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. Author manuscript; available in PMC: 2014 Jun 24.
Published in final edited form as: Vaccine. 2013 May 9;31(29):3025–3033. doi: 10.1016/j.vaccine.2013.04.050

Table 2.

Demographic Data by Study Group

Category Sub-category Group 0+7 IMVAMUNE1 Days 0, 7 (N=61) Group 0+28 IMVAMUNE1 Days 0, 28 (N=67) Group 0 IMVAMUNE1 Day 0 (N=63) Placebo2 (N=17) All Groups (N=208)
GENDER Male 36 (59.0%) 31 (46.3%) 31 (49.2%) 9 (52.9%) 107 (51.4%)
Female 25 (41.0%) 36 (53.7%) 32 (50.8%) 8 (47.1%) 101 (48.6%)
RACE White 52 (85.2%) 57 (85.1%) 54 (85.7%) 15 (88.2%) 178 (85.6%)
Black 5 (8.2%) 3 (4.5%) 6 (9.5%) 1 (5.9%) 15 (7.2%)
Asian 0 2 (3.0%) 2 (3.2%) 1 (5.9%) 5 (2.4%)
Multiracial 4 (6.6%) 3 (4.5%) 1 (1.6%) 0 8 (3.8%)
Not Reported 0 2 (3.0%) 0 0 2 (1.0%)
ETHNICITY Non-Hispanic/Latino 59 (96.7%) 64 (95.5%) 60 (95.2%) 16 (94.1%) 199 (95.7%)
Hispanic/Latino 2 (3.3%) 3 (4.5%) 3 (4.8%) 1 (5.9%) 9 (4.3%)
AGE Mean (S.D.) 24.7 (4.6) 25.0 (3.9) 24.3 (3.9) 25.4 (4.5) 24.7 (4.2)
Median 23 24 24 25 24
Range [Min., Max.] [18, 35] [18, 35] [18, 35] [19, 35] [18, 35]
1

Vaccine: IMVAMUNE 0.5 mL of 1× 108 cfu/mL administered subcutaneously on Days 0 and 7 (Group 0+ 7), Days 0 and 28 (Group 0+28) and Day 0 (Group 0).

2

Placebo: Saline 0.5 mL administered subcutaneously on Days 0 and 7 (Group 0+ 7, n= 6), Days 0 and 28 (Group 0+28, n=5) and Day 0 (Group 0, n=7).