Trial to Evaluate Safety and Immunogenicity of an Ebola Zaire Vaccine in Healthy Adults

PHASE1CompletedINTERVENTIONAL
Enrollment

38

Participants

Timeline

Start Date

December 22, 2015

Primary Completion Date

September 15, 2016

Study Completion Date

September 15, 2016

Conditions
Ebola Virus Disease
Interventions
BIOLOGICAL

Ebola Vaccine - low dose

2 x 0.5ml vaccine will be given as intramuscular injections on each of day 1 and day 28

BIOLOGICAL

Ebola Vaccine - mid dose

2 x 0.5ml vaccine will be given as intramuscular injections on each of day 1 and day 28

BIOLOGICAL

Ebola Vaccine - high dose

2 x 1.0ml vaccine will be given as intramuscular injections on each of day 1 and day 28

BIOLOGICAL

Placebo

2 x 0.5ml or 2 x 1.0ml placebo will be given as intramuscular injections on each of day 1 and day 28 depending on cohort

Trial Locations (1)

32934

Optimal Research, Melbourne

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

Accelovance

INDUSTRY

collaborator

United States Department of Defense

FED

lead

Auro Vaccines LLC

INDUSTRY

NCT02718469 - Trial to Evaluate Safety and Immunogenicity of an Ebola Zaire Vaccine in Healthy Adults | Biotech Hunter | Biotech Hunter