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. 2016 Feb 24;36:210–219. doi: 10.1007/s10875-016-0243-z

Table 1.

Demographic characteristics of patients from the pooled analysisa

Clinical study (ID) Sandoglobulin® NF liquid (NCT00168012) Privigen® (NCT00168025) Privigen® (NCT00322556)
Total number of patients 42 80 55
Indication, n (%)
 CVID 32 (76.2) 59 (73.8) 44 (80.0)
 XLA 10 (23.8) 21 (26.3) 11 (20.0)
Gender, n (%)
 Female 13 (31.0) 34 (42.5) 29 (52.7)
 Male 29 (69.0) 46 (57.5) 26 (47.3)
Age (years), mean (SD) 32.2 (18.3) 28.2 (19.3) 29.9 (20.8)
BMI (kg/m2), mean (SD) 22.5 (5.1)
(n = 38)
23.5 (6.3)
(n = 80)
24.5 (7.8)
(n = 53)
Duration of PIDb (years),
mean (SD)
10.9 (8.8) 8.6 (7.5) 8.12 (6.8)
IgG trough level (g/L),
mean (SD)
9.95 (2.69)
(n = 41)
9.40 (2.75)
(n = 79)
9.72 (2.23)
(n = 54)
Median weekly dose (mg/kg) 125.5 117.8 128.2

BMI body mass index, CVID common variable immunodeficiency, PID primary immunodeficiency, SD standard deviation, XLA X-linked agammaglobulinemia

aData for well-being are available only for a subset of patients

bPrior to study entry