Overview

COVID-19 Study of Pharmacokinetics, Safety, Tolerability, and Efficacy of Intravenous Anti-Spike(s) SARS-CoV-2 Monoclonal Antibodies (Casirivimab+Imdevimab) for the Treatment of Pediatric Patients Hospitalized Due to COVID-19

Status:
Not yet recruiting
Trial end date:
2023-06-09
Target enrollment:
Participant gender:
Summary
The primary objectives of the study are: - To characterize the concentrations of casirivimab+imdevimab in serum over time - To evaluate the safety and tolerability of casirivimab+imdevimab The secondary objective of the study is: • To assess the immunogenicity of casirivimab+imdevimab
Phase:
Phase 1
Details
Lead Sponsor:
Regeneron Pharmaceuticals