Pilot Study of 4-18F- Fluoro-1-naphthol PET/CT for Chronic Graft Versus Host Disease

This study is looking at the safety and potential side effects of an imaging agent called 4-\[18F\]Fluoro-1-Naphthol (or \[18F\]4FN) when used with PET/CT scans. This is for people who have chronic graft versus host disease (GVHD), a condition where donated cells attack the patient's body. Researchers want to see if the images from \[18F\]4FN PET/CT can show where and how severe your chronic GVHD is, especially in your joints. They also want to see if these images can predict GVHD before symptoms appear. You can join if you are 18 or older, have chronic GVHD affecting your joints, and meet other health requirements. The study aims to see if this imaging method works as expected. The current recruitment status is unclear.

Study design
This is an interventional pilot study with a planned enrollment of 16 participants. It is not specified if it is randomized or blinded.
What's involved
Participants will receive \[18F\]4FN by IV and undergo PET-CT imaging. The primary endpoint for safety will be measured through study completion, an average of 1 year.
Compensation
Not stated in the trial record.
Follow-up
Safety and adverse events will be monitored through study completion, which is an average of 1 year.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07325253

A Pilot Study to Correlate 4-18F- Fluoro-1-naphthol 18F-4FN PET/CT Imaging With Graft Versus Host Disease Manifestations

Recruiting
PHASE2Ages 18+InterventionalDiagnostic
M.D. Anderson Cancer Center
~16 participants
Updated 2026-09-17 on ClinicalTrials.gov
What's tested:[18F]-4FNPET-CT

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Safety and adverse events (AEs).
Measured over Through study completion; an average of 1 year.
Pilot Study
PET/CT Imaging
Host Disease Manifestation

NCT07325253

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • MD Anderson Cancer Center

    Houston, Texasstudy coordinator listed

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

  • George L Chen, MD · PRINCIPAL_INVESTIGATOR · M.D. Anderson Cancer Center

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  • Safety and adverse events (AEs).Through study completion; an average of 1 year.

    Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0