Literature DB >> 21257320

Local tolerance and stability up to 24 months of a new 20% proline-stabilized polyclonal immunoglobulin for subcutaneous administration.

Werner Maeder1, Patricia Lieby, Andrea Sebald, Martin Spycher, Renzo Pedrussio, Reinhard Bolli.   

Abstract

Subcutaneous administration of human IgG is an alternative to intravenous replacement therapy that is associated with more stable serum IgG levels and fewer systemic adverse events. Highly concentrated IgG solutions are most convenient to minimize infusion volume, but their preparation and stability presents substantial technical difficulties. We report on the stability and local tolerance of IgPro20, an l-proline-stabilized, 20% polyvalent human IgG developed for subcutaneous administration. Stability was tested according to ICH guidelines. Local tolerance and vasoactivity were examined in rabbit and rat models, respectively. The presence of l-proline in IgPro20 reduced viscosity and addition of Polysorbate 80 and inert gassing improved the appearance of the solution. After storage at 25 °C for 24 months, monomer + dimer content, aggregates, and fragments were within specification (≥ 90.0%, ≤ 4.0%, and ≤ 10.0%, respectively), and Fc function and antibody activities were maintained. In rats, intravenous injection of IgPro20 produced mild and transient hypotension comparable to that seen with intravenous IgG products. Local tolerance of IgPro20 in rabbits was comparable to that of a marketed subcutaneous IgG, Beriglobin P. Functionality and quality of IgPro20 are maintained during storage at 25 °C for at least 24 months. The product is well tolerated as assessed in animal models.
Copyright © 2010 The International Association for Biologicals. Published by Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 21257320     DOI: 10.1016/j.biologicals.2010.11.004

Source DB:  PubMed          Journal:  Biologicals        ISSN: 1045-1056            Impact factor:   1.856


  5 in total

1.  Efficacy and tolerability of 16% subcutaneous immunoglobulin compared with 20% subcutaneous immunoglobulin in primary antibody deficiency.

Authors:  H B Niebur; C M Duff; G F Shear; D Nguyen; T K Alberdi; M J Dorsey; J W Sleasman
Journal:  Clin Exp Immunol       Date:  2015-07-07       Impact factor: 4.330

Review 2.  Immune globulin subcutaneous (human) 20%: in primary immunodeficiency disorders.

Authors:  Paul L McCormack
Journal:  Drugs       Date:  2012-05-28       Impact factor: 9.546

3.  Efficacy and safety of hizentra®, a new 20% immunoglobulin preparation for subcutaneous administration, in pediatric patients with primary immunodeficiency.

Authors:  Michael Borte; Malgorzata Pac; Margit Serban; Teresa Gonzalez-Quevedo; Bodo Grimbacher; Stephen Jolles; Othmar Zenker; Jutta Neufang-Hueber; Bernd Belohradsky
Journal:  J Clin Immunol       Date:  2011-06-15       Impact factor: 8.317

4.  Enhancing Patient Flexibility of Subcutaneous Immunoglobulin G Dosing: Pharmacokinetic Outcomes of Various Maintenance and Loading Regimens in the Treatment of Primary Immunodeficiency.

Authors:  Jagdev Sidhu; Mikhail Rojavin; Marc Pfister; Jonathan Edelman
Journal:  Biol Ther       Date:  2014-08-14

5.  Nano Differential Scanning Fluorimetry-Based Thermal Stability Screening and Optimal Buffer Selection for Immunoglobulin G.

Authors:  Soo Hyun Kim; Han Ju Yoo; Eun Ji Park; Dong Hee Na
Journal:  Pharmaceuticals (Basel)       Date:  2021-12-25
  5 in total

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