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A Safety and Immune Response Study to Evaluate Varying Doses of an mRNA Vaccine Against Coronavirus Disease 2019 (COVID-19) in Healthy Adults
NCT05972993 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to evaluate the safety, reactogenicity and immune responses of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) mRNA-CR-04 vaccine construct when administered in healthy adults previously vaccinated with SARS-CoV-2 mRNA vaccines.
Conditions Studied
Interventions
- DRUG Placebo
- BIOLOGICAL mRNA-CR-04 vaccine 10μg
- BIOLOGICAL mRNA-CR-04 vaccine 30μg
- BIOLOGICAL mRNA-CR-04 vaccine 100μg
- BIOLOGICAL mRNA-CR-04 vaccine 3μg
Study Locations (4)
California
- GSK Investigational Site — San Diego
Florida
- GSK Investigational Site — Melbourne
Illinois
- GSK Investigational Site — Peoria
Texas
- GSK Investigational Site — Austin
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 114 participants |
| Start Date | 2023-08-07 |
| Est. Completion | 2024-10-14 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05972993
The ClinicalTrials.gov registry entry for NCT05972993 describes a study currently listed as completed. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 114 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is GlaxoSmithKline, which has 558 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with COVID-19 appearing as the primary indexed condition, and to 5 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT05972993 reports 4 study locations spanning 4 distinct geographic areas — top geographies include California, Florida, Illinois. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT05972993 about?
NCT05972993 is a clinical study titled "A Safety and Immune Response Study to Evaluate Varying Doses of an mRNA Vaccine Against Coronavirus Disease 2019 (COVID-19) in Healthy Adults". The purpose of this study is to evaluate the safety, reactogenicity and immune responses of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) mRNA-CR-04 vaccine construct when administered in healthy adults previously vaccinated with SARS-CoV-2 mRNA vaccines.
What is the current status of trial NCT05972993?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 114 participants. The study started on 2023-08-07. Estimated completion is 2024-10-14.
What conditions does trial NCT05972993 study?
This clinical trial studies the following conditions: COVID-19. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT05972993?
The interventions under investigation include: Placebo (DRUG), mRNA-CR-04 vaccine 10μg (BIOLOGICAL), mRNA-CR-04 vaccine 30μg (BIOLOGICAL), mRNA-CR-04 vaccine 100μg (BIOLOGICAL), mRNA-CR-04 vaccine 3μg (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT05972993?
This trial is sponsored by GlaxoSmithKline, which has 558 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT05972993 being conducted?
This trial has 4 study locations across California, Florida, Illinois, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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