Specific IgG Antibody in Patients With Primary Antibody Deficiencies Treated With Subcutaneous Immunoglobulin

NACompletedINTERVENTIONAL
Enrollment

5

Participants

Timeline

Start Date

January 31, 2002

Primary Completion Date

November 30, 2002

Study Completion Date

November 30, 2002

Conditions
Common Variable ImmunodeficiencyAgammaglobulinemia
Interventions
BIOLOGICAL

gammaglobulin

They were administered a polyvalent, pasteurized liquid immune globulin subcutaneously (human 16% Beriglobin ®, Germany) with doses ranging from 57 to 132 mg/kg/week in order to maintain the same dosage they received by intravenous route monthly previous to this protocol. After a wash-out period (15 weeks) of the subcutaneous immunoglobulin administration, blood was collected every 4 weeks immediately before infusions. The infusions were administered using battery-powered ambulatory syringe drivers together with 10 or 20 ml syringe and infusions sets according to a pre-defined protocol (Gardulf et al, 2006).

Trial Locations (1)

Cep 04025-002

Division of Allergy, Clinical Immunology and Rheumatology, Department of Pediatrics, Federal University of São Paulo, São Paulo

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

CSL Behring

INDUSTRY

lead

Federal University of São Paulo

OTHER

NCT00661401 - Specific IgG Antibody in Patients With Primary Antibody Deficiencies Treated With Subcutaneous Immunoglobulin | Biotech Hunter | Biotech Hunter