A Phase 1 Randomized, Placebo-controlled, Double-blind Dose-escalation Trial to Evaluate the Safety and Immunogenicity of tgAAC09, a Gag-PR-RT AAV HIV Vaccine

International AIDS Vaccine Initiative5 sites in 3 countries80 target enrollmentDecember 2003

ConditionsHIV Infection

Overview

Phase: Phase 1
Intervention: Not specified
Conditions: HIV Infection
Sponsor: International AIDS Vaccine Initiative
Enrollment: 80
Locations: 5
Primary Endpoint: Safety of one or two doses of tgAAC09
Status: Completed
Last Updated: 13 years ago

Overview Investigators Eligibility Criteria Outcomes Sites Similar Trials

Overview

Brief Summary

The purpose of this study is to determine safety and immunogenicity (ability to induce an immune response) of a novel HIV vaccine based on adeno-associated virus (AAV)

Detailed Description

The need for a vaccine to prevent AIDS and interrupt transmission of HIV is indisputable. To be effective, an HIV vaccine will have to induce cellular and humoral immune responses that are durable and potent. Intra-muscular delivery of HIV genes enclosed within recombinant adeno-associated virus (rAAV) protein capsid has been shown to be a potent inducer of both antibodies and T-cell responses in animal studies. tgAAC09, consisting of single-stranded DNA from Clade C HIV-1 genes for the gag, protease and part of the reverse transcriptase proteins enclosed within a rAAV serotype 2 protein capsid, was developed as one component of a multi-component HIV vaccine. The purpose of this study is to evaluate the safety and immunogenicity of tgAAC09 in healthy, HIV-seronegative volunteers.

Registry

clinicaltrials.gov

Start Date

December 2003

End Date

January 2007

Last Updated

13 years ago

Study Type

Interventional

Study Design

Factorial

Sex

All

Investigators

Sponsor

International AIDS Vaccine Initiative

Responsible Party

Sponsor

Eligibility Criteria

Inclusion Criteria

•Healthy males and females
•Age at least 18 years on the day of screening and no greater than 50 years on the day of vaccination
•Available for follow-up for the planned duration of the study (screening plus 12 months)
•Able to give written informed consent;
•No reported high-risk behavior for HIV (Appendix C), willing to undergo HIV testing and receive results;
•If sexually active, willing to use or have partner use condoms from screening until at least 4 months after the vaccination. Additional means of contraception are permitted and encouraged.

Exclusion Criteria

•Clinically relevant abnormality on history or examination including history of immunodeficiency or use of immunosuppressive medication in last 6 months;
•A chronic medical condition or concurrent condition, which, in the opinion of the investigator, would make the volunteer unsuitable for the study.
•Any of the following abnormal laboratory parameters that are mild and judged to be clinically significant by the principal investigator or designee, or moderate, severe, or very severe: hematology (hemoglobin, absolute neutrophil count \[ANC\] absolute lymphocyte count \[ALC\], absolute CD4 count, platelets); urinalysis, clinical chemistry (total bilirubin, creatinine, AST, ALT). Refer to Appendix D for the grading of these laboratory parameters.
•If female, pregnant or planning a pregnancy within 4 months after receiving the vaccine, or lactating;
•Receipt of live attenuated vaccine within 60 days or other vaccine within 14 days of vaccination;
•Receipt of other experimental HIV vaccine at any time;
•Receipt of blood transfusion or blood products within 6 months of vaccination;
•Participation in another clinical trial of an investigational product currently or within 12 weeks of vaccination, or expected during participation in this study;
•History of severe local or systemic reaction to vaccination or history of allergic reactions to vaccines;
•Confirmed infection with HIV-1 or HIV-2;