CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 1 enrolled
Drug / intervention
AIDSVAX® B/Ebiological
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/NCT03618056
NCT03618056Phase 1Completed

A Phase 1b Open Label Clinical Trial to Evaluate HIV-1 Neutralization Antibody Breadth in Response to HIV gp120 Protein Vaccine in HIV-uninfected Adults With Quiescent Systemic Lupus Erythematosus

National Institute of Allergy and Infectious Diseases (NIAID)·interventional·Posted Aug 7, 2018·Updated Feb 7, 2022

In Brief

A Phase 1 clinical trial evaluating AIDSVAX® B/E for HIV Infections and Systemic Lupus Erythematosus. Completed, enrolled 1 participant across 1 site.

Detailed Summary

The purpose of this study is to evaluate the breadth and potency of HIV-1 neutralizing antibody (nAb) responses and examine the safety and tolerability of an HIV gp120 protein vaccine (AIDSVAX® B/E) in HIV-uninfected adults diagnosed with Systemic Lupus Erythematosus (SLE) who have stable disease.

Study Details

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

Timeline

Phase 1CompletedFinished
20192020202120222023202420252026
First PostedAug 7, 2018
Enrollment StartDec 19, 2018
Primary CompletionJul 17, 2020
TodayJul 2, 2026
Enrollment to primary: 1.6 yearsPosted 7.9 years ago

Interventions

AIDSVAX® B/Ebiological

Administered by intramuscular injection