Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/222105
Title: The Results of ADVANCE-CIDP IVIG Trial: Intravenous Immunoglobulin 10% Therapy With GAMMAGARD LIQUID Kiovig for Treatment of Relapse in Chronic Inflammatory Demyelinating Polyradiculoneuropathy
Author: Pasnoor, Mamatha
Anderson Smits, Colin
Levine, Todd
Bril, Vera
Marcos Solano, Juan
Rejdak, Konrad
Gamez, Josep
Chroni, Elisabeth
Casasnovas, Carlos
Marchioni, Enrico
Siciliano, Gabriele
Cocito, Dario
Sivakumar, K.
Rivero, Alberto
Duff, Kim
Greco, Erin
Corbo, Massimo
Hasan, Shabbir
Dori, Amir
Schmidt, Jens
Wood, Jamie
Li, Zhaoyang
Ay, Hakan
Keywords: Malalties autoimmunitàries
Immunoglobulina G
Immunoglobulines
Malalties del sistema nerviós
Autoimmune diseases
Immunoglobulin G
Immunoglobulins
Nervous system Diseases
Issue Date: 1-Apr-2025
Publisher: Wiley
Abstract: Background ADVANCE-CIDP IVIG evaluated the efficacy and safety of immune globulin infusion (human) 10% solution (IVIG 10%; GAMMAGARD LIQUID, also known as Kiovig) in chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) as a rescue treatment for patients relapsing during the ADVANCE-CIDP 1 trial.MethodsOpen-label ADVANCE-CIDP IVIG included adult patients with confirmed CIDP relapse (>= 1-point increase in adjusted Inflammatory Neuropathy Cause and Treatment [INCAT] disability scores from pre-treatment baseline) during ADVANCE-CIDP 1, which assessed the efficacy and safety of hyaluronidase-facilitated subcutaneous immunoglobulin (fSCIG) 10%. Patients received an induction IVIG 10% dose (2 g/kg) followed by maintenance infusions at the same monthly equivalent dose of pre-randomization IVIG, 3-weekly for 6 months. The primary outcome was the responder rate (>= 1-point decrease in adjusted INCAT scores at treatment cessation vs. pre-IVIG 10% baseline, in patients receiving placebo in ADVANCE-CIDP 1). Other outcomes included the responder rate across all patients relapsing on fSCIG 10% or placebo in ADVANCE-CIDP 1, time to functional improvement (>= 1-point decrease in adjusted INCAT score), and change in adjusted INCAT scores and Rasch-built Overall Disability Scale (R-ODS) centile scores from pre-IVIG 10% baseline.ResultsOverall, 20 patients received IVIG 10% (n = 4 [fSCIG 10%-relapse group]; n = 16 [placebo-relapse group]). Responder rate (95% confidence interval) was 100.0% (80.6%-100.0%) in the placebo-relapse group and 95.0% (76.4%-99.1%) in the overall-relapse population. Across all patients, median time to functional improvement was 25 days. At treatment cessation, mean changes from pre-IVIG 10% baseline in adjusted INCAT and R-ODS centile scores were -1.9 and 12.9, respectively.ConclusionsIVIG 10% effectively treated CIDP relapse and improved functional abilities.
Note: Reproducció del document publicat a: https://doi.org/10.1111/ene.70110
It is part of: European Journal of Neurology, 2025, vol. 32, num. 4, p. e70110
URI: https://hdl.handle.net/2445/222105
Related resource: https://doi.org/10.1111/ene.70110
ISSN: 1468-1331
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))



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