[Articles] Operational effectiveness of tafenoquine and primaquine for the prevention of Plasmodium vivax recurrence in Brazil: a retrospective observational study

Di |2024-03-05T00:30:01+01:00Marzo 5th, 2024|Categorie: Coronavirus Lancet|

In this real-world setting, single-dose tafenoquine was more effective at preventing P vivax recurrence in patients aged at least 16 years who were G6PD normal compared with 7-day primaquine at day 90, while overall efficacy at 180 days was similar. Th...

[Articles] Operational effectiveness of tafenoquine and primaquine for the prevention of Plasmodium vivax recurrence in Brazil: a retrospective observational study

Di |2024-03-05T00:30:01+01:00Marzo 5th, 2024|Categorie: Coronavirus Lancet|

In this real-world setting, single-dose tafenoquine was more effective at preventing P vivax recurrence in patients aged at least 16 years who were G6PD normal compared with 7-day primaquine at day 90, while overall efficacy at 180 days was similar. Th...

[Correspondence] Effectiveness of XBB.1.5 vaccines and antiviral drugs against severe outcomes of omicron infection in the USA

Di |2024-03-05T00:30:01+01:00Marzo 5th, 2024|Categorie: Coronavirus Lancet|

In the fall of 2023, the US Food and Drug Administration (FDA) authorised the use of the updated Moderna (Sept 11), Pfizer-BioNTech (Sept 11), and Novavax (Oct 3) COVID-19 vaccines containing a monovalent component of the XBB.1.5 variant “to provide be...

[Correspondence] Effectiveness of XBB.1.5 vaccines and antiviral drugs against severe outcomes of omicron infection in the USA

Di |2024-03-05T00:30:01+01:00Marzo 5th, 2024|Categorie: Coronavirus Lancet|

In the fall of 2023, the US Food and Drug Administration (FDA) authorised the use of the updated Moderna (Sept 11), Pfizer-BioNTech (Sept 11), and Novavax (Oct 3) COVID-19 vaccines containing a monovalent component of the XBB.1.5 variant “to provide be...

[Corrections] Correction to Lancet Infect Dis 2024; published online Feb 8. https://doi.org/10.1016/S1473-3099(24)00062-8

Di |2024-03-01T00:30:01+01:00Marzo 1st, 2024|Categorie: Coronavirus Lancet|

Wilder-Smith AB, Wilder-Smith A. Determining force of infection for chikungunya to support vaccine policy development. Lancet Infect Dis 2024; published online Feb 8. https://doi.org/10.1016/S1473-3099(24)00062-8—In this Comment, the seventh sentence o...

[Articles] An observer-blind, randomised, placebo-controlled, phase 1, single ascending dose study of dengue monoclonal antibody in healthy adults in Australia

Di |2024-02-24T00:30:01+01:00Febbraio 24th, 2024|Categorie: Coronavirus Lancet|

Dengue monoclonal antibody was safe and well tolerated. It showed a dose-proportionate increase in pharmacokinetic exposure. These data support further evaluation of dengue monoclonal antibody in patients with dengue for safety and efficacy.

[Articles] An observer-blind, randomised, placebo-controlled, phase 1, single ascending dose study of dengue monoclonal antibody in healthy adults in Australia

Di |2024-02-24T00:30:01+01:00Febbraio 24th, 2024|Categorie: Coronavirus Lancet|

Dengue monoclonal antibody was safe and well tolerated. It showed a dose-proportionate increase in pharmacokinetic exposure. These data support further evaluation of dengue monoclonal antibody in patients with dengue for safety and efficacy.

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