PET scan lights up lung scarring to guide treatment
NCT ID NCT06189820
First seen Oct 16, 2026 · Last updated Oct 16, 2026
Summary
Researchers are testing a PET/CT scan that uses a tracer called FAPI to measure fibrotic activity in the lungs of adults with pulmonary fibrosis. The study checks whether lung FAPI uptake drops after patients start anti-fibrotic treatment, and whether those changes match clinical outcomes like lung function decline. About 70 participants will receive the scan, which involves an intravenous tracer injection followed by imaging.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- FAPI PET/CT imaging with 18F-FAPI-74 or 68Ga-FAPI-46 tracer
- What this could lead to
- If it works, doctors could use FAPI PET/CT scans to see whether anti-fibrotic drugs are slowing lung scarring, helping them adjust treatment sooner.
- What could go wrong
- The tracer may not reliably measure fibrosis changes, and the small size means results might not apply broadly. PET scans also involve radiation and are not risk-free.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 70 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2023
- Expected to finish
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Mar 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adults patients with a fibrotic lung disease (idiopathic pulmonary fibrosis (IPF) or non-IPF fibrotic ILD) as defined according to the 2022 ATS/ERS/JRS/ALAT Clinical Practice Guidelines Exclusion Criteria: * Pregnant or nursing patients * Patients with another significant medical condition which, in the investigator's opinion, may interfere with the completion of the study. * Patients with an active lung neoplasm or any active neoplasm for blood samples
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Medecine
RECRUITINGBrussels, 1070, Belgium
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