CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 3,303 enrolled
Drug / intervention
REGN10933 + REGN10987 +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04452318
NCT04452318Phase 3Completed

A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study Assessing the Efficacy and Safety of Anti-Spike SARS-CoV-2 Monoclonal Antibodies in Preventing SARS-CoV-2 Infection in Household Contacts of Individuals Infected With SARS-CoV-2

Regeneron Pharmaceuticals·interventional·Posted Jun 30, 2020·Updated May 15, 2023

In Brief

A Phase 3 clinical trial evaluating REGN10933 + REGN10987 and Placebo for Healthy Participants. Completed, enrolled 3,303 participants across 134 sites in 3 countries.

Detailed 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

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesMoldova, Romania, United States
Collaborators--

Timeline

Phase 3CompletedFinished
202120222023202420252026
First PostedJun 30, 2020
Enrollment StartJul 13, 2020
Primary CompletionOct 4, 2021
TodayJul 2, 2026
Enrollment to primary: 1.2 yearsPosted 6.0 years ago

Interventions

REGN10933 + REGN10987drug

Subcutaneous (SC) or Intramuscular (IM) injections

Placebodrug

SC or IM injections