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[Evaluation of the efficacy and safety of a complex antiviral drug based on antibodies in the treatment of adult patients with acute respiratory viral infection].
Khamitov, R F; Nikiforov, V V; Zaytsev, A A; Tragira, I N.
Afiliación
  • Khamitov RF; Kazan State Medical University.
  • Nikiforov VV; Pirogov Russian National Research Medical University.
  • Zaytsev AA; Federal Scientific and Clinical Center for Specialized Types of Medical Care and Medical Technologies.
  • Tragira IN; Burdenko Main Military Clinical Hospital.
Ter Arkh ; 94(1): 83-93, 2022 Jan 15.
Article en Ru | MEDLINE | ID: mdl-36286922
AIM: To evaluate the efficacy and safety of Raphamin, containing technologically processed affinity-purified antibodies to interferon , CD4 receptor, 1 domain of the major histocompatibility complex class II and 2 microglobulin major histocompatibility complex class I in the treatment of acute respiratory viral infection (ARVI), including influenza, in adults. MATERIALS AND METHODS: 240 patients 1870 years old with ARVI were included in a phase III (20192020), randomized, double-blind, placebo-controlled trial. Pregnant women, patients with suspected bacterial infections were excluded from the study. Raphamin/placebo was prescribed for 5 days within 24 hours of the illness onset. Primary endpoint was a time to resolution of ARVI (Polymerase chain reaction PCR-confirmed). Additionally, the severity of ARVI, proportion of patients with ARVI resolution/worsening/complications, frequency of antipyretics prescription, and time to resolution of symptoms of ARVI (including PCR non confirmed) were assessed. RESULTS: The average time to resolution of ARVI (PCR-confirmed) was 4.11.9 [4.01.9] and 5.02.5 [5.02.5] days in the Raphamin/placebo groups (ITT and [PP] analysis, р=0.0155 and [р=0.0114], respectively). The duration of ARVI decreased by 0.892.23 [0.932.25] days. Superiority of Raphamin was shown during therapy period according to the ARVI resolution criterion (р=0.0014 [р=0.0005]). There were no statistically significant difference in the severity of ARVI and frequency of antipyretics prescription. The proportion of patients with worsening/complications was 0 [0]% and 2.5 [2.8]% in the Raphamin and placebo groups, respectively. Favorable safety profile of Raphamin (including the incidence and severity of adverse events) and high compliance were shown. CONCLUSION: Raphamin promotes significant decrease, practically by a day, the duration of ARVI, including influenza.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Infecciones del Sistema Respiratorio / Virosis / Gripe Humana / Antipiréticos Tipo de estudio: Clinical_trials Límite: Adult / Female / Humans / Pregnancy Idioma: Ru Revista: Ter Arkh Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Infecciones del Sistema Respiratorio / Virosis / Gripe Humana / Antipiréticos Tipo de estudio: Clinical_trials Límite: Adult / Female / Humans / Pregnancy Idioma: Ru Revista: Ter Arkh Año: 2022 Tipo del documento: Article