HIV Infections Clinical Trial
Official title:
Evaluation of the Safety of a Polyvalent Vaccinia Virus HIV-1 Envelope Recombinant Vaccine (PolyEnv1) in Healthy Adults
The purpose of the study is to determine the safety of a new HIV vaccine and to evaluate the immune response to the vaccine. Only some HIV genes are used to make the vaccine and therefore the vaccine cannot itself cause HIV or AIDS.
HIV-1 presents several challenges to vaccine design, including: 1) high mutation rates
resulting in tremendous diversity of virus envelope, the target of neutralizing antibody,
such that antibody elicited to one envelope may not protect from virus with a distinct
envelope; 2) envelope from infected persons differs from envelopes obtained from T-cell line
cultures, the usual source of envelope for vaccines; and 3) envelope glycoprotein exists as
oligomers on the virion surface, not as the monomers used in previous vaccines. This study
will test a new vaccine that has been designed to meet these challenges by delivering
diverse, patient-derived, oligomeric envelopes to induce multiple type-specific responses
capable of recognizing native envelope on natural variants. The vaccine vector used in this
vaccine trial is recombinant vaccinia virus based on the NYCDH vaccinia isolate.
Participants in this study will receive the PolyEnv1 HIV vaccine and will be followed for
one year. Laboratory tests will be performed at 10 study visits to monitor the participants'
immunologic response and assess the safety of the vaccine. Patients will also have numerous
HIV tests throughout the study period.
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Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention
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