Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT05084508 · ClinicalTrials.gov registry record · Phase 2

A Study on the Immune Response and Safety of Various Potencies of an Investigational Chickenpox Vaccine Compared With a Marketed Chickenpox Vaccine, Given to Healthy Children 12 to 15 Months of Age

A Phase 2 study, sponsored by GlaxoSmithKline.

Completed
Registry status
Phase 2
Development phase
800
Enrollment target

NCT05084508 is a Phase 2 study that has completed, run by GlaxoSmithKline. The registered enrollment target is 800 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05084508, a Phase 2 study, has completed, sponsored by GlaxoSmithKline.

COMPLETED
Registry status
Phase 2
Development phase
800 participants
Enrollment target

Study Summary

The purpose of this study is to assess immune response and safety of various potencies of an investigational chickenpox vaccine given to healthy children 12 to 15 months of age.

Interventions

  • BIOLOGICAL Investigational varicella vaccine low potency
  • BIOLOGICAL Investigational varicella vaccine medium potency
  • BIOLOGICAL Investigational varicella vaccine high potency
  • BIOLOGICAL Licensed varicella vaccine Lot 1
  • BIOLOGICAL Licensed varicella vaccine Lot 2

Trial Details

FieldValue
Enrollment Target 800 participants
Start Date 2022-02-03
Est. Completion 2024-06-13
Phase Phase 2

Sponsor

GlaxoSmithKline

1,345 total trials

What the Registry Record Tells You About NCT05084508

The ClinicalTrials.gov registry entry for NCT05084508 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 800 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is GlaxoSmithKline, which has 1,345 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 5 interventions - of which Investigational varicella vaccine low potency is the first listed.

NCT05084508 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT05084508 about?

NCT05084508 is a clinical study titled "A Study on the Immune Response and Safety of Various Potencies of an Investigational Chickenpox Vaccine Compared With a Marketed Chickenpox Vaccine, Given to Healthy Children 12 to 15 Months of Age". The purpose of this study is to assess immune response and safety of various potencies of an investigational chickenpox vaccine given to healthy children 12 to 15 months of age.

What is the current status of trial NCT05084508?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 800 participants. The study started on 2022-02-03. Estimated completion is 2024-06-13.

What interventions are being tested in trial NCT05084508?

The interventions under investigation include: Investigational varicella vaccine low potency (BIOLOGICAL), Investigational varicella vaccine medium potency (BIOLOGICAL), Investigational varicella vaccine high potency (BIOLOGICAL), Licensed varicella vaccine Lot 1 (BIOLOGICAL), Licensed varicella vaccine Lot 2 (BIOLOGICAL).

Who is sponsoring clinical trial NCT05084508?

This trial is sponsored by GlaxoSmithKline, which has 1,345 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.