drugset / Trial / NCT04666441

COVID-19 Study Assessing the Virologic Efficacy of REGN10933+REGN10987 Across Different Dose Regimens in Adult Outpatients With SARS-CoV-2 Infection

NCT04666441

Phase 2 Completed 1149 enrolled Regeneron Pharmaceuticals
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of the study is to assess the virologic efficacy of REGN10933+REGN10987 across different intravenous and subcutaneous doses compared to placebo. The secondary objectives of the study are: * To evaluate additional indicators of virologic efficacy of REGN10933+REGN10987 compared to placebo * To evaluate the safety and tolerability of REGN10933+REGN10987 compared to placebo * To assess the concentrations of REGN10933 and REGN10987 in serum over time * To assess the immunogenicity of REGN10933 and REGN10987

Timeline

Start
2020-12-15
Primary completion
2021-03-04
Completion
2021-09-21

Drugs

EvaluationDrugModalityDoseRoute
Subject casirivimab Monoclonal antibody Intravenous
Subject imdevimab Monoclonal antibody Intravenous

Indications