MVA Post-Event: Administration Timing and Boost Study

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

226

Participants

Timeline

Start Date

April 16, 2007

Primary Completion Date

April 21, 2009

Study Completion Date

April 21, 2009

Conditions
Smallpox
Interventions
BIOLOGICAL

Live vaccinia virus vaccine

Dryvax® Vaccinia Vaccine (\~10\^5 \[plaque forming units (pfu)/dose\] given via scarification, titer 10\^8 pfu per mL after reconstitution).

BIOLOGICAL

MVA Smallpox Vaccine

IMVAMUNE® Vaccinia Vaccine delivered by subcutaneous (SC) route at titer 1X10\^8 Tissue Culture Infections Dose50 per 0.5 mL dose.

OTHER

Placebo

0.9 percent (weight/volume) sodium chloride injection, United States Pharmacopeia \[Sterile Saline Placebo (SSP)\].

OTHER

Placebo

Physiologic normal saline for injection.

Trial Locations (7)

52242-2600

University of Iowa - Vaccine Research and Education Unit, Iowa City

21201-1509

University of Maryland, School of Medicine, Center for Vaccine Development and Global Health, Baltimore

63104-1015

Saint Louis University Center for Vaccine Development, St Louis

14642-0001

University of Rochester Medical Center - Strong Memorial Hospital - Infectious Diseases, Rochester

27704-2120

Duke Translational Medicine Institute - Clinical Vaccine Unit, Durham

44106-3808

Case Western Reserve University - John T. Carey Special Immunology Unit, Cleveland

77555-5302

University of Texas Medical Branch - Pediatrics - Infectious Diseases and Immunology - Galveston, Galveston

All Listed Sponsors
lead

National Institute of Allergy and Infectious Diseases (NIAID)

NIH

NCT00437021 - MVA Post-Event: Administration Timing and Boost Study | Biotech Hunter | Biotech Hunter