EuroNeut41: Safety & Immunogenicity of Immunisations With HIV Vaccine

PHASE1CompletedINTERVENTIONAL
Enrollment

48

Participants

Timeline

Start Date

January 31, 2012

Primary Completion Date

June 30, 2013

Study Completion Date

October 31, 2013

Conditions
HIV
Interventions
BIOLOGICAL

EN41-FPA2 HIV vaccine

Group 1 Nasal vaccine - Low-dose (20 µg in 40 µL) IM vaccine (200 µg in 400 µL)

BIOLOGICAL

EN41-FPA2 HIV vaccine

Group 2 Nasal vaccine - Mid-dose (100 µg in 200 µL) IM vaccine (200 µg in 400 µL)

BIOLOGICAL

EN41-FPA2 HIV vaccine

Group 3 Nasal vaccine - Full-dose (200 µg in 400 µL) IM vaccine (200 µg in 400 µL)

BIOLOGICAL

EN41-FPA2 HIV vaccine

Group 4 Nasal Placebo - 400 µL IM vaccine (200 µg in 400 µL)

BIOLOGICAL

Na Cl Placebo vaccine

Group 5 Nasal placebo - 40 µL in Cohort 1 / 200 µL in Cohort 2 IM placebo (400 µL)

Trial Locations (1)

GU2 7XP

Surrey Clinical Research Centre University of Surrey, Guildford

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

European Commission

OTHER

lead

PX'Therapeutics

INDUSTRY