CI

At a glance

ClinicalIndex Comparison Record
Phase 1Active· 10 enrolled
Drug / intervention
VRC-HIVAAV070-00-GT (AAV8-VRC07)genetic
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03374202
NCT03374202Phase 1Active

VRC 603: A Phase I Dose-Escalation Study of the Safety of AAV8-VRC07 (VRC-HIVAAV070-00-GT) Recombinant AAV Vector Expressing VRC07 HIV-1 Neutralizing Antibody in Antiretroviral-Treated, HIV-1 Infected Adults With Controlled Viremia

National Institute of Allergy and Infectious Diseases (NIAID)·interventional·Posted Dec 15, 2017·Updated Apr 27, 2025

In Brief

A Phase 1 clinical trial evaluating VRC-HIVAAV070-00-GT (AAV8-VRC07) for HIV-1 Infected Adults With Controlled Viremia. Active but no longer recruiting, targeting 10 participants across 1 site.

Detailed Summary

Background: The Human Immunodeficiency Virus (HIV) attacks the immune system. Scientists have created a gene that could be transferred to the cells of people with HIV. The gene should tell the cells to make an antibody called VRC07. This antibody fights HIV. The VRC07 gene is packaged into a man-made version of a virus called AAV8. Objectives: To see if AAV8-VRC07 is safe. To study if it causes cells to produce the VRC07 antibody. Eligibility: Adults ages 18-65 who are HIV infected but in general good health and have been taking the same HIV medicine for at least 3 months Design: Participants were screened in a different protocol. Participants received the study product on day 1. It was injected one or more times in the upper arm or thigh using a needle. Participants weight was measured to calculate the dose. Women may have had a pregnancy test. For 7 days after getting the study product, participants checked their temperature with a thermometer. They noted any symptoms in an electronic or paper diary. Participants will have study visits. At each one, they will have a physical exam and medical history. They will have blood drawn and may have saliva collected. The study visit schedule is as follows: For 12 weeks: 1 visit a week For the next 12 weeks: 1 visit every other week Then about 1 visit a month After 1 year in the study: a visit every 6 months for the next 4 years. Total study participation is 5 years.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 1Active
201820192020202120222023202420252026
First PostedDec 15, 2017
Enrollment StartJan 11, 2018
Primary CompletionAug 8, 2026
TodayJul 2, 2026
Enrollment to primary: 8.6 yearsPosted 8.5 years agoPrimary completion in 1 month

Interventions

VRC-HIVAAV070-00-GT (AAV8-VRC07)genetic

AAV8-VRC07 is a recombinant AAV vector expressing a HIV-1 CD4 binding site-specific neutralizing antibody, VRC07