Could a simple scan reveal which cancers are hiding a dangerous protein?
NCT ID NCT07301814
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a new PET imaging probe that targets a protein called CLDN18.2, found in some stomach, pancreatic, bile duct, and esophageal cancers. Researchers will scan 56 people (patients and healthy volunteers) to see if the scan can accurately detect tumors and guide treatment choices. The goal is to improve diagnosis and help doctors decide who should receive CLDN18.2-targeted therapies.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- CLDN18.2-specific PET imaging probe (a radioactive tracer)
- What this could lead to
- If successful, this imaging method could help doctors better identify which patients might benefit from CLDN18.2-targeted therapies, improving personalized cancer treatment.
- What could go wrong
- This is an early-stage imaging study with only 56 participants, so results may not apply broadly. The tracer's safety and accuracy are still being evaluated.
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.
- Participants
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About 56 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2025
- Expected to finish
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Dec 2026
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.
Who is studied
Patients with suspected or confirmed malignant tumors such as gastric adenocarcinoma, pancreatic cancer, bile duct cancer, esophageal adenocarcinoma, etc. (supporting evidence includes serum tumor markers, ultrasound, CT, MRI, and histopathological examination of tissue, etc.), and in good general condition.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * Each participant must meet all inclusion criteria to be eligible to participate in the study: 1. The participant or their legal representative is able to sign the informed consent form with signature and date; 2. Commit to adhering to the research procedures and cooperating in the implementation of the entire research process; 3. Adult patients or healthy volunteers (aged 18-70 years), male or female; 4. Patients with malignant tumors such as gastric cancer, pancreatic cancer, bile duct cancer, esophageal cancer, etc., suspected or diagnosed clinically (supporting evidence includes serum tumor markers, ultrasound, CT, MRI, and other imaging data, as well as histopathological examination), and in good general condition; 5. Meet specific laboratory test results; 6. Women of childbearing age must use contraception for at least one month before screening and commit to using contraception throughout the study period and continuing it until the specified time after the study ends; 7. Other set inclusion criteria. Exclusion Criteria: * All subjects who meet any exclusion criteria baseline will be excluded from the study: 1. Those unable to complete PET/MR or PET/CT scans (including those unable to lie flat, claustrophobia, radiation phobia, etc.); 2. Those with other comorbidities; 3. Patients known to be allergic to the targeted CLDN18.2 PET imaging agent or synthetic excipients; fasting blood glucose level exceeding 11.0 mmol/L before injection of 18F-FDG; 4. Those with a history of concomitant medication use; 5. Patients considered to have poor compliance by the researcher.
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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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Wuhan Union Hospital, China
RECRUITINGWuhan, Hubei, 430030, China
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