Efficacy and safety of maintenance intravenous immunoglobulin in generalized myasthenia gravis patients with acetylcholine receptor antibodies A multicenter, double-blind, placebo-controlled trial /

Prospective, randomized, controlled trials of intravenous immunoglobulin (IVIG) maintenance therapy in myasthenia gravis (MG) are lacking. In this trial, we evaluated the safety and efficacy of caprylate/chromatography-purified IVIG; (IGIV-C) in patients with generalized MG undergoing standard care....

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Elmentve itt :
Bibliográfiai részletek
Szerzők: Bril Vera
Berkowicz Tomasz
Szczudlik Andrzej
Nicolle Michael W
Bednarik Josef
Hon Petr
Vaitkus Antanas
Vu Tuan
Rozsa Csilla
Magnus Tim
Panczel Gyula
Toomsoo Toomas
Pasnoor Mamatha
Mozaffar Tahseen
Freimer Miriam
Reuner Ulrike
Vécsei László
Souayah Nizar
Levine Todd
Pascuzzi Robert M
Dalakas Marinos C
Rivner Michael
Griffin Rhonda
Coll Montse Querolt
Mondou Elsa
Dokumentumtípus: Cikk
Megjelent: 2025
Sorozat:MUSCLE & NERVE 71 No. 1
Tárgyszavak:
doi:10.1002/mus.28289

mtmt:35508964
Online Access:http://publicatio.bibl.u-szeged.hu/35076
Leíró adatok
Tartalmi kivonat:Prospective, randomized, controlled trials of intravenous immunoglobulin (IVIG) maintenance therapy in myasthenia gravis (MG) are lacking. In this trial, we evaluated the safety and efficacy of caprylate/chromatography-purified IVIG; (IGIV-C) in patients with generalized MG undergoing standard care.Sixty-two patients enrolled in this phase 2, multicenter, international, randomized trial (1:1 IGIV-C [2 g/kg loading dose; 1 g/kg every 3 weeks through week 21] or placebo). Efficacy was assessed by changes in Quantitative MG (QMG) score at week 24 versus baseline (primary endpoint) and percentage of patients with clinical improvement in QMG, MG Composite (MGC), and MG-Activities of Daily Living (MG-ADL) scores (secondary endpoints). Safety assessments reported all adverse events (AEs).The change in QMG at 24 weeks was -5.1 for IGIV-C and -3.1 for placebo (p = .187). Seventy percent of patients in the IGIV-C group had improvement in MG-ADL (≥2-point decrease) versus 40.6% in the placebo group (p = .025). Patients showing clinical improvement in QMG and MGC (≥3-point decrease) were 70.0% for IGIV-C versus 59.4% for placebo (p = .442) and 60.0% for IGIV-C versus 53.1% for placebo (p = .610). IGIV-C was well tolerated; serious AEs were similar between arms. Three of four MG exacerbations requiring hospitalizations occurred in the IGIV-C arm with one death.Several efficacy parameters showed numerical results greater than those seen in the placebo group. This was a small study and may have been underpowered to see significant differences. Additional studies may be warranted to fully determine the efficacy of IVIG maintenance therapy in MG.
Terjedelem/Fizikai jellemzők:43-54
ISSN:0148-639X