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

Outcome

Met primary endpoint

registry Pooled Placebo (IV + SC) vs 300mg IV; p = 0.0004; Difference of LS Means -0.57 (95% CI -0.88 to -0.25) NCT04666441 ↗

paper All casirivimab and imdevimab treatments showed significant virologic reduction through day 7. PMID 35969402 ↗

release “All tested doses met the primary endpoint, rapidly and significantly reducing patients’ viral load (log10 copies/mL) compared to placebo (p<0.001)” roche.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject casirivimab Monoclonal antibody — Intravenous
Subject imdevimab Monoclonal antibody — Intravenous

Indications