NCT07735819Not yet recruitingPhase 2
Positron Emission Tomography/Computed Tomography (PET/CT) Imaging in Patients Diagnosed With a Glioma
Tryptophan-kynurenine Pathway PET Imaging in Human Gliomas
Source: ClinicalTrials.gov · Last updated 30 Jul 2026
Brief summary (registry, in English)
The goal of this clinical trial is to evaluate Positron emission tomography/computed tomography (PET/CT) imaging with the radiotracer 1-(2-\[18F\]fluoroethyl)-l-tryptophan (\[18F\]FETrp) in patients diagnosed with a glioma. This study has 3 aims: * to assess if the \[18F\]FETrp PET/CT can outperform Magnetic Resonance Imaging (MRI) by providing a better treatment target volume in newly diagnosed Stage 4 glioma patients * better differentiate tumor progression from radiation induced MRI changes in post treatment stage 4 gliomas * by giving a drug that can inhibit a pathway to allow objective assessment of treatment effects in low grade gliomas
- Status (registry)
- Not yet recruiting
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 61 (estimated)
- First submitted
- 24 Jul 2026
- Start date
- Sept 2026
- Primary completion date
- 30 Jun 2031
- Lead sponsor
- Barbara Ann Karmanos Cancer Institute
- Diseases
- Glioblastoma
- NCT number
- NCT07735819
What you commit to
- Study type: Interventional · Phase 2
- Planned participants: 61
- From Sept 2026 to the primary completion date, 30 Jun 2031
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Active connective tissue disorders, such as lupus or scleroderma.
- History of allergic reaction to minocycline or any tetracyclines.
- History of colitis during antibiotics treatment.
Lab values
- Patients who are pregnant or lactating are excluded. Premenopausal women (defined per institutional guidelines) must have a negative pregnancy test (urine or serum) within 7 days of the PET scan.
- Ongoing treatment with warfarin with INR \> 1.5.
Other
- Severe increased intracranial pressure, status epilepticus, or other severe or progressing clinical symptoms requiring urgent intervention in the opinion of the treating
- Karnofsky performance score \<60, as determined by one of the clinician co- investigators.
- ADDITIONAL CRITERIA FOR ARM 1:
Who the study is looking for
- Age =18 years.
- Patient is able to lie in the PET/CT scanner for at least 60 minutes while undergoing scanning.
- Patient is willing and able to review, understand, and provide written consent for the study procedures and indicates that they are aware of the investigational nature of this study.
- Histopathology/cytopathological diagnosis of a glioblastoma without a history of radiation.
- The tumor is deemed amenable for radiation treatment (pre-radiation planning MRI can be done before or after the PET scan).
- ADDITIONAL CRITERIA FOR ARM 2:
- Previous histopathology/cytopathological diagnosis of glioblastoma.
- History of glioma radiation.
- Presence of a new or progressing enhancing brain lesion on follow-up clinical MRI suspicious for post-radiation glioma progression or late radiation-induced MRI changes (i.e., radiation injury), at least 7 mm in bidirectional diameter.
- The most recent MRI, used for comparison with the PET/CT, is performed within 4 weeks of the planned PET scan.
- ADDITIONAL CRITERIA FOR ARM 3
- MRI diagnosis of a brain tumor, previously verified to be a low-grade (WHO grade 2, IDH (isocitrate dehydrogenase) mutant glioma, based on histopathology from biopsy or resection.
- The detected mass on the most recent clinical MRI is at least 7 mm in bidirectional diameter (i.e., twice the PET scanner resolution).
- The tumor does not require urgent (within 1 month) resection, steroid treatment, or radiation.
- The most recent MRI, used for comparison with the PET/CT, is performed within 4 weeks.
- Patient agrees to have a baseline and follow-up PET/CT scan (approximately 1 month later) and interval oral treatment with 200mg/day minocycline.
- Due to planned minocycline treatment, patients will need to have adequate renal function
Criteria the registry did not label
- FOR ARMS 1-3
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Karmanos Cancer Institute Coordinator of this site? Confirm its status | Detroit | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.