[HTML][HTML] Safety and efficacy of the ChAdOx1 nCoV-19 vaccine (AZD1222) against SARS-CoV-2: an interim analysis of four randomised controlled trials in Brazil, South …

…, M Toshner, DPJ Turner, J Vekemans, TL Villafana… - The Lancet, 2021 - thelancet.com
Background A safe and efficacious vaccine against severe acute respiratory syndrome
coronavirus 2 (SARS-CoV-2), if deployed with high coverage, could contribute to the control of …

[HTML][HTML] Safety and immunogenicity of ChAdOx1 nCoV-19 vaccine administered in a prime-boost regimen in young and old adults (COV002): a single-blind …

…, Y Themistocleous, KM Thomas, TL Villafana… - The Lancet, 2020 - thelancet.com
T-cell responses peaked at day 14 after a single standard dose of ChAdOx1 nCoV-19 (18–55
years: median 1187 spot-forming cells [SFCs] per million peripheral blood mononuclear …

[HTML][HTML] Phase 3 safety and efficacy of AZD1222 (ChAdOx1 nCoV-19) Covid-19 vaccine

…, RP Marshall, MN Pangalos, T Villafana… - … England Journal of …, 2021 - Mass Medical Soc
Background The safety and efficacy of the AZD1222 (ChAdOx1 nCoV-19) vaccine in a large,
diverse population at increased risk for severe acute respiratory syndrome coronavirus 2 (…

[HTML][HTML] Correlates of protection against symptomatic and asymptomatic SARS-CoV-2 infection

…, KM Thomas, J Vekemans, TL Villafana, T Lambe… - Nature medicine, 2021 - nature.com
… The potential role of T cells and interaction between humoral and cellular immunity has
not been evaluated in this study. It is not possible to determine in this study if our results …

[HTML][HTML] Single-dose administration and the influence of the timing of the booster dose on immunogenicity and efficacy of ChAdOx1 nCoV-19 (AZD1222) vaccine: a …

…, DPJ Turner, J Vekemans, TL Villafana, T White… - The Lancet, 2021 - thelancet.com
Background The ChAdOx1 nCoV-19 (AZD1222) vaccine has been approved for emergency
use by the UK regulatory authority, Medicines and Healthcare products Regulatory Agency, …

[HTML][HTML] Efficacy of the ChAdOx1 nCoV-19 Covid-19 vaccine against the B. 1.351 variant

…, NM Durham, EJ Kelly, TL Villafana… - … England Journal of …, 2021 - Mass Medical Soc
Background Assessment of the safety and efficacy of vaccines against the severe acute
respiratory syndrome coronavirus 2 (SARS-CoV-2) in different populations is essential, as is …

[HTML][HTML] Nirsevimab for prevention of RSV in healthy late-preterm and term infants

…, A Leach, MP Griffin, T Villafana - … England Journal of …, 2022 - Mass Medical Soc
Background Respiratory syncytial virus (RSV) is a major cause of lower respiratory tract
infection and hospitalization in infants. Nirsevimab is a monoclonal antibody to the RSV fusion …

Recruitment and retention of pregnant women into clinical research trials: an overview of challenges, facilitators, and best practices

…, JS Sheffield, KM Edwards, T Villafana… - Clinical Infectious …, 2014 - academic.oup.com
Pregnant women are a vulnerable group who are needed in clinical research studies to
advance prevention and treatment options for this population. Yet, pregnant women remain …

[HTML][HTML] Efficacy of ChAdOx1 nCoV-19 (AZD1222) vaccine against SARS-CoV-2 variant of concern 202012/01 (B. 1.1. 7): an exploratory analysis of a randomised …

…, TL Villafana, CJ Williams, AVS Hill, T Lambe… - The Lancet, 2021 - thelancet.com
Background A new variant of SARS-CoV-2, B.1.1.7, emerged as the dominant cause of
COVID-19 disease in the UK from November, 2020. We report a post-hoc analysis of the efficacy …

Nirsevimab for prevention of RSV in term and late-preterm infants

…, M Shroff, T Takas, A Leach, T Villafana - … England Journal of …, 2023 - Mass Medical Soc
Nirsevimab to Prevent RSV Illness in Infants Nirsevimab, a monoclonal antibody targeting
respiratory syncytial virus, protected against RSV-associated hospitalization and severe …