ClinicalTrials.gov record
Completed Phase 2 Interventional Accepts healthy volunteers Results available

A Study on the Safety and Immune Response of Investigational COVID-19 mRNA Vaccines in Healthy Adults

ClinicalTrials.gov ID: NCT05960097

Public ClinicalTrials.gov record NCT05960097. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 5, 2026, 4:48 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2 Randomized, Active-controlled, Observer-blind Study to Assess the Safety, Reactogenicity, and Immunogenicity of a Booster Dose of Investigational COVID-19 mRNA Vaccines in Healthy Adults Who Previously Received a Complete Primary Vaccination Series With or Without Booster Dose(s)

Study identification

NCT ID
NCT05960097
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
692 participants

Conditions and interventions

Interventions

  • CV0601 mRNA COVID-19 Vaccine Biological
  • CV0701 mRNA COVID-19 Vaccine (High dose) Biological
  • CV0701 mRNA COVID-19 Vaccine (Low dose) Biological
  • CV0701 mRNA COVID-19 Vaccine (Medium dose) Biological
  • CV0801 mRNA COVID-19 Vaccine Biological
  • Control vaccine Biological

Biological

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 31, 2023
Primary completion
Aug 29, 2024
Completion
Aug 29, 2024
Last update posted
Oct 22, 2025

2023 – 2024

United States locations

U.S. sites
3
U.S. states
3
U.S. cities
3
Facility City State ZIP Site status
GSK Investigational Site Sacramento California 95864
GSK Investigational Site Hollywood Florida 33024
GSK Investigational Site Peoria Illinois 61614-4896

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 14 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05960097, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 22, 2025 · Synced May 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05960097 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →