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ACTIVE NOT RECRUITING Phase 2

A Study of mRNA-1345 Vaccine Targeting Respiratory Syncytial Virus in Pregnant Women and in Infants Born to Vaccinated Mothers

NCT06143046 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of the study is to evaluate the reactogenicity, safety, and immunogenicity of an investigational respiratory syncytial virus (RSV) vaccine, mRNA-1345, in pregnant women, and safety and immunogenicity in infants born to vaccinated mothers.

Interventions

  • BIOLOGICAL Placebo
  • BIOLOGICAL mRNA-1345

Study Locations (20)

California

  • Matrix Clinical Research - Gardena — Gardena
  • Matrix Clinical Research - Huntington Park — Huntington Park
  • Matrix Clinical Research, Inc - Corporate Office — Los Angeles

Idaho

  • Clinical Research Prime - ClinEdge - PPDS — Idaho Falls
  • Bingham Memorial Hospital — Pocatello
  • Clinical Research Prime - ClinEdge - Rexburg - PPDS — Rexburg

Montana

  • Boeson Research GTF - Great Falls - ERN - PPDS — Great Falls
  • Boeson Research KAL - Kalispell - ERN - PPDS — Kalispell
  • Boeson Research MSO - Missoula - ERN - PPDS — Missoula

Nebraska

  • Velocity Clinical Research (Grand Island - Nebraska) - PPDS — Grand Island
  • Velocity Clinical Research (Hastings - Nebraska) - PPDS — Hastings
  • Velocity Clinical Research (Norfolk - Nebraska) - PPDS — Norfolk

Arizona

  • Abby's Research Institute — Phoenix
  • Watching Over Mothers & Babies — Tucson

Texas

  • DM Clinical Research - Bellaire - ERN - PPDS — Houston
  • Maximos OB/GYN — League City

Alabama

  • SEC Clinical Research LLC - Dothan 2 - ClinEdge - PPDS — Dothan

Arkansas

  • Applied Research Center of Arkansas - ClinEdge - PPDS — Little Rock

Trial Details

FieldValue
Enrollment Target 360 participants
Start Date 2023-11-15
Est. Completion 2026-05-27
Phase Phase 2

Sponsor

ModernaTX

67 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06143046

The ClinicalTrials.gov registry entry for NCT06143046 describes a study currently listed as active not recruiting. It is categorized as Phase 2, 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 360 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 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: NCT06143046 reports 20 study locations spanning 10 distinct geographic areas — top geographies include California, Idaho, Montana. 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 NCT06143046 about?

NCT06143046 is a clinical study titled "A Study of mRNA-1345 Vaccine Targeting Respiratory Syncytial Virus in Pregnant Women and in Infants Born to Vaccinated Mothers". The purpose of the study is to evaluate the reactogenicity, safety, and immunogenicity of an investigational respiratory syncytial virus (RSV) vaccine, mRNA-1345, in pregnant women, and safety and immunogenicity in infants born to vaccinated mothers.

What is the current status of trial NCT06143046?

This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 360 participants. The study started on 2023-11-15. Estimated completion is 2026-05-27.

What conditions does trial NCT06143046 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 NCT06143046?

The interventions under investigation include: Placebo (BIOLOGICAL), mRNA-1345 (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06143046?

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 NCT06143046 being conducted?

This trial has 20 study locations across Alabama, Arizona, Arkansas, California, Idaho. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial