
Iranian Journal of Medical Microbiology, Journal Year: 2024, Volume and Issue: 18(5), P. 308 - 318
Published: Nov. 30, 2024
Language: Английский
Iranian Journal of Medical Microbiology, Journal Year: 2024, Volume and Issue: 18(5), P. 308 - 318
Published: Nov. 30, 2024
Language: Английский
Vaccines, Journal Year: 2024, Volume and Issue: 12(10), P. 1180 - 1180
Published: Oct. 17, 2024
COVID-19 vaccines have reduced the negative health and economic impact of pandemic by preventing severe disease, hospitalizations deaths. In new socio-economic normality, vaccination strategy can be universal or high-risk seasonal not seasonal, different used. The achieve greater herd immunity effects is associated with costs than strategy. each country, optimal must decided considering advantages disadvantages assessing costs, cost-effectiveness strategies. should implemented when objective program to greatest benefits from its incremental ratio lower EUR 30,000-50,000 per QALY LYG. use adapted targeting currently circulating variants SARS-CoV-2 necessary avoid immune escape emerging variants.
Language: Английский
Citations
0Human Vaccines & Immunotherapeutics, Journal Year: 2024, Volume and Issue: 20(1)
Published: Nov. 29, 2024
The objective of the study was to assess safety, tolerability, and potential efficacy intranasally administered AD17002, a detoxified form Escherichia coli heat-labile enterotoxin, in treating individuals with mild-to-moderate coronavirus disease 2019 (COVID-19). In this randomized, double-blinded, placebo-controlled phase 2a study, total 30 adults aged 20–70 years COVID-19 were recruited from three medical centers Taiwan 2022–2023. trial comprised two cohorts, participants randomly assigned receive intranasal administrations either doses AD17002 immunomodulator or placebo formulation buffer. Outcome analyses conducted on intention-to-treat set, safety set that included all randomized exposed AD17002. proportion cycle threshold (Ct) ≥30 time recovery key symptoms assessed. An exploratory analyze integrity viral genome after treatment. Administering 20 μg times, at 1-week 1-day intervals, proved be safe well tolerated subjects COVID-19. demonstrated rapid positive outcome reducing load patients receiving Impact treatment further supported by analysis following enhancement clinical within 5 days symptom onset observed but did not achieve statistical significance. According results, administration safe, well-tolerated, potentially effective for
Language: Английский
Citations
0Published: Nov. 29, 2024
Language: Английский
Citations
0Iranian Journal of Medical Microbiology, Journal Year: 2024, Volume and Issue: 18(5), P. 308 - 318
Published: Nov. 30, 2024
Language: Английский
Citations
0