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NCT03220724 · ClinicalTrials.gov registry record · Phase 1

Evaluating the Safety and Immunogenicity of EnvSeq-1 and CH505 M5 gp120 Envs Adjuvanted With GLA-SE in Healthy, HIV-Uninfected Adults

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

Completed
Registry status
Phase 1
Development phase
117
Enrollment target

NCT03220724 is a Phase 1 study that has completed, run by National Institute of Allergy and Infectious Diseases (NIAID). The registered enrollment target is 117 participants.

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The verdict

NCT03220724, a Phase 1 study, has completed, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

COMPLETED
Registry status
Phase 1
Development phase
117 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the safety, tolerability, and immunogenicity of EnvSeq-1 and CH505 M5 gp120 Envs adjuvanted with GLA-SE in healthy, HIV-uninfected adults.

Interventions

  • BIOLOGICAL GLA-SE adjuvant
  • BIOLOGICAL CH505TF
  • BIOLOGICAL CH505w53
  • BIOLOGICAL CH505w78
  • BIOLOGICAL CH505 M5

Trial Details

FieldValue
Enrollment Target 117 participants
Start Date 2017-08-22
Est. Completion 2023-03-21
Phase Phase 1

What the Registry Record Tells You About NCT03220724

The ClinicalTrials.gov registry entry for NCT03220724 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 117 participants, a figure that helps gauge the scale of data the investigators plan to collect. 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 0 conditions, and to 5 interventions - of which GLA-SE adjuvant is the first listed.

NCT03220724 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03220724 about?

NCT03220724 is a clinical study titled "Evaluating the Safety and Immunogenicity of EnvSeq-1 and CH505 M5 gp120 Envs Adjuvanted With GLA-SE in Healthy, HIV-Uninfected Adults". The purpose of this study is to evaluate the safety, tolerability, and immunogenicity of EnvSeq-1 and CH505 M5 gp120 Envs adjuvanted with GLA-SE in healthy, HIV-uninfected adults.

What is the current status of trial NCT03220724?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 117 participants. The study started on 2017-08-22. Estimated completion is 2023-03-21.

What interventions are being tested in trial NCT03220724?

The interventions under investigation include: GLA-SE adjuvant (BIOLOGICAL), CH505TF (BIOLOGICAL), CH505w53 (BIOLOGICAL), CH505w78 (BIOLOGICAL), CH505 M5 (BIOLOGICAL).

Who is sponsoring clinical trial NCT03220724?

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

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

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.