Last update 01 Dec 2025

IVIG-PEG(Grifols Therapeutics)

Overview

Basic Info

Drug Type
Immunoglobulin
Synonyms-
Target-
Action
stimulants
Mechanism
Immunostimulants
Therapeutic Areas
Immune System DiseasesCongenital DisordersHemic and Lymphatic Diseases+ [1]
Active Indication-
Inactive Indication
Hyper-IgM Immunodeficiency Syndrome
Originator Organization
Grifols Therapeutics, Inc.
Active Organization-
Inactive Organization
Grifols Therapeutics, Inc.
License Organization-
Drug Highest PhasePendingPhase 3
First Approval Date-
Regulation-
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Related

1
Clinical Trials associated with IVIG-PEG(Grifols Therapeutics)
NCT04561115
/ CompletedPhase 3
A Phase 3, Multicenter, Open-label, Single-sequence, Cross-over, Bioequivalence Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of IVIG-PEG Compared to Gamunex-C in Subjects With Primary Humoral Immunodeficiency
100 Clinical Results associated with IVIG-PEG(Grifols Therapeutics)
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100 Translational Medicine associated with IVIG-PEG(Grifols Therapeutics)
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100 Patents (Medical) associated with IVIG-PEG(Grifols Therapeutics)
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100 Deals associated with IVIG-PEG(Grifols Therapeutics)
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Hyper-IgM Immunodeficiency SyndromePhase 3
United States
Grifols Therapeutics, Inc.
02 Sep 2020
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date
NCT04561115 (CTgov)
Phase 3
Primary Immunodeficiency Diseases | Hyper-IgM Immunodeficiency Syndrome
33
(Gamunex-C)
omyzmiywqv(ixmeazvzuu) = rqvcbjecsq sfazzgsyng (thtnmgmkcq, 32848.46)
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-
05 Jun 2023
(IVIG-PEG)
omyzmiywqv(ixmeazvzuu) = hyyvdtxiwq sfazzgsyng (thtnmgmkcq, 36894.29)
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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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