The Lancet Regional Health. Americas (Apr 2023)

Antivirals for adult patients hospitalised with SARS-CoV-2 infection: a randomised, phase II/III, multicentre, placebo-controlled, adaptive study, with multiple arms and stages. COALITION COVID-19 BRAZIL IX – REVOLUTIOn trialResearch in context

  • Israel S. Maia,
  • Aline Marcadenti,
  • Viviane C. Veiga,
  • Tamiris A. Miranda,
  • Samara P.C. Gomes,
  • Mariana B.S. Carollo,
  • Karina L. Negrelli,
  • Jackeline O. Gomes,
  • Lucas Tramujas,
  • Erlon O. Abreu-Silva,
  • Glauco A. Westphal,
  • Ruthy P. Fernandes,
  • Jacques G.A. Horta,
  • Deborah C. Oliveira,
  • Uri A.P. Flato,
  • Ricardo C.R. Paoliello,
  • Camilo Fernandes,
  • Cássio L. Zandonai,
  • Juliana C. Coelho,
  • Waldemar C. Barros,
  • Juliana C. Lemos,
  • Renata S. Bolan,
  • Marcela M. Dutra,
  • Otavio C.E. Gebara,
  • Ana T.A. Lopes,
  • Meton S. Alencar Filho,
  • Jussara A. Arraes,
  • Victor A. Hamamoto,
  • Mauro E. Hernandes,
  • Nicole A. Golin,
  • Tiago M. Santos,
  • Renato H.N. Santos,
  • Lucas P. Damiani,
  • Fernando G. Zampieri,
  • João Gesto,
  • Flávia R. Machado,
  • Régis G. Rosa,
  • Luciano C.P. Azevedo,
  • Alvaro Avezum,
  • Renato D. Lopes,
  • Thiago M.L. Souza,
  • Otávio Berwanger,
  • Alexandre B. Cavalcanti

Journal volume & issue
Vol. 20
p. 100466

Abstract

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Summary: Background: Repurposed drugs for treatment of new onset disease may be an effective therapeutic shortcut. We aimed to evaluate the efficacy of repurposed antivirals compared to placebo in lowering SARS-CoV2 viral load of COVID-19 patients. Methods: REVOLUTIOn is a randomised, parallel, blinded, multistage, superiority and placebo controlled randomised trial conducted in 35 centres in Brazil. We include patients aged 18 years or older admitted to hospital with laboratory-confirmed SARS-CoV-2 infection, symptoms onset 9 days or less and SpO2 94% or lower at room air were eligible. All participants were randomly allocated to receive either atazanavir, daclatasvir or sofosbuvir/daclatasvir or placebo for 10 days. The primary outcome was the decay rate (slope) of the SARS-CoV-2 viral load logarithm assessed in the modified intention to-treat population. This trial was registered with ClinicalTrials.gov, number NCT04468087. Findings: Between February 09, 2021, and August 04, 2021, 255 participants were enrolled and randomly assigned to atazanavir (n = 64), daclatasvir (n = 66), sofosbuvir/daclatasvir (n = 67) or placebo (n = 58). Compared to placebo group, the change from baseline to day 10 in log viral load was not significantly different for any of the treatment groups (0.05 [95% CI, −0.03 to 0.12], −0.02 [95% CI, −0.09 to 0.06], and −0.03 [95% CI, −0.11 to 0.04] for atazanavir, daclatasvir and sofosbuvir/daclatasvir groups respectively). There was no significant difference in the occurrence of serious adverse events between treatment groups. Interpretation: No significant reduction in viral load was observed from the use of atazanavir, daclatasvir or sofosbuvir/daclatasvir compared to placebo in hospitalised COVID-19 patients who need oxygen support with symptoms onset 9 days or less. Funding: Ministério da Ciência, Tecnologia e Inovação (MCTI) - Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPQ); Cia Latino-Americana de Medicamentos (Clamed); Cia Industrial H. Carlos Schneider (Ciser); Hospital Research Foundation Incorporation, Australia, HCor São Paulo; Blanver Farmoquímica; Instituto de Tecnologia em Fármacos (Farmanguinhos) da Fundação Oswaldo Cruz (Fiocruz); Coordenação Geral de Planejamento Estratégico (Cogeplan)/Fiocruz; and Fundação de apoio a Fiocruz (Fiotec, VPGDI-054-FIO-20-2-13).

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