drugset / Trial / NCT04452318

COVID-19 Study Assessing the Efficacy and Safety of Anti-Spike SARS CoV-2 Monoclonal Antibodies for Prevention of SARS CoV-2 Infection Asymptomatic in Healthy Adults and Adolescents Who Are Household Contacts to an Individual With a Positive SARS-CoV-2 RT-PCR Assay

NCT04452318 ↗

Phase 3 Completed 3303 enrolled Regeneron Pharmaceuticals
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Primary Objectives: Cohort A: • To evaluate the efficacy of REGN10933+REGN10987 compared to placebo in preventing symptomatic SARS-CoV-2 infection (broad-term) confirmed by RT-qPCR Cohort A and Cohort A1: • To evaluate the safety and tolerability of REGN10933+REGN10987 following subcutaneous (SC) administration compared to placebo Cohort B • To evaluate the efficacy of REGN10933+REGN10987 compared to placebo in preventing COVID-19 symptoms (broad-term) Cohort B and Cohort B1 • To evaluate the safety and tolerability of REGN10933+REGN10987 following SC administration compared to placebo

Timeline

Start
2020-07-13
Primary completion
2021-10-04
Completion
2021-10-04

Outcome

Met primary endpoint

registry analysis (superiority test); Cohort A: Placebo of R10933 + R10987 vs Cohort A: R10933 + R10987; p < 0.0001; Odds Ratio (OR) 0.17 (95% CI 0.090 to 0.332); NCT04452318 ↗

registry analysis (superiority test); Cohort B: Placebo of R10933 + R10987 vs Cohort B: R10933 + R10987; p = 0.0380; Odds Ratio (OR) 0.54 (95% CI 0.298 to 0.966); NCT04452318 ↗

release “to prevent COVID-19 infection among household contacts of SARS-CoV-2 infected individuals. The trial met its primary endpoint” regeneron.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject casirivimab Monoclonal antibody 600 mg Subcutaneous
Subject imdevimab Monoclonal antibody 600 mg Subcutaneous

Indications

No indication recorded.