COVIDIG (COVID-19 Hyper-ImmunoGlobulin)

NCT04555148 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 63

Last updated 2021-08-24

No results posted yet for this study

Summary

The objective of this study is to evaluate the efficacy and safety of 5131A for hospitalized patients of COVID-19.

Conditions

  • Covid19

Interventions

BIOLOGICAL

GC5131

COVID19 Hyper-Immunoglobulin

OTHER

Placebo

Placebo

Sponsors & Collaborators

  • Green Cross Corporation

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
19 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-09-19
Primary Completion
2021-01-22
Completion
2021-04-23

Countries

  • South Korea

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04555148 on ClinicalTrials.gov