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Study details
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Outpatient Treatment with Anti-Coronavirus Immunoglobulin Trial

University of Minnesota
NCT IDNCT04910269ClinicalTrials.gov data as of Apr 2026
Phase

Phase 3

Target enrollment

820

Study length

about 5 years

Ages

18+

Locations

22 sites in AZ, CA, CO +10

What this study is about

This trial is testing whether a single infusion of anti-COVID-19 hyperimmune intravenous immunoglobulin (hIVIG) is better than a placebo for adults who have recently been diagnosed with COVID-19 and do not need hospitalization. The goal is to see if hIVIG helps people recover faster and improve their symptoms compared to the placebo.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Placebo
  • 2.Receive Hyperimmune immunoglobulin to SARS-CoV-2 (hIVIG)

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
Randomized & Blinded

You may get a placebo/standard care, and you won't know which.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Secondary: All-cause hospitalization or death through 28 days., Healthcare Utilization at Follow-up

Body systems

Infectious