Safety and Immunogenicity Study of Rift Valley Fever Vaccine

PHASE2CompletedINTERVENTIONAL
Enrollment

278

Participants

Timeline

Start Date

June 30, 2004

Primary Completion Date

May 31, 2010

Study Completion Date

May 31, 2010

Conditions
Rift Valley Fever
Interventions
BIOLOGICAL

TSI-GSD 200 RVF Vaccine

Part A: Inactivated, Dried (TSI-GSD 200) RVF vaccine will be given as three 1.0-ml subcutaneous primary series injections, with doses on day 0, once on days 7-14, once on days 28-42 (the third dose will be given at least 21 days after the second dose).Part B: Subcutaneous 1.0-ml booster doses (maximum of four boosters over 12 months) will be given if the volunteer fails to respond to the primary series with a PRNT80 ≥ 1:40 or annually if titer wanes to \< 1:40.

Trial Locations (1)

21702

U.S. Army Medical Research Institute of Infectious Diseases, Fort Deterick

All Listed Sponsors
lead

U.S. Army Medical Research and Development Command

FED

NCT00584194 - Safety and Immunogenicity Study of Rift Valley Fever Vaccine | Biotech Hunter | Biotech Hunter