Safety and Immunogenicity of a Human Hookworm Candidate Vaccine With Different Doses of a Novel Adjuvant

PHASE1CompletedINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

May 31, 2012

Primary Completion Date

January 31, 2015

Study Completion Date

June 30, 2015

Conditions
Hookworm InfectionHookworm Disease
Interventions
BIOLOGICAL

10 μg Na-GST-1/Alhydrogel

3 doses 10 μg Na-GST-1/Alhydrogel administered at 56 day intervals

BIOLOGICAL

30 μg Na-GST-1/Alhydrogel

3 doses 30 μg Na-GST-1/Alhydrogel administered at 56 day intervals

BIOLOGICAL

100 μg Na-GST-1/Alhydrogel

3 doses 100 μg Na-GST-1/Alhydrogel administered at 56 day intervals

BIOLOGICAL

10 μg Na-GST-1/Alhydrogel/GLA-AF (1 μg)

3 doses 10 μg Na-GST-1/Alhydrogel/GLA-AF (1 μg) administered at 56 day intervals

BIOLOGICAL

30 μg Na-GST-1/Alhydrogel/GLA-AF (1 μg)

3 doses of 30 μg Na-GST-1/Alhydrogel/GLA-AF (1 μg) administered at 56 day intervals

BIOLOGICAL

30 μg Na-GST-1/Alhydrogel/GLA-AF (5 μg)

3 doses 30 μg Na-GST-1/Alhydrogel/GLA-AF (5 μg) administered at 56 day intervals

BIOLOGICAL

100 μg Na-GST-1/Alhydrogel/GLA-AF (5 μg)

3 doses 100 μg Na-GST-1/Alhydrogel/GLA-AF (5 μg) administered at 56 day intervals

Trial Locations (1)

20010

Children's National Medical Center, Washington D.C.

All Listed Sponsors
collaborator

Children's National Research Institute

OTHER

collaborator

George Washington University

OTHER

lead

Baylor College of Medicine

OTHER