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RECRUITING Phase 2

A Study Evaluating Persistence of the Immune Response of the Adjuvanted Respiratory Syncytial Virus (RSV) Vaccine and the Safety and Immune Response Following Revaccination in Adults 18 Years of Age and Above Who Received Lung or Kidney Transplant

NCT07092865 · View on ClinicalTrials.gov ↗

Study Summary

This study evaluates persistence of the immune response of the adjuvanted RSV vaccine and the safety and immunogenicity following revaccination in adults 18 years of age and above who received lung or kidney transplant.

Interventions

  • BIOLOGICAL Adjuvanted RSVPreF3 vaccine

Study Locations (20)

Other

  • GSK Investigational Site — Giessen
  • GSK Investigational Site — Milan
  • GSK Investigational Site — Milan
  • GSK Investigational Site — Pavia
  • GSK Investigational Site — Siena
  • GSK Investigational Site — Aichi

Missouri

  • GSK Investigational Site — St Louis
  • GSK Investigational Site — St Louis

Queensland

  • GSK Investigational Site — Birtinya
  • GSK Investigational Site — Herston

Ontario

  • GSK Investigational Site — London
  • GSK Investigational Site — Toronto

Kentucky

  • GSK Investigational Site — Lexington

Nebraska

  • GSK Investigational Site — Omaha

New York

  • GSK Investigational Site — New York

Pennsylvania

  • GSK Investigational Site — Pittsburgh

Trial Details

FieldValue
Enrollment Target 184 participants
Start Date 2025-08-06
Est. Completion 2027-07-16
Phase Phase 2

Sponsor

GlaxoSmithKline

558 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07092865

The ClinicalTrials.gov registry entry for NCT07092865 describes a study currently listed as 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 184 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 Respiratory Syncytial Virus Infections appearing as the primary indexed condition, and to 1 intervention — of which Adjuvanted RSVPreF3 vaccine 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: NCT07092865 reports 20 study locations spanning 12 distinct geographic areas — top geographies include Other, Missouri, Queensland. 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 NCT07092865 about?

NCT07092865 is a clinical study titled "A Study Evaluating Persistence of the Immune Response of the Adjuvanted Respiratory Syncytial Virus (RSV) Vaccine and the Safety and Immune Response Following Revaccination in Adults 18 Years of Age and Above Who Received Lung or Kidney Transplant". This study evaluates persistence of the immune response of the adjuvanted RSV vaccine and the safety and immunogenicity following revaccination in adults 18 years of age and above who received lung or kidney transplant.

What is the current status of trial NCT07092865?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 184 participants. The study started on 2025-08-06. Estimated completion is 2027-07-16.

What conditions does trial NCT07092865 study?

This clinical trial studies the following conditions: Respiratory Syncytial Virus Infections. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07092865?

The interventions under investigation include: Adjuvanted RSVPreF3 vaccine (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07092865?

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 NCT07092865 being conducted?

This trial has 20 study locations across Kentucky, Missouri, Nebraska, New York, Pennsylvania. 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