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VPM1002 as Prophylaxis Against Severe Respiratory Tract Infections Including Coronavirus Disease 2019 in the Elderly: A Phase 3 Randomized, Double-Blind, Placebo-Controlled, Multicenter Clinical Study.
Blossey, Alexandra M; Brückner, Sina; May, Marcus; Parzmair, Gerald P; Sharma, Hitt; Shaligram, Umesh; Grode, Leander; Kaufmann, Stefan H E; Netea, Mihai G; Schindler, Christoph.
Afiliación
  • Blossey AM; Vakzine Projekt Management GmbH, Hannover, Germany.
  • Brückner S; Vakzine Projekt Management GmbH, Hannover, Germany.
  • May M; Vakzine Projekt Management GmbH, Hannover, Germany.
  • Parzmair GP; Vakzine Projekt Management GmbH, Hannover, Germany.
  • Sharma H; Serum Institute of India Private Limited, Pune, India.
  • Shaligram U; Serum Institute of India Private Limited, Pune, India.
  • Grode L; Vakzine Projekt Management GmbH, Hannover, Germany.
  • Kaufmann SHE; Max Planck Institute for Infection Biology, Berlin, Germany.
  • Netea MG; Hagler Institute for Advanced Study, Texas A&M University, College Station, Texas, USA.
  • Schindler C; Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.
Clin Infect Dis ; 76(7): 1304-1310, 2023 04 03.
Article en En | MEDLINE | ID: mdl-36358012
BACKGROUND: Bacille Calmette-Guérin (BCG) vaccination can potentially reduce the rate of respiratory infections in vulnerable populations. This study evaluates the safety and efficacy of VPM1002 (a genetically modified BCG) as prophylaxis against severe respiratory tract infections including coronavirus disease 2019 (COVID-19) in an elderly population. METHODS: In this phase 3, randomized, double-blind, placebo-controlled, multicenter clinical trial, healthy elderly volunteers (N = 2064) were enrolled, randomized (1:1) to receive either VPM1002 or placebo, and followed up remotely for 240 days. The primary outcome was the mean number of days with severe respiratory infections at hospital and/or at home. Secondary endpoints included the incidence of self-reported fever, number of hospital and intensive care unit (ICU) admissions, and number of adverse events. RESULTS: A total of 31 participants in the VPM1002 group reported at least 1 day with severe respiratory disease and a mean number of days with severe respiratory disease of 9.39 ± 9.28 while in the placebo group; 38 participants reported a mean of 14.29 ± 16.25 days with severe respiratory disease. The incidence of self-reported fever was lower in the VPM1002 group (odds ratio, 0.46 [95% confidence interval, .28-.74]; P = .001), and consistent trends to fewer hospitalization and ICU admissions due to COVID-19 were observed after VPM1002 vaccination. Local reactions typical for BCG were observed in the VPM1002-vaccinated group, which were mostly of mild intensity. CONCLUSIONS: Vaccination with VPM1002 is well tolerated and seems to have a prophylactic effect against severe respiratory disease in the elderly. CLINICAL TRIALS REGISTRATION: NCT04435379.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Vacuna BCG / COVID-19 Tipo de estudio: Clinical_trials Límite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Infect Dis Asunto de la revista: DOENCAS TRANSMISSIVEIS Año: 2023 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Vacuna BCG / COVID-19 Tipo de estudio: Clinical_trials Límite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Infect Dis Asunto de la revista: DOENCAS TRANSMISSIVEIS Año: 2023 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Estados Unidos