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High Grade GliomaEarly Phase 1NCT05632562

Multiparametic Metabolic and Hypoxic PET/MRI for Disease Assessment in High Grade Glioma

A Early Phase 1 study testing O-(2-[18F]Fluoroethyl)-L-tyrosine, [18F]-FET with PET/MRI in people with High Grade Glioma, run by University of Alabama at Birmingham at 2 sites in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This feasibility study will assess the clinical potential of a new imaging approach to detect viable high grade glioma (HGG) in pediatric and adult patients after standard of care radiation therapy (RT) with or without concurrent temozolomide (TMZ). Read more about this study

Who is it for?
Ages 10 to 89 years
Conditions the study is for
High Grade Glioma
What is being tested?
O-(2-[18F]Fluoroethyl)-L-tyrosine, [18F]-FET with PET/MRI
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
20 participants
Where
2 sitesUnited States
Study dates
7 Mar 2024to 1 Feb 2028
Phase
Early Phase 1
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 10 to 89 years
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

  • Histologically confirmed newly diagnosed grade III or grade IV glioma treated with standard of care external beam radiation therapy (RT). For diffuse midline glioma involving the pons (diffuse intrinsic pontine glioma), histological confirmation is not required. Surgical resection of the glioma prior to RT and/or concurrent temozolomide (TMZ) with RT are allowed but not required.
  • 10 years of age or older at the time of enrollment
  • Able to undergo PET/MRI without anesthesia or sedation. Minimal sedation with an anxiolytic such as alprazolam used routinely for SOC MRI is allowed.
  • Females with childbearing potential must have a negative urine β-hCG test on the day of procedure or a serum beta-hCG test within 48 hours prior to the administration of FET or FMISO.
  • ECOG performance score of 2 or better in adults. For patients less than 16 years of age, Modified Lansky score ≥ 60.
  • Life expectancy greater than 12 weeks.

Who cannot join

  • Recurrent glioma
  • Use of bevacizumab or an investigational therapeutic drug for any indication within 3 months prior to the imaging study.
  • Pregnancy or breast feeding
  • Inability to complete PET/MRI scans.
  • Significant renal dysfunction (estimated GFR < 30 mL/min)
  • Any condition which may interfere with ability to participate in or complete all study-related activities as assessed by the study team
  • Time interval greater than 12 weeks between the completion of RT and performance of FET and FMISO PET/MRI studies.

Trial locations and contacts

2 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Sebastian M Eady, BS contact

205-996-2636

smeady@uabmc.edu

Quenteeria S Mooney, BS contact

205-934-3747

qmooney@uabmc.edu

United States2 sites, 2 recruiting
  • UAB

    Birmingham, Alabama, 35249

    Not yet recruiting
  • UAB

    Birmingham, Alabama, 35249

    Sebastian Eady, 205-966-2636, smeady@uabmc.edu

    Recruiting

Other trials in United States

About this study

This feasibility study will assess the clinical potential of a new imaging approach to detect viable high grade glioma (HGG) in pediatric and adult patients after standard of care radiation therapy (RT) with or without concurrent temozolomide (TMZ). Study participants will undergo simultaneous positron emission tomography/magnetic resonance imaging (PET/MRI) with O-([2-[F-18]fluoroethyl)-L-tyrosine (FET, amino acid transport) and 1H-1-(3-[F-18]fluoro-2-hydroxypropyl)-2-nitroimidazole (FMISO, hypoxia) at the time of standard of care imaging after completion of RT. The presence of viable tumor at this time point will be assessed on a per patient basis. Study participants will be followed clinically and with standard of care (SOC) imaging for up to 2 years after completion of PET/MRI to determine the nature of lesions seen on investigational imaging and to obtain patient outcome data. The imaging data will also be used to develop a semi-automated workflow suitable for implementation in clinical trials and standard of care PET/MRI studies.

Read the detailed description

Patient recruitment

Potential participants will be identified through the UAB and Children's of Alabama (CoA) Neuro-Oncology, Neurosurgery and Radiation Oncology services. Patients seen in UAB clinics and/or discussed in multi-disciplinary neuro-oncology tumor board meetings may be approached to participate in this study. Potential participants can be enrolled from the time that the plan for standard of care therapy is selected through the time of the first standard of care of MRI after radiation therapy. Given that high grade gliomas are much more frequent in adults than children, we expect to recruit mostly adults in this study.

Confirmation of patient eligibility

The following information will be collected to confirm patient eligibility prior to the administration of FET.

  1. Registering physician's name.
  2. Participant's sex, race and date of birth.
  3. Copy of signed consent form
  4. Completed eligibility checklist that has been signed and dated by a member of the study team.
  5. Copy of source documentation confirming patient eligibility.

Initial Visit

Potential participants will meet with study personnel in the appropriate neuro-oncology clinic or on the 7th floor of Jefferson Tower/Quarterback Tower. For pediatric patients under the age of consent, a parent or legal guardian will provide consent, and when possible and age appropriate, the child will provide assent. Questions will be answered, and once the participant signs informed consent, blood will be drawn to measure serum creatinine and calculate estimated GFR (eGFR). In pediatric patients, this blood draw will also be used to measure cystatin C for use in eGFR calculation. Serum creatinine and cystatin C measurements will not be required if results from previous tests within the past 4 weeks are available and meet eligibility requirements. For women with childbearing potential, a serum beta-hCG pregnancy test will be drawn along with the serum creatinine blood draw; a urine pregnancy test is acceptable to avoid a blood draw if no serum creatinine measurement is needed.

PET/MRI visits

After confirmation of patient eligibility and consent, the administration of FET and FMISO and related procedures will be performed in the UAB Advanced Imaging Facility (AIF) at the time of first SOC MRI after completion of RT (typically a 4-week interval). FET and FMISO PET/MRI studies will be performed on separate days within 2 weeks of each other, and every effort will be made to perform these studies within 1 week of each other. FET-PET/MRI will typically be performed before FMISO-PET/MRI although the order can be switched if needed from due to PET tracer production or scanner scheduling. Patients will fast for at least 4 hours prior to FET administration. No fasting or other special preparation is required for FMISO studies. Upon arrival in the AIF, the patient (and their legal medical decision maker if needed) will have an opportunity to have any remaining questions answered regarding the procedure.

The participant will have a plastic peripheral intravenous (IV) catheter placed in the arm for PET tracer and MR contrast administration. FET and FMISO will be produced by the UAB Cyclotron PET Production Facility. PET/MRI will be performed using a GE Signa PET/MRI system in the AIF with specific imaging protocols for FET and FMISO studies. Upon completion of imaging, the peripheral IV catheter will be removed. The participant will be asked to urinate to reduce bladder dose after completion of each PET acquisition. The PET data will be reconstructed using OSEM algorithms with correction for radionuclide decay, randoms and scatter according to the manufacturer's standard procedure. Attenuation correction will be performed using standard MR-based attenuation correction according to the manufacturer's recommendations.

If the PET/MRI is unexpectedly unavailable, participants can undergo brain PET imaging on a GE 710 PET/CT scanner located adjacent to the PET/MRI scanner in the AIF. The PET tracer administration and PET acquisition will be identical to the protocol described previously for PET/MRI. Attenuation correction of the PET data will be based on a low dose head CT (120 kVp, 30 mAs) for the PET/CT study. Participants undergoing PET/CT will have a separately acquired MRI study using the same MRI sequences described previously for the PET/MRI study.

FET-PET/MRI protocol

The patient will be positioned in the PET/MRI scanner prior to FET administration. FET (5 mCi, 185 MBq) will be administered IV as a bolus with dynamic acquisition of brain PET/MRI data from the time of injection through 60 min after injection. The dynamic FET-PET data will be framed according to the following schedule: 12 x 5 sec, 12 x 10 sec, 6 x 20 sec, 15 x 60 sec, and 5 min for the remainder of the study. The raw PET data will be retained for possible future reprocessing.

During FET-PET acquisition, brain MRI will be acquired simultaneously. Multiplanar, multisequence contrast-enhanced MR images will be acquired based on the standard of care adult brain tumor imaging protocol at UAB and will include dynamic contrast enhanced (DCE) and diffusion weighted (DW) sequences as well as a 3D post-contrast T1 sequence to calculate contrast enhancing volumes and 3D FLAIR sequence to calculate non-enhancing peritumoral volumes.

FMISO-PET/MRI protocol

The patient will undergo IV administration of FMISO (5 mCi, 185 MBq) in an uptake room in the AIF. At approximately 4 hours after injection, the patient will be positioned on the PET/MRI scanner. A PET scan will be acquired for 30 min, and simultaneous contrast-enhanced MRI will be acquired which may include repeat DCE and DW sequences.

Participant Follow-up

The patients and/or their legally authorized representative will be asked about any adverse events at the conclusion of each PET scan. They will also be contacted by telephone 24-48 hours after PET tracer administration to confirm that the participant is in their usual state of health and to assess for any adverse events related to the imaging study. No additional follow up to assess for adverse events will be performed unless a possible study-related adverse event is reported.

Duration of Follow Up:

Patients enrolled in the study will be followed clinically and with standard of care brain MRI. PFS and OS will be monitored for up to 24 months after completion of FET and FMISO PET/MRI studies. Relevant medical information may be accessed by study team members for correlation with imaging results including clinic notes, diagnostic imaging, histopathology and genetic tumor markers relevant to HGG classification and prognosis (e.g. MGMT promotor methylation, IDH mutation status). Study participants will not undergo additional study related procedures after completion of the FET-PET/MRI and FMISO-PET/MRI studies.

Being tested
O-(2-[18F]Fluoroethyl)-L-tyrosine, [18F]-FET with PET/MRI
Medical subject headings
Glioma

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • O-(2-[18F]Fluoroethyl)-L-tyrosine, [18F]-FET with PET/MRIDrug

    High grade glioma patients that are planning to undergo radiation therapy (RT) and consent to this study will have up to 3 in-person study visits. The first visit will take up to 2 hours, the second visit will take up to 3 hours, and the third visit will take up to 6 hours. After both imaging visits, there will be a phone call at 24-48 hours after imaging.After confirmation of patient eligibility and consent, the administration of FET and FMISO and related procedures will be performed in the UAB Advanced Imaging Facility (AIF) at the time of first standard of care (SOC) MRI after completion of RT (typically a 4-week interval). Patients enrolled in the study will be followed clinically and with standard of care brain MRI. PFS and OS will be monitored for up to 24 months after completion of FET and FMISO PET/MRI studies. Study participants will not undergo additional study related procedures after completion of the FET-PET/MRI and FMISO-PET/MRI studies.

Study groups in NCT05632562
Study groupRoleWhat they receive
PET imaging of system L amino acid transport with FET and hypoxia imaging with FMISOExperimentalThe participant will have a plastic peripheral intravenous (IV) catheter placed in the arm for Positron emission tomography (PET) tracer and MR contrast administration. FET O-([2-[18F]fluoroethyl)-L-tyrosine and FMISO 1H-1-(3-[18F]fluoro-2-hydroxypropyl)-2-nitroimidazole will be produced by the UAB Cyclotron PET Production Facility. PET/MRI will be performed using a GE Signa PET/MRI system in the AIF with specific imaging protocols for FET and FMISO studies. Upon completion of imaging, the peripheral IV catheter will be removed. The participant will be asked to urinate to reduce bladder dose after completion of each PET acquisition.Patients enrolled in the study will be followed clinically and with standard of care brain MRI. PFS and OS will be monitored for up to 24 months after completion of FET and FMISO PET/MRI studies.
Receives: Drug: O-(2-[18F]Fluoroethyl)-L-tyrosine, [18F]-FET with PET/MRI

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Detection of viable glioma based on PET

    The frequency of the detection of viable tumor by FET and/or FMISO based on prespecified standardized uptake values (SUVs) and lesion to normal brain ratios will be measured. We expect to detect viable glioma in at least 25% of patients at this time point.

    Measured: Up to 24 months after completing study PET/MRI visits.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted30 Nov 2022
  2. Study start7 Mar 2024
  3. Primary completion1 Feb 2028 (estimated)
  4. Study completion1 Feb 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Early Phase 1
Primary purpose
Diagnosis
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
20 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05632562
Sponsor's protocol ID
IRB-300010076 R22-193
Other IDs
300010076
Status last verified
Aug 2026
First submitted
9 Nov 2022
Last updated
20 Aug 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A Early Phase 1 study testing O-(2-[18F]Fluoroethyl)-L-tyrosine, [18F]-FET with PET/MRI in people with High Grade Glioma, run by University of Alabama at Birmingham at 2 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 20 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Early Phase 1 (sometimes called Phase 0) studies give a very small amount of a treatment to a few people, mainly to see how the body handles it.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Sebastian M Eady, BS (205-996-2636, smeady@uabmc.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Detection of viable glioma based on PET (time frame: Up to 24 months after completing study PET/MRI visits.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Aug 2026.

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