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A Study to Evaluate Efficacy, Safety, and Immunogenicity of mRNA-1273 Vaccine in Adults Aged 18 Years and Older to Prevent COVID-19
NCT04470427 · View on ClinicalTrials.gov ↗
Study Summary
The mRNA-1273 vaccine is being developed to prevent COVID-19, the disease resulting from Severe Acute Respiratory Syndrome coronavirus (SARS-CoV-2) infection. The study is designed to primarily evaluate the efficacy, safety, and immunogenicity of mRNA-1273 to prevent COVID-19 for up to 2 years after the second dose of mRNA-1273.
Conditions Studied
Interventions
- BIOLOGICAL Placebo
- BIOLOGICAL mRNA-1273
Study Locations (20)
California
- Advanced Clinical Research - Rancho Paseo — Banning
- University of California San Diego — La Jolla
- eStudySite - La Mesa — La Mesa
- UCLA Vine Street Clinic CRS — Los Angeles
- VA Greater Los Angeles Healthcare (veterans only) — Los Angeles
- Paradigm Clinical Research Institute Inc — Redding
- Benchmark Research - Sacramento — Sacramento
- Medical Center For Clinical Research - M3 Wake Research — San Diego
Arizona
- Hope Research Institute — Chandler
- Synexus Clinical Research US, Inc. - Phoenix West — Glendale
- Hope Research Institute — Peoria
- Hope Research Institute — Phoenix
- Quality of Life Medical and Research Center — Tucson
Alabama
- Ascension St. Vincent Birmingham — Birmingham
- Synexus Clinical Research US, Inc. - Birmingham — Birmingham
Colorado
- University of Colorado Hospital — Aurora
- Lynn Institute of The Rockies — Colorado Springs
Arkansas
- Baptist Health Center for Clinical Research — Little Rock
District of Columbia
- George Washington University — Washington D.C.
Florida
- Accel Research Site — DeLand
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 30,415 participants |
| Start Date | 2020-07-27 |
| Est. Completion | 2022-12-29 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04470427
The ClinicalTrials.gov registry entry for NCT04470427 describes a study currently listed as completed. It is categorized as Phase 3, 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 30,415 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is ModernaTX, which has 67 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 SARS-CoV-2 appearing as the primary indexed condition, and to 2 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: NCT04470427 reports 20 study locations spanning 7 distinct geographic areas — top geographies include California, Arizona, Alabama. 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 NCT04470427 about?
NCT04470427 is a clinical study titled "A Study to Evaluate Efficacy, Safety, and Immunogenicity of mRNA-1273 Vaccine in Adults Aged 18 Years and Older to Prevent COVID-19". The mRNA-1273 vaccine is being developed to prevent COVID-19, the disease resulting from Severe Acute Respiratory Syndrome coronavirus (SARS-CoV-2) infection. The study is designed to primarily evaluate the efficacy, safety, and immunogenicity of mRNA-1273 to prevent COVID-19 for up to 2 years after...
What is the current status of trial NCT04470427?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 30,415 participants. The study started on 2020-07-27. Estimated completion is 2022-12-29.
What conditions does trial NCT04470427 study?
This clinical trial studies the following conditions: SARS-CoV-2. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT04470427?
The interventions under investigation include: Placebo (BIOLOGICAL), mRNA-1273 (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT04470427?
This trial is sponsored by ModernaTX, which has 67 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT04470427 being conducted?
This trial has 20 study locations across Alabama, Arizona, Arkansas, California, Colorado. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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