Last update 29 May 2025

Anti-COVID-19 Immune Globulin (Human)(Grifols Therapeutics)

Overview

Basic Info

Drug Type
Immunoglobulin
Synonyms
C19-IG 20%
Target-
Action-
Mechanism-
Therapeutic Areas
Infectious DiseasesRespiratory DiseasesOther Diseases
Active Indication-
Inactive Indication
COVID-19Severe Acute Respiratory Syndrome
Originator Organization
Grifols Therapeutics LLC
Active Organization-
Inactive Organization
Grifols Therapeutics, Inc.
License Organization-
Drug Highest PhaseDiscontinuedPhase 3
First Approval Date-
Regulation-
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Related

1
Clinical Trials associated with Anti-COVID-19 Immune Globulin (Human)(Grifols Therapeutics)
NCT04847141
/ TerminatedPhase 3
A Multicenter, Randomized, Double-blind, Parallel Group Study to Evaluate the Safety and Efficacy of Anti-COVID-19 Immune Globulin (Human) 20% (C19-IG 20%) Versus Placebo in Asymptomatic Ambulatory Outpatients With Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection
100 Clinical Results associated with Anti-COVID-19 Immune Globulin (Human)(Grifols Therapeutics)
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100 Translational Medicine associated with Anti-COVID-19 Immune Globulin (Human)(Grifols Therapeutics)
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100 Patents (Medical) associated with Anti-COVID-19 Immune Globulin (Human)(Grifols Therapeutics)
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100 Deals associated with Anti-COVID-19 Immune Globulin (Human)(Grifols Therapeutics)
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R&D Status

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IndicationHighest PhaseCountry/LocationOrganizationDate
COVID-19Phase 3
Spain
Grifols Therapeutics, Inc.
28 Apr 2021
Severe Acute Respiratory SyndromePhase 3
Spain
Grifols Therapeutics, Inc.
28 Apr 2021
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date
NCT04847141 (COVID-19, CTgov)
Phase 3
COVID-19 | Severe acute respiratory infection | Severe Acute Respiratory Syndrome
465
0.9% sodium chloride+C19-IG 20%
(C19-IG 20% 1 g)
kivscxrafl = uehujwukof gqyltxladb (zitwosyowt, ggfoeliqsc - gwyyedjkok)
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-
05 Dec 2022
(C19-IG 20% 2 g)
kivscxrafl = ywxbhrpcxe gqyltxladb (zitwosyowt, gtvaqubiaf - umzyactvbm)
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Translational Medicine

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Deal

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Core Patent

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Clinical Trial

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Approval

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Biosimilar

Competitive landscape of biosimilars in different countries/locations. Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3.
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Competitive landscape of biosimilars in different countries/locations. Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3.

Regulation

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