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Safety, Immunogenicity and Efficacy of NVX-CoV2373 in Adolescents in PREVENT-19: A Randomized, Phase 3 Trial
Germán Áñez; Lisa M. Dunkle; Cynthia L. Gay; Karen L. Kotloff; Jeffrey M. Adelglass; Brandon Essink; James D. Campbell; Shane Cloney-Clark; Mingzhu Zhu; Joyce S. Plested; Pavitra Roychoudhury; Alexander L. Greninger; Nita Patel; Alice McGarry; Wayne Woo; Iksung Cho; Gregory M. Glenn; Filip Dubovsky.
Afiliação
  • Germán Áñez; Novavax Inc., Gaithersburg, MD
  • Lisa M. Dunkle; Novavax Inc., Gaithersburg, MD
  • Cynthia L. Gay; University of North Carolina School of Medicine, Chapel Hill, NC
  • Karen L. Kotloff; University of Maryland School of Medicine, Baltimore, MD
  • Jeffrey M. Adelglass; Research Your Health, Plano, TX
  • Brandon Essink; Meridian Clinical Research, Omaha, NE
  • James D. Campbell; University of Maryland School of Medicine, Baltimore, MD
  • Shane Cloney-Clark; Novavax Inc., Gaithersburg, MD
  • Mingzhu Zhu; Novavax Inc., Gaithersburg, MD
  • Joyce S. Plested; Novavax Inc., Gaithersburg, MD
  • Pavitra Roychoudhury; University of Washington Medical Center, Seattle, WA
  • Alexander L. Greninger; University of Washington Medical Center, Seattle, WA
  • Nita Patel; Novavax Inc., Gaithersburg, MD
  • Alice McGarry; Novavax Inc., Gaithersburg, MD
  • Wayne Woo; Novavax Inc., Gaithersburg, MD
  • Iksung Cho; Novavax Inc., Gaithersburg, MD
  • Gregory M. Glenn; Novavax Inc., Gaithersburg, MD
  • Filip Dubovsky; Novavax Inc., Gaithersburg, MD
Preprint em Inglês | medRxiv | ID: ppmedrxiv-22279903
ABSTRACT
BACKGROUNDOver 20% of cases and 0.4% of deaths from Covid-19 occur in children. Following demonstration of safety and efficacy of the adjuvanted, recombinant spike protein vaccine NVX-CoV2373 in adults, the PREVENT-19 trial enrolled adolescents. METHODSSafety, immunogenicity, and efficacy of NVX-CoV2373 were evaluated in adolescents aged 12 to <18 years in an expansion of PREVENT-19, a phase 3, randomized, observer-blinded, placebo-controlled trial in the United States. Participants were randomized 21 to two doses of NVX-CoV2373 or placebo 21 days apart, and followed for a median of 2 months after second vaccination. Primary end points were serologic non-inferiority of neutralizing antibody (NA) responses compared with young adults (18 to <26 years) in PREVENT-19, protective efficacy against laboratory-confirmed Covid-19, and assessment of reactogenicity/safety. RESULTSAmong 2,247 participants randomized between April-June 2021, 1,491 were allocated to NVX-CoV2373 and 756 to placebo. Post-vaccination, the ratio of NA geometric mean titers in adolescents compared to young adults was 1.5 (95% confidence interval [CI] 1.3 to 1.7). Twenty Covid-19 cases (all mild) occurred 6 among NVX-CoV2373 and 14 among placebo recipients (vaccine efficacy [VE] 79.5%, 95% CI, 46.8 to 92.1). All sequenced viral genomes (11/20) were identified as Delta variant (Delta variant VE 82.0% [95% CI 32.4 to 95.2]). Reactogenicity was largely mild-to-moderate, transient, and more frequent in NVX-CoV2373 recipients and after the second dose. Serious adverse events were rare and evenly distributed between treatments. CONCLUSIONSNVX-CoV2373 was safe, immunogenic, and efficacious in the prevention of Covid-19 and those cases caused by the Delta variant in adolescents. (Funded by the Office of the Assistant Secretary for Preparedness and Response, Biomedical Advanced Research and Development Authority and the National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health; PREVENT-19 ClinicalTrials.gov number, NCT04611802).
Licença
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Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Experimental_studies / Estudo prognóstico / Rct Idioma: Inglês Ano de publicação: 2022 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Experimental_studies / Estudo prognóstico / Rct Idioma: Inglês Ano de publicação: 2022 Tipo de documento: Preprint
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