Most immunodeficiencies are related to severe immunoglobulin deficiencies which require lifelong replacement therapy with immunoglobulin G (IgG) to reduce the incidence and severity of infections. IgG can be administered intravenously (IGIV) every 21 or 28 days or subcutaneously every week or every other week (IGSC) for subjects who do not tolerate IV infusions or have difficulties with venous access. No head-to-head data are available to directly compare HyQvia with conventional SCIG. However, SCIG is indicated for administration frequencies from daily up to every other week dosing while HyQvia is indicated for infusion frequencies every 2-4 weeks. This study is designed to assess the IgG trough level after switching from standard SCIG to every other week HyQvia and HyQvia every 3-4 weeks
Open-label, one arm study conducted in France in subjects with PI to IgG trough level at steady state after standard SCIG dosing and after HyQvia administered every other week and every 3-4 weeks at equivalent dose. The study will have three periods: * The first period is a one-week ramp-up period. The first administration of HyQvia will be with a one-week dose as specified in the summary of product characteristics of HyQvia. * During the first three-month follow-up period, HyQvia will be administered, every other week at a dose equivalent to the dose administered with the previous treatment (standard SCIG). * At the end of this first follow-up period, the dose of HyQvia will be increased for the next infusion to reach a 3-week equivalent dose. If it this volume is well tolerated, the following dosing will be a 4-week equivalent dose. HyQvia will then be administered every 3 or 4 weeks for three months.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
22
Sub Cutaneous IgHy10 administration
CHRU, Hôpital Claude Huriez
Lille, France
Hôpital de la Conception
Marseille, France
CHU de Nantes - Hôtel Dieu
Nantes, France
Hôpital St Louis
Paris, France
Hôpital Necker
Paris, France
Hôpital Haut Lévèque
Pessac, France
CHU de Strasbourg
Strasbourg, France
The primary endpoint is the change in IgG trough level at 3 months (visit 3) as compared to baseline (visit 1).
Time frame: Every 2 weeks during the baseline (visit 1) and the 3 months (visit3)
The change in IgG trough level at 6 months (visit 4) as compared to baseline (visit 1) and 3 months (visit 3).
Time frame: Every 3 weeks after the 3 months (visit 3) as 6 months ( visit 4)
Number of adverse reactions
Time frame: 6 months
Incidence rate of adverse reactions
Time frame: 6 months
Number of infection
Time frame: 6 months
The Short Form (36) Health Survey
standardized test for measuring the quality of life
Time frame: at 6 months
Treatment Satisfaction Questionnaire for Medication (TSQM-9).
Time frame: at 6 months
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