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A Study to Investigate the Immunogenicity and Safety of mRNA-1345 Vaccine Targeting Respiratory Syncytial Virus (RSV) in High-risk Adults
NCT06067230 · View on ClinicalTrials.gov ↗
Study Summary
The study is divided into 2 parts (Part A and Part B). Part A of the study will evaluate the safety and immune response to mRNA-1345 in high-risk adults aged ≥18 to \<60 years. Part B of the study will evaluate the safety and immune response to mRNA-1345 in adults who received solid organ transplant (SOT).
Conditions Studied
Interventions
- BIOLOGICAL mRNA-1345
Study Locations (20)
Arizona
- Lenzmeier Family Medicine - CCT - PPDS — Glendale
- Foothills Research Center - CCT - PPDS — Phoenix
- Fiel Family & Sports Medicine - PC - CCT - PPDS — Tempe
Florida
- Excel Medical Clinical Trials DBA Flourish — Boca Raton
- Indago Research and Health Center — Hialeah
- CenExel RCA - Hollywood — Hollywood
California
- David Geffen School of Medicine at UCLA — Los Angeles
- Artemis Institute For Clinical Research LLC - San Diego - Headlands - PPDS — San Diego
Illinois
- University of Chicago — Chicago
- AES - DRS - Optimal Research Illinois - Peoria — Peoria
Michigan
- Henry Ford Hospital — Detroit
- DM Clinical Research - Southfield - ERN - PPDS — Southfield
Arkansas
- Baptist Health Center for Clinical Research — Little Rock
Colorado
- Critical Care, Pulmonary and Sleep Associates / CCT Research — Lakewood
Connecticut
- Yale University School of Medicine — New Haven
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,153 participants |
| Start Date | 2023-10-06 |
| Est. Completion | 2026-07-30 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06067230
The ClinicalTrials.gov registry entry for NCT06067230 describes a study currently listed as active not recruiting. 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 1,153 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 Respiratory Syncytial Virus appearing as the primary indexed condition, and to 1 intervention — of which mRNA-1345 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: NCT06067230 reports 20 study locations spanning 13 distinct geographic areas — top geographies include Arizona, Florida, California. 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 NCT06067230 about?
NCT06067230 is a clinical study titled "A Study to Investigate the Immunogenicity and Safety of mRNA-1345 Vaccine Targeting Respiratory Syncytial Virus (RSV) in High-risk Adults". The study is divided into 2 parts (Part A and Part B). Part A of the study will evaluate the safety and immune response to mRNA-1345 in high-risk adults aged ≥18 to \<60 years. Part B of the study will evaluate the safety and immune response to mRNA-1345 in adults who received solid organ transplan...
What is the current status of trial NCT06067230?
This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 1,153 participants. The study started on 2023-10-06. Estimated completion is 2026-07-30.
What conditions does trial NCT06067230 study?
This clinical trial studies the following conditions: Respiratory Syncytial Virus. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06067230?
The interventions under investigation include: mRNA-1345 (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06067230?
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 NCT06067230 being conducted?
This trial has 20 study locations across Arizona, Arkansas, California, Colorado, Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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