Investigating Immunisation Strategies of DNA, MVA and CN54rgp140 Adjuvanted With GLA-AF to Maximise Antibody Responses

PHASE1CompletedINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

June 30, 2013

Primary Completion Date

January 31, 2014

Study Completion Date

December 31, 2015

Conditions
HIV
Interventions
BIOLOGICAL

DNA

8mg DNA: one plasmid encoding a gag-pol-nef polypeptide derived from the 96ZM651-8 clone and one plasmid encoding gp140 env derived from clade C 97CN54

BIOLOGICAL

MVA-C

1.108 TCID50 MVA-C (nominal titre) expressing the gag-pol-nef and gp120 env proteins derived from clade C 97CN54

BIOLOGICAL

CN54rgp140

100ug CN54rgp140, a trimeric recombinant envelope protein derived from clade C 97CN54

BIOLOGICAL

GLA-AF

5ug GLA-AF, an aqueous glucopyranosyl lipid A adjuvant

Trial Locations (2)

GU2 7XP

Surrey Clinical Research Centre, University of Surrey, Guildford

W2 1PG

Imperial College London, Greater London

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Medical Research Council

OTHER_GOV

collaborator

Wellcome Trust

OTHER

lead

Imperial College London

OTHER

NCT01922284 - Investigating Immunisation Strategies of DNA, MVA and CN54rgp140 Adjuvanted With GLA-AF to Maximise Antibody Responses | Biotech Hunter | Biotech Hunter