Третья фаза клинических испытаний (КИ) ингаляционного препарата «Лейтрагин», предотвращающего одно из тяжелых осложнений COVID-19 – цитокиновый шторм, показала эффективность разработки ФМБА России. Лекарство сокращает время выздоровления и продолжительности госпитализации в полтора раза, уверяют в пресс-службе ведомства.В ходе КИ удалось подтвердить и безопасность препарата: в группе пациентов, принимавших «Лейтрагин», не было зарегистрировано ни одного серьезного побочного эффекта.Минздрав РФ зарегистрировал разработку ФМБА России «Лейтрагин» 25 мая 2021 года. Ранее ученые экспериментально показали, что препарат способен снижать уровни HMGB1 при остром поражении легких, за счет чего предупреждает цитокиновый шторм.
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