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author Михаил Исаакович Ликстанов
Ирина Николаевна Кушнир
Анна Владимировна Ромасюк
Ирина Анатольевна Хмелева
Екатерина Александровна Власова
Мария Сергеевна Маталасова
Татьяна Владимировна Шофорусь
Мария Геннадьевна Якушенко
Елена Владимировна Стрельцова
Павел Аскандерович Аскандеров
Вадим Гельевич Мозес
Евгения Юрьевна Рисовер
Елена Владимировна Рудаева
Светлана Ивановна Елгина
Кира Борисовна Мозес
author_facet Михаил Исаакович Ликстанов
Ирина Николаевна Кушнир
Анна Владимировна Ромасюк
Ирина Анатольевна Хмелева
Екатерина Александровна Власова
Мария Сергеевна Маталасова
Татьяна Владимировна Шофорусь
Мария Геннадьевна Якушенко
Елена Владимировна Стрельцова
Павел Аскандерович Аскандеров
Вадим Гельевич Мозес
Евгения Юрьевна Рисовер
Елена Владимировна Рудаева
Светлана Ивановна Елгина
Кира Борисовна Мозес
author_sort Михаил Исаакович Ликстанов
collection DOAJ
description The efficacy and safety of therapy with a human monoclonal antibody (international patent name Regdanvimab) in patients with a moderate course of COVID-19 was evaluated. A total of 41 patients (48.8 % women and 51.2 % men) were treated during the period of mixed distribution of delta and omicron strains of SARS-CoV-2. Regdanvimab was administered in a hospital setting based on the calculation of the amount of 40 mg/kg per patient's body weight. The median dose of regdanvimab was 3200 (2720; 4000) mg, the minimum dose was 2040 mg, and the maximum dose was 4800 mg. When prescribing regdanvimab, on the second day there was an improvement in the clinical picture and laboratory parameters characterizing the course of the infectious process. The lethality of patients during the study was due to the severity of the course of concomitant diseases and emphasizes the need for an integrated approach to the management of comorbid patients with the involvement of specialists from related fields, such as nephrologists, oncologists, chemotherapists, cardiologists, etc., in prescribing therapy. Thus, Regdanvimab proved the efficacy and safety of use in patients with COVID-19 during routine practice, while the clinical efficacy of the drug was shown in a mixed cohort of delta-omicron strains.
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spelling doaj.art-c9c41a07b8ef40329ec7208ab50205fc2023-05-05T11:35:19ZrusThe Publishing House Medicine and EnlightenmentMedicina v Kuzbasse1819-09012588-04112023-02-012211721754EFFICACY AND SAFETY OF REGDANVIMAB THERAPY IN MODERATE COURSE OF COVID-19Михаил Исаакович Ликстанов0Ирина Николаевна Кушнир1Анна Владимировна Ромасюк2Ирина Анатольевна Хмелева3Екатерина Александровна Власова4Мария Сергеевна Маталасова5Татьяна Владимировна Шофорусь6Мария Геннадьевна Якушенко7Елена Владимировна Стрельцова8Павел Аскандерович Аскандеров9Вадим Гельевич Мозес10Евгения Юрьевна Рисовер11Елена Владимировна Рудаева12Светлана Ивановна Елгина13Кира Борисовна Мозес14ГАУЗ КОКБ им. С.В. Беляева, г. КемеровоГАУЗ КОКБ им. С.В. Беляева, г. КемеровоГАУЗ КОКБ им. С.В. Беляева, г. КемеровоГАУЗ КОКБ им. С.В. Беляева, г. КемеровоГАУЗ КОКБ им. С.В. Беляева, г. КемеровоГАУЗ КОКБ им. С.В. Беляева, г. КемеровоГАУЗ КОКБ им. С.В. Беляева, г. КемеровоГАУЗ КОКБ им. С.В. Беляева, г. КемеровоГАУЗ КОКБ им. С.В. Беляева, г. КемеровоГАУЗ КОКБ им. С.В. Беляева, г. КемеровоФГБОУ ВО КемГУ, г. КемеровоКузбасская областная клиническая больница имени С.В. Беляева, г. КемеровоФГБОУ ВО КемГМУ Минздрава России, г. КемеровоФГБОУ ВО КемГМУ Минздрава России, г. КемеровоФГБОУ ВО КемГМУ Минздрава России, г. КемеровоThe efficacy and safety of therapy with a human monoclonal antibody (international patent name Regdanvimab) in patients with a moderate course of COVID-19 was evaluated. A total of 41 patients (48.8 % women and 51.2 % men) were treated during the period of mixed distribution of delta and omicron strains of SARS-CoV-2. Regdanvimab was administered in a hospital setting based on the calculation of the amount of 40 mg/kg per patient's body weight. The median dose of regdanvimab was 3200 (2720; 4000) mg, the minimum dose was 2040 mg, and the maximum dose was 4800 mg. When prescribing regdanvimab, on the second day there was an improvement in the clinical picture and laboratory parameters characterizing the course of the infectious process. The lethality of patients during the study was due to the severity of the course of concomitant diseases and emphasizes the need for an integrated approach to the management of comorbid patients with the involvement of specialists from related fields, such as nephrologists, oncologists, chemotherapists, cardiologists, etc., in prescribing therapy. Thus, Regdanvimab proved the efficacy and safety of use in patients with COVID-19 during routine practice, while the clinical efficacy of the drug was shown in a mixed cohort of delta-omicron strains.https://mednauki.ru/index.php/MK/article/view/852covid-19регданвимаблечение
spellingShingle Михаил Исаакович Ликстанов
Ирина Николаевна Кушнир
Анна Владимировна Ромасюк
Ирина Анатольевна Хмелева
Екатерина Александровна Власова
Мария Сергеевна Маталасова
Татьяна Владимировна Шофорусь
Мария Геннадьевна Якушенко
Елена Владимировна Стрельцова
Павел Аскандерович Аскандеров
Вадим Гельевич Мозес
Евгения Юрьевна Рисовер
Елена Владимировна Рудаева
Светлана Ивановна Елгина
Кира Борисовна Мозес
EFFICACY AND SAFETY OF REGDANVIMAB THERAPY IN MODERATE COURSE OF COVID-19
Medicina v Kuzbasse
covid-19
регданвимаб
лечение
title EFFICACY AND SAFETY OF REGDANVIMAB THERAPY IN MODERATE COURSE OF COVID-19
title_full EFFICACY AND SAFETY OF REGDANVIMAB THERAPY IN MODERATE COURSE OF COVID-19
title_fullStr EFFICACY AND SAFETY OF REGDANVIMAB THERAPY IN MODERATE COURSE OF COVID-19
title_full_unstemmed EFFICACY AND SAFETY OF REGDANVIMAB THERAPY IN MODERATE COURSE OF COVID-19
title_short EFFICACY AND SAFETY OF REGDANVIMAB THERAPY IN MODERATE COURSE OF COVID-19
title_sort efficacy and safety of regdanvimab therapy in moderate course of covid 19
topic covid-19
регданвимаб
лечение
url https://mednauki.ru/index.php/MK/article/view/852
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