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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 trial.
Maia, Israel S; Marcadenti, Aline; Veiga, Viviane C; Miranda, Tamiris A; Gomes, Samara P C; Carollo, Mariana B S; Negrelli, Karina L; Gomes, Jackeline O; Tramujas, Lucas; Abreu-Silva, Erlon O; Westphal, Glauco A; Fernandes, Ruthy P; Horta, Jacques G A; Oliveira, Deborah C; Flato, Uri A P; Paoliello, Ricardo C R; Fernandes, Camilo; Zandonai, Cássio L; Coelho, Juliana C; Barros, Waldemar C; Lemos, Juliana C; Bolan, Renata S; Dutra, Marcela M; Gebara, Otavio C E; Lopes, Ana T A; Alencar Filho, Meton S; Arraes, Jussara A; Hamamoto, Victor A; Hernandes, Mauro E; Golin, Nicole A; Santos, Tiago M; Santos, Renato H N; Damiani, Lucas P; Zampieri, Fernando G; Gesto, João; Machado, Flávia R; Rosa, Régis G; Azevedo, Luciano C P; Avezum, Alvaro; Lopes, Renato D; Souza, Thiago M L; Berwanger, Otávio; Cavalcanti, Alexandre B.
Afiliação
  • Maia IS; HCor Research Institute, São Paulo, SP, Brazil.
  • Marcadenti A; ICU Nereu Ramos, Hospital Nereu Ramos, Florianópolis, SC, Brazil.
  • Veiga VC; Brazilian Intensive Care Research Network, BricNet, São Paulo, Brazil.
  • Miranda TA; Divisão de Anestesiologia, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.
  • Gomes SPC; HCor Research Institute, São Paulo, SP, Brazil.
  • Carollo MBS; Brazilian Intensive Care Research Network, BricNet, São Paulo, Brazil.
  • Negrelli KL; BP ICU - A Beneficência Portuguesa de São Paulo, São Paulo, SP, Brazil.
  • Gomes JO; HCor Research Institute, São Paulo, SP, Brazil.
  • Tramujas L; HCor Research Institute, São Paulo, SP, Brazil.
  • Abreu-Silva EO; HCor Research Institute, São Paulo, SP, Brazil.
  • Westphal GA; HCor Research Institute, São Paulo, SP, Brazil.
  • Fernandes RP; HCor Research Institute, São Paulo, SP, Brazil.
  • Horta JGA; HCor Research Institute, São Paulo, SP, Brazil.
  • Oliveira DC; HCor Research Institute, São Paulo, SP, Brazil.
  • Flato UAP; ICU Centro Hospitalar Unimed, Joinville, SC, Brazil.
  • Paoliello RCR; ICU Centro Hospitalar Unimed, Joinville, SC, Brazil.
  • Fernandes C; Santa Casa de Misericórdia de Ouro Preto, Ouro Preto, MG, Brazil.
  • Zandonai CL; Santa Casa de Misericórdia de Ouro Preto, Ouro Preto, MG, Brazil.
  • Coelho JC; Universidade de Marília, Marília, São Paulo, Brazil.
  • Barros WC; Universidade de Marília, Marília, São Paulo, Brazil.
  • Lemos JC; ICU Nereu Ramos, Hospital Nereu Ramos, Florianópolis, SC, Brazil.
  • Bolan RS; ICU Nereu Ramos, Hospital Nereu Ramos, Florianópolis, SC, Brazil.
  • Dutra MM; BP ICU - A Beneficência Portuguesa de São Paulo, São Paulo, SP, Brazil.
  • Gebara OCE; Unimed Sul Capixaba, Cachoeiro de Itapemirim, ES, Brazil.
  • Lopes ATA; Unimed Sul Capixaba, Cachoeiro de Itapemirim, ES, Brazil.
  • Alencar Filho MS; Research Institute Baía Sul, Hospital Baía Sul, Florianópolis, SC, Brazil.
  • Arraes JA; Research Institute Baía Sul, Hospital Baía Sul, Florianópolis, SC, Brazil.
  • Hamamoto VA; Hospital Santa Paula, São Paulo, SP, Brazil.
  • Hernandes ME; Hospital Santa Paula, São Paulo, SP, Brazil.
  • Golin NA; Hospital Maternidade São Vicente de Paulo, Barbalha, CE, Brazil.
  • Santos TM; Hospital Maternidade São Vicente de Paulo, Barbalha, CE, Brazil.
  • Santos RHN; Research Institute, Hospital Alemão Oswaldo Cruz, São Paulo, SP, Brazil.
  • Damiani LP; International Research Center, Hospital Alemão Oswaldo Cruz, São Paulo, SP, Brazil.
  • Zampieri FG; Santa Casa de Votuporanga, Votuporanga, Brazil.
  • Gesto J; Hospital Tacchini, Bento Gonçalves, Brazil.
  • Machado FR; HCor Research Institute, São Paulo, SP, Brazil.
  • Rosa RG; Insper-Institute of Education and Research, São Paulo, SP, Brazil.
  • Azevedo LCP; HCor Research Institute, São Paulo, SP, Brazil.
  • Avezum A; HCor Research Institute, São Paulo, SP, Brazil.
  • Lopes RD; Academic Research Institute, Hospital Israelita Albert Einstein, São Paulo, SP, Brazil.
  • Souza TML; Brazilian Intensive Care Research Network, BricNet, São Paulo, Brazil.
  • Berwanger O; Academic Research Institute, Hospital Israelita Albert Einstein, São Paulo, SP, Brazil.
  • Cavalcanti AB; Instituto Nacional de Ciência e Tecnologia de Inovação Em Doenças de Populações Negligenciadas, Centro de Desenvolvimento Tecnológico Em Saúde, Fundação Oswaldo Cruz, Rio de Janeiro, RJ, Brazil.
Lancet Reg Health Am ; 20: 100466, 2023 Apr.
Article em En | MEDLINE | ID: mdl-36908503
ABSTRACT

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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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials País/Região como assunto: America do sul / Brasil Idioma: En Revista: Lancet Reg Health Am Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Brasil

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials País/Região como assunto: America do sul / Brasil Idioma: En Revista: Lancet Reg Health Am Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Brasil