casirivimab+imdevimab
Sponsors
Regeneron Pharmaceuticals
Conditions
COVID-19Chronic Stable IllnessHealthyImmunocompromised
Phase 1
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
TerminatedNCT05092581
Start: 2021-12-16End: 2022-06-09Updated: 2025-10-14
COVID-19 Study Assessing the Safety and Tolerability of Co-Formulated Anti-Spike (S) SARS-CoV-2 Monoclonal Antibodies (Casirivimab+Imdevimab) in Adult Volunteers
CompletedNCT05181683
Start: 2022-01-07End: 2022-06-03Updated: 2025-10-14
Phase 2
COVID-19 Study to Assess Immunogenicity, Safety, and Tolerability of Moderna mRNA-1273 Vaccine Administered With Casirivimab+Imdevimab in Healthy Adult Volunteers
CompletedNCT04852978
Start: 2021-04-29End: 2022-11-21Updated: 2025-10-17
COVID-19 Administration of Single-Dose Subcutaneous Anti- Spike(s) SARS-CoV-2 Monoclonal Antibodies Casirivimab and Imdevimab in High-Risk Pediatric Participants Under 12 Years of Age
TerminatedNCT04992273
Start: 2021-09-13End: 2022-06-01Updated: 2025-10-17