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NCT06071767 · ClinicalTrials.gov registry record · Phase 1

Evaluation of Safety, Immunogenicity and Efficacy of a Triple Immune Regimen in Adults Initiated on ART During Acute HIV-1

A Phase 1 study of HIV-1-infection, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

Recruiting
Registry status
Phase 1
Development phase
36
Enrollment target
12
Study locations

NCT06071767 is a Phase 1 study of HIV-1-infection that is actively recruiting participants, run by National Institute of Allergy and Infectious Diseases (NIAID). The registered enrollment target is 36 participants, below the 351-participant average among 71 other HIV-1-infection trials with a reported enrollment target (90% lower). The trial reports 12 study locations across 12 states.

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The verdict

NCT06071767, a Phase 1 study of HIV-1-infection, is actively recruiting participants, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

RECRUITING
Registry status
Phase 1
Development phase
36 participants
Enrollment target
12
Study locations

Study Summary

The purpose of this study is to evaluate the safety, tolerability, and efficacy of therapeutic vaccination with chimpanzee adenovirus ChAdOx1- and poxvirus modified vaccinia Ankara (MVA)-vectored conserved mosaic T-cell vaccines in a sequential regimen with the toll-like receptor 7 (TLR7) agonist vesatolimod (VES) and two broadly neutralizing antibodies (bNAbs) compared to placebo, to induce HIV-1 control during analytic treatment interruption (ATI).

Conditions Studied

Interventions

  • BIOLOGICAL ChAdOx1.tHIVconsv1
  • BIOLOGICAL ChAdOx1.HIVconsv62
  • BIOLOGICAL MVA.tHIVconsv3
  • BIOLOGICAL MVA.tHIVconsv4
  • DRUG Vesatolimod (VES)

Study Locations (12)

California

  • University of California, San Diego AntiViral Research Center CRS - San Diego

Georgia

  • Ponce de Leon Center CRS - Atlanta

Illinois

  • Northwestern University CRS - Chicago

Massachusetts

  • Massachusetts General Hospital CRS (MGH CRS) - Boston

Missouri

  • Washington University Therapeutics CRS - St Louis

New York

  • Columbia Physicians & Surgeons CRS - New York

North Carolina

  • Chapel Hill CRS - Chapel Hill

Ohio

  • Ohio State University CRS - Columbus

Trial Details

FieldValue
Enrollment Target 36 participants
Start Date 2024-04-01
Est. Completion 2029-08-01
Phase Phase 1

What the Registry Record Tells You About NCT06071767

The ClinicalTrials.gov registry entry for NCT06071767 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 36 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 351-participant average among 71 other HIV-1-infection trials with a reported enrollment target (90% lower). The listed sponsor is National Institute of Allergy and Infectious Diseases (NIAID), which has 2,006 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with HIV-1-infection appearing as the primary indexed condition, and to 5 interventions - of which ChAdOx1.tHIVconsv1 is the first listed.

NCT06071767 reports 12 study locations spanning 12 distinct geographic areas - top geographies include California, Georgia, Illinois.

Frequently Asked Questions

What is clinical trial NCT06071767 about?

NCT06071767 is a clinical study titled "Evaluation of Safety, Immunogenicity and Efficacy of a Triple Immune Regimen in Adults Initiated on ART During Acute HIV-1". The purpose of this study is to evaluate the safety, tolerability, and efficacy of therapeutic vaccination with chimpanzee adenovirus ChAdOx1- and poxvirus modified vaccinia Ankara (MVA)-vectored conserved mosaic T-cell vaccines in a sequential regimen with the toll-like receptor 7 (TLR7) agonist ve...

What is the current status of trial NCT06071767?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 36 participants. The study started on 2024-04-01. Estimated completion is 2029-08-01.

What conditions does trial NCT06071767 study?

This clinical trial studies the following conditions: HIV-1-infection.

What interventions are being tested in trial NCT06071767?

The interventions under investigation include: ChAdOx1.tHIVconsv1 (BIOLOGICAL), ChAdOx1.HIVconsv62 (BIOLOGICAL), MVA.tHIVconsv3 (BIOLOGICAL), MVA.tHIVconsv4 (BIOLOGICAL), Vesatolimod (VES) (DRUG).

Who is sponsoring clinical trial NCT06071767?

This trial is sponsored by National Institute of Allergy and Infectious Diseases (NIAID), which has 2,006 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06071767 being conducted?

This trial has 12 study locations across California, Georgia, Illinois, Massachusetts, Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.