Combination Study With MVA BN and Dryvax

PHASE1CompletedINTERVENTIONAL
Enrollment

91

Participants

Timeline

Start Date

May 31, 2004

Primary Completion Date

August 31, 2007

Study Completion Date

August 31, 2007

Conditions
Smallpox
Interventions
BIOLOGICAL

Live vaccinia virus vaccine

Dryvax®: 0.25 mL of vaccine will be administered by the standard route of scarification using a bifurcated needle on day 112 for Groups A, B, C, D and F.

BIOLOGICAL

MVA Smallpox Vaccine

Imvamune/MVA-BN 1x10\^8 will be administered intramuscularly to Group F on day 0 and day 28.

BIOLOGICAL

MVA Smallpox Vaccine

Imvamune/MVA-BN Groups A, B C and E will be administered subcutaneously: 2x10\^7, 5x10\^7, 1x10\^8, 1x10\^8, respectively, on days 0 and day 28.

OTHER

Placebo

Group E will receive sterile saline placebo for injection via scarification on day 112.

OTHER

Placebo

Group D will receive sterile saline placebo for injection subcutaneously on day 0 and day 28.

Trial Locations (1)

63110

Saint Louis University, St Louis

All Listed Sponsors
lead

National Institute of Allergy and Infectious Diseases (NIAID)

NIH

NCT00082446 - Combination Study With MVA BN and Dryvax | Biotech Hunter | Biotech Hunter