Table 1.
Cohort | Group | Study Product | Number |
---|---|---|---|
1* | A | 10 μg Sm-TSP-2/Alhydrogel® | 10 |
B | 10 μg Sm-TSP-2/Alhydrogel®/GLA-AF | 10 | |
C | Placebo† | 4 | |
2* | D | 30 μg Sm-TSP-2/Alhydrogel® | 10 |
E | 30 μg Sm-TSP-2/Alhydrogel®/GLA-AF | 10 | |
F | Placebo† | 4 | |
3 | G | 100 μg Sm-TSP-2/Alhydrogel® | 10 |
H | 100 μg Sm-TSP-2/Alhydrogel®/GLA-AF | 10 | |
I | Placebo† | 4 | |
Total | 72 |
Saline for injection.
Dose escalation decisions were made after the last subject in the cohort completed the 7 day post dose 1 visit.