New scan could spot brain tumors more clearly
NCT ID NCT06055790
First seen Jun 24, 2026 · Last updated Jun 26, 2026 · Updated 2 times
Summary
This study tests a special PET/CT scan using a tracer called 18F-Fluciclovine to see if it can better detect brain metastases and tell them apart from changes caused by earlier treatments. About 20 adults with known or suspected brain metastases will get the scan before and after treatment. The goal is to improve diagnosis and monitoring of brain tumors.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- 18F-Fluciclovine (Axumin) – a radioactive tracer used in PET/CT scans
- What this could lead to
- If successful, this scan could help doctors more accurately identify brain metastases and tell them apart from harmless post-treatment changes, improving treatment decisions.
- What could go wrong
- This is a small early-phase study with only 20 participants, so results may not apply to everyone. The scan is not yet proven to be better than current standard methods.
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 20 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2024
- Expected to finish
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Oct 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.
- Ages
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18 to 99 years
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Patients with clinically suspected or diagnosed brain metastatic lesion(s) 2. Age ≥ 18 years 3. Known history cancer 4. Brain MRI in the past 2 months positive for metastatic disease 5. Scheduled for treatment: Surgical resection, or stereotactic radiosurgery, or whole brain radiation therapy. 6. Can tolerate 18F-fluciclovine PET/CT exam (can lie still on their back for the duration of the scan) 7. Ability to understand and the willingness to sign a written informed consent Exclusion Criteria: 1. Patients who do not meeting inclusion criteria. 2. Patients who have had a brain biopsy of the index lesion(s) sooner than 4 weeks from the brain 18F-fluciclovine PET/CT (to minimize false positive uptake due to inflammation). 3. Patients who have had prior brain surgery or radiation treatment of the index lesion(s). 4. Patients who have had treatment of the index brain lesion(s) or initiation of systemic therapy after the last MRI and prior to the PET/CT scan. 5. Prior history of localized brain treatment (surgery or stereotactic radiosurgery /fractionated stereotactic radiotherapy) allowed, if at least one index lesion is not adjacent to previous treatment (10% isodose line of prior RT). Patients with only index lesion(s) within 10% isodose line of prior treatment would be excluded. For example, if ALL index lesions are within the 2.2Gy isodose line of previously treated lesions to 22Gy in 1 fractions, the patient would be ineligible, however if there is 1 index lesion not in the prior radiation field, then that patient would be eligible but all other lesions in prior radiation fields would be excluded from analysis. 6. Inability to tolerate 18F-fluciclovine PET/CT exam 7. Enrollment delays patient care 8. Concurrent or prior enrollment on other clinical trials would not exclude patients, as long as all other eligibility criteria are met.
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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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Arizona Cancer Center at UMC North/University Medical Center
RECRUITINGTucson, Arizona, 85719, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can doctors watch brain metastases instead of zapping them?
- Starving brain tumors of blood before surgery
- Tiny gadolinium particles aim to make brain radiation hit harder
- A sharper MRI could reveal radiation sensitivity of brain tumors
- Expert tumor board may extend survival in brain metastases
- Can a new pill outsmart lung cancer in the brain?