216
Participants
Start Date
April 30, 2007
Primary Completion Date
September 30, 2007
Study Completion Date
September 30, 2007
AVX502
1 dose at 2e8 IU given at t=0 via IM route
AVX502
1 dose at 2e7 IU given at T=0 via the IM route
AVX502
1 dose at 2e7 IU given at t=0 via the SC route
AVX502
1 dose at 2e8 IU given at T=0 via the SC route
AVX502
2 doses at 2e7 IU given at T=0 and 8 weeks via the IM route
AVX502
2 doses at 2e8 IU given at T=0 and 8 weeks via the IM route
AVX502
2 doses of 2e7 IU given at t=0 and 8 weeks via the SC route
AVX502
2 doses at 2e8 IU given at T=0 and 8 weeks via the SC route
Placebo
1 dose of placebo given at T=0 via the IM route
Placebo
1 dose of placebo given at T=0 via the SC route
Placebo
2 doses of placebo given at T=0 and 8 weeks via the IM route
Placebo
2 doses of placebo given at T=0 and 8 weeks via the SC route
Johnson County Clin-Trials, Lenexa
Lead Sponsor
AlphaVax, Inc.
INDUSTRY