi: 10.1128/AAC.04445-14.</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Spec A., Pullman J., Thompson G.R. et al. MSG-10: a Phase 2 study of oral ibrexafungerp (SCY-078) following initial echinocandin therapy in non-neutropenic patients with invasive candidiasis. J Antimicrob Chemother. 2019;74(10):3056–62. URL: https://pubmed.ncbi.nlm.nih.gov/31304536/..</mixed-citation><mixed-citation xml:lang="en">Spec A., Pullman J., Thompson G.R. et al. MSG-10: a Phase 2 study of oral ibrexafungerp (SCY-078) following initial echinocandin therapy in non-neutropenic patients with invasive candidiasis. J Antimicrob Chemother. 2019;74(10):3056–62. URL: https://pubmed.ncbi.nlm.nih.gov/31304536/.</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Cadet R., Tufa M., Angulo D., Nyirjesy P. A Phase 2b, dose-finding study evaluating oral Ibrexafungerp vs Fluconazole in vulvovaginal candidiasis (DOVE). Obstet Gynecol. 2019;133(1):113S–114S. doi: 10.1097/01.AOG.0000558840.33387.ee.</mixed-citation><mixed-citation xml:lang="en">Cadet R., Tufa M., Angulo D., Nyirjesy P. A Phase 2b, dose-finding study evaluating oral Ibrexafungerp vs Fluconazole in vulvovaginal candidiasis (DOVE). Obstet Gynecol. 2019;133(1):113S–114S. doi: 10.1097/01.AOG.0000558840.33387.ee.</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Goje O., Sobel R., Nyirjesy P. et al. Oral Ibrexafungerp for vulvovaginal candidiasis treatment: an analysis of VANISH 303 and VANISH 306. J Women Health. 2023;32(2):178–86. doi: 10.1089/jwh.2022.0132.</mixed-citation><mixed-citation xml:lang="en">Goje O., Sobel R., Nyirjesy P. et al. Oral Ibrexafungerp for vulvovaginal candidiasis treatment: an analysis of VANISH 303 and VANISH 306. J Women Health. 2023;32(2):178–86. doi: 10.1089/jwh.2022.0132.</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Scynexis SCYNEXIS Announces Positive Top-Line Results from Its Second Pivotal Phase 3 Study (VANISH-306) of Oral Ibrexafungerp for the Treatment of Vulvovaginal Candidiasis (Vaginal Yeast Infection). SCYNEXIS. Режим доступа: https://ir.scynexis.com/news-events/press-releases/detail/262/scynexis-pivotal-phase-3-vanish-306-trial-results-published. [Дата обращения: 01. 05. 2023].</mixed-citation><mixed-citation xml:lang="en">Scynexis SCYNEXIS Announces Positive Top-Line Results from Its Second Pivotal Phase 3 Study (VANISH-306) of Oral Ibrexafungerp for the Treatment of Vulvovaginal Candidiasis (Vaginal Yeast Infection). SCYNEXIS. Available at: https://ir.scynexis.com/news-events/press-releases/detail/262/scynexis-pivotal-phase-3-vanish-306-trial-results-published. [Accessed: 01. 05. 2023].</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Phillips N.A., Rocktashel M., Merjanian L. Ibrexafungerp for the treatment of vulvovaginal candidiasis: design, development and place in therapy. Drug Des Devel Ther. 2023;17:363–7. doi: 10.2147/DDDT.S339349.</mixed-citation><mixed-citation xml:lang="en">Phillips N.A., Rocktashel M., Merjanian L. Ibrexafungerp for the treatment of vulvovaginal candidiasis: design, development and place in therapy. Drug Des Devel Ther. 2023;17:363–7. doi: 10.2147/DDDT.S339349.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
