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. Author manuscript; available in PMC: 2022 Apr 22.
Published in final edited form as: Vaccine. 2015 Apr 5;33(21):2470–2476. doi: 10.1016/j.vaccine.2015.03.071

Table 1.

Demographics of subjects participating in four studies1 who received anthrax vaccine adsorbed (AVA) subcutaneously at 0, 2 and 4 weeks2.

Study & group Number of subjects Number (%) females Number (%) Caucasian Number (%) African-American Number (%) other race
Subjects aged 18 to 20 years
AVA000 14 6 11 3 0
AVA005 26 9 21 1 4
AVA006 17 8 16 1 0
AVA009 17 7 10 7 0
Total 74 30 (40.5)2 58 (78.4)2 12 (16.2)2 4 (5.4)2
Subjects aged 21 to 29 years
AVA000 63 31 49 8 6
AVA005 56 24 48 4 4
AVA006 78 41 68 7 3
AVA009 46 24 26 18 2
Total 243 120 (49.4) 191 (78.6) 37 (15.2) 15 (6.2)
1

AVA000 is a Center for Disease Control and Prevention (CDC) study (Ref. [27]) and AVA005, AVA006, and AVA009 (Refs. [2830]) are Biomedical Advanced Research and Development Authority (BARDA) funded studies.

2

P-value assessed as not statistically significant by Fisher’s exact test comparing the 18 to 20 and 21 to 29 year old age groups.