A Trial to Evaluate the Safety and Tolerability of DV700P-RNA and DV701B1.1-RNA Immunization in Combination With Antiretroviral Analytical Treatment Interruption (ATI) in People Living With HIV for Elicitation of V3-glycan Antibodies

ConditionHIV
Trial statusNot yet recruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18-60
SponsorNational Institute of Allergy and Infectious Diseases (NIAID)

About this trial

This phase 1 study will evaluate the safety, tolerability, and immune responses of two experimental mRNA HIV vaccines in adults living with HIV who are in overall good health. The study will enroll about 42 participants at multiple study sites. Researchers will assess whether these vaccines can start or strengthen antibody responses against HIV. The study will also evaluate how a closely monitored planned pause in antiretroviral therapy affects these immune responses.

Eligibility criteria

Qualifiers

Able and willing to provide informed consent.

Age 18 to 60 years.

Documented HIV infection.

Lowest (nadir) CD4+ count between 250 and 450 cells/mm³.

Disqualifiers

Current use of ART that includes non-nucleoside reverse transcriptase inhibitors (NNRTIs).

Use of long-acting ART within 3 months prior to enrollment.

Known resistance to any component of the current ART regimen (excluding M184V/I mutation).

Resistance to one or more drugs in two or more ART classes (excluding M184V/I mutation).

Trial design

Treatments tested in this trial

  • DV700P-RNA 100 mcg
  • DV701B1.1-RNA 100 mcg

Treatment groups

42 Participants
are divided into 2 treatment groups

Sponsors and collaborators

National Institute of Allergy and Infectious Diseases (NIAID)

Lead sponsor

Department of Health and Human Services

Collaborator

Duke University

Collaborator