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Clinical Trial Summary

A phase Ib partially blinded pilot study to evaluate the safety and immunological effects of PENNVAX-B with or without co-administration of constructs containing DNA encoding for the expression of either IL-12 or IL-15.

Primary objectives

1. To determine the safety of HIV-1 DNA constructs (PENNVAX-B).

2. To determine the safety and optimal doses of the IL-12 and the IL-15 adjuvant constructs when given with PENNVAX-B.

Secondary objectives

1. To compare the various vaccine groups for their immunological responses to several HIV-1 antigens, utilizing the ELISPOT assay.

2. To analyze antibody responses to the vaccine antigens over time.

3. To measure CD8 cell proliferative responses to vaccine antigens over time.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00775424
Study type Interventional
Source University of Pennsylvania
Contact
Status Completed
Phase Phase 1
Start date September 2008
Completion date June 2010

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