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Completed Phase 2 Interventional Results available

Study to Evaluate the Safety and Efficacy of High Dose Intravenous Immune Globulin (IVIG) Plus Standard Medical Treatment (SMT) Versus SMT Alone in Participants in Intensive Care Unit (ICU) With Coronavirus Disease (COVID-19)

ClinicalTrials.gov ID: NCT04480424

Public ClinicalTrials.gov record NCT04480424. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 6:18 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, Open-label Parallel Group Pilot Study to Evaluate Safety and Efficacy of High Dose Intravenous Immune Globulin (IVIG) Plus Standard Medical Treatment (SMT) Versus SMT Alone in Subjects With COVID-19 Requiring Admission to the Intensive Care Unit

Study identification

NCT ID
NCT04480424
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Grifols Therapeutics LLC
Industry
Enrollment
100 participants

Conditions and interventions

Conditions

Interventions

  • GAMUNEX-C Biological
  • Standard Medical Treatment Drug

Biological · Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 16, 2020
Primary completion
Aug 24, 2021
Completion
Oct 24, 2021
Last update posted
Oct 6, 2022

2020 – 2021

United States locations

U.S. sites
18
U.S. states
14
U.S. cities
18
Facility City State ZIP Site status
Chandler Regional Medical Center Chandler Arizona 85224
Southern California Research Center Coronado California 92118
University of Illinois at Chicago Chicago Illinois 60612
Via Christi Research Wichita Kansas 67214
University of Louisville Louisville Kentucky 40202
Louisiana State University Health Sciences Center Shreveport Louisiana 71103
McLaren Flint Flint Michigan 48532
McLaren Health Care-Macomb Mount Clemens Michigan 48043
McLaren Health Care Oakland Pontiac Michigan 48342
CHI Health Omaha Nebraska 68124
Columbia University Medical Center New York New York 10032
Wake Forest Baptist Medical Center Winston-Salem North Carolina 27517
Summa Health Akron Ohio 44304
Temple University Hospital Philadelphia Pennsylvania 19140
Allegheny Health Network Research Institute Pittsburgh Pennsylvania 15212
CHRISTUS Health Tyler Texas 75701
MultiCare Deaconess Hospital Spokane Washington 99204
MultiCare Tacoma General Hospital Tacoma Washington 98405

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04480424, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 6, 2022 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04480424 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →