Effect of Aprotinin and Avifavir® Combination Therapy for Moderate COVID-19 Patients

Author:

Ivashchenko Andrey A.,Azarova Valeria N.,Egorova Alina N.ORCID,Karapetian Ruben N.,Kravchenko Dmitry V.,Krivonos Natalia V.,Loginov Vladimir G.,Poyarkov Stanislav V.,Merkulova Elena A.,Rosinkova Olga S.,Savchuk Nikolay P.,Topr Mikhail A.,Simakina Elena N.,Yakubova Elena V.,Ivachtchenko Alexandre V.

Abstract

COVID-19 is a contagious multisystem inflammatory disease caused by a severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). We studied the efficacy of Aprotinin (nonspecific serine proteases inhibitor) in combination with Avifavir® or Hydroxychloroquine (HCQ) drugs, which are recommended by the Russian Ministry of Health for the treatment therapy of moderate COVID-19 patients. This prospective single-center study included participants with moderate COVID-19-related pneumonia, laboratory-confirmed SARS-CoV-2, and admitted to the hospitals. Patients received combinations of intravenous (IV) Aprotinin (1,000,000 KIU daily, 3 days) and HCQ (cohort 1), inhalation (inh) treatment with Aprotinin (625 KIU four times per day, 5 days) and HCQ (cohort 2) or IV Aprotinin (1,000,000 KIU daily for 5 days) and Avifavir (cohort 3). In cohorts 1–3, the combination therapy showed 100% efficacy in preventing the transfer of patients (n = 30) to the intensive care unit (ICU). The effect of the combination therapy in cohort 3 was the most prominent, and the median time to SARS-CoV-2 elimination was 3.5 days (IQR 3.0–4.0), normalization of the CRP concentration was 3.5 days (IQR 3–5), of the D-dimer concentration was 5 days (IQR 4 to 5); body temperature was 1 day (IQR 1–3), improvement in clinical status or discharge from the hospital was 5 days (IQR 5–5), and improvement in lung lesions of patients on 14 day was 100%.

Publisher

MDPI AG

Subject

Virology,Infectious Diseases

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