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NCT04666441 · ClinicalTrials.gov registry record · Phase 2

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

A Phase 2 study, sponsored by Regeneron Pharmaceuticals.

Completed
Registry status
Phase 2
Development phase
1,149
Enrollment target

NCT04666441 is a Phase 2 study that has completed, run by Regeneron Pharmaceuticals. The registered enrollment target is 1,149 participants.

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The verdict

NCT04666441, a Phase 2 study, has completed, sponsored by Regeneron Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
1,149 participants
Enrollment target

Study 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

Interventions

  • DRUG Placebo
  • DRUG REGN10933+REGN10987 combination therapy

Trial Details

FieldValue
Enrollment Target 1,149 participants
Start Date 2020-12-15
Est. Completion 2021-09-21
Phase Phase 2

Sponsor

Regeneron Pharmaceuticals

280 total trials

What the Registry Record Tells You About NCT04666441

The ClinicalTrials.gov registry entry for NCT04666441 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 1,149 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Regeneron Pharmaceuticals, which has 280 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT04666441 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT04666441 about?

NCT04666441 is a clinical study titled "COVID-19 Study Assessing the Virologic Efficacy of REGN10933+REGN10987 Across Different Dose Regimens in Adult Outpatients With SARS-CoV-2 Infection". 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 compare...

What is the current status of trial NCT04666441?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 1,149 participants. The study started on 2020-12-15. Estimated completion is 2021-09-21.

What interventions are being tested in trial NCT04666441?

The interventions under investigation include: Placebo (DRUG), REGN10933+REGN10987 combination therapy (DRUG).

Who is sponsoring clinical trial NCT04666441?

This trial is sponsored by Regeneron Pharmaceuticals, which has 280 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.