Safety, Immunogenicity and Efficacy Against of a Combined Malaria Vaccine in Healthy Malaria-naïve Adults

PHASE2CompletedINTERVENTIONAL
Enrollment

67

Participants

Timeline

Start Date

August 10, 2011

Primary Completion Date

February 27, 2012

Study Completion Date

July 3, 2012

Conditions
Malaria
Interventions
BIOLOGICAL

Crucell's replication deficient adenovirus type 35 circumsporozoite malaria vaccine (Ad35.CS.01)

One dose will be administered intramuscularly at Study Day 0.

BIOLOGICAL

GSK Biologicals' malaria vaccine 257049 (2 doses)

Two doses will be administered intramuscularly at monthly intervals

BIOLOGICAL

GSK Biologicals' malaria vaccine 257049 (3 doses)

Three doses will be administered intramuscularly at monthly intervals

OTHER

Sporozoite challenge

Subjects were challenged with sporozoite-infected mosquitoes to determine whether immune protective response had been induced by vaccination.

Trial Locations (1)

20910

GSK Investigational Site, Silver Spring

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

The PATH Malaria Vaccine Initiative (MVI)

OTHER

collaborator

Crucell Holland BV

INDUSTRY

lead

GlaxoSmithKline

INDUSTRY

NCT01366534 - Safety, Immunogenicity and Efficacy Against of a Combined Malaria Vaccine in Healthy Malaria-naïve Adults | Biotech Hunter | Biotech Hunter