Safety and Pharmacokinetics of Repeat Dosing of Long-Acting SARS-CoV-2 Antibodies Tixagevimab/Cilgavimab (AZD7442): Results from the PROVENT Sub-study
Dilki Wickramarachchi, Vitalina Dzutseva, Levin Mj, John L. Perez et al.
Journal
Clinical Drug Investigation
Topics
SARS-CoV-2 and COVID-19 Research
article
Safety and Pharmacokinetics of Repeat Dosing of Long-Acting SARS-CoV-2 Antibodies Tixagevimab/Cilgavimab (AZD7442): Results from the PROVENT Sub-study
Dilki Wickramarachchi, Vitalina Dzutseva, Levin Mj, John L. Perez, Odile Launay, Audrey Sharbaugh, Taylor S. Cohen, Bernard Veekmans, Alexandre Kiazand, James G. Sullivan, Mark Vishnepolsky, Katie L. Streicher, Mark T. Esser, Jesse Thissen, Lee-Jah Chang, Stephane De Wit, Meng Li, Lauren Hirao, Rohini Beavon, Huixia Zhang, Seth Seegobin, Tommy Rampling, Priyantha Wijewardane, Andrew Ustianowski, Yousef Fawadleh
article en
Abstract
No abstract available for this paper.
Publication Tag
Clinical Drug InvestigationVol. 46(2)
Institutions
AstraZeneca (United Kingdom) (GB), Université Libre de Bruxelles (BE), University College London Hospitals NHS Foundation Trust (GB), Inserm (FR), Université Paris Cité (FR), North Manchester General Hospital (GB), Assistance Publique – Hôpitaux de Paris (FR), Baptist Health Foundation (US), AstraZeneca (France) (FR), Birmingham VA Medical Center (US), AstraZeneca (Switzerland) (CH), AstraZeneca (Poland) (PL), Kidney Associates (US), DaVita Clinical Research (United States) (US), AstraZeneca (Canada) (CA), AstraZeneca (United States) (US), Centre Hospitalier Universitaire de Saint-Pierre (BE), University College London (GB), University of Colorado Denver (US)