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Recruiting NCT06335914

NCT06335914 Dual PSMA and FDG PET Imaging for Patients With Advanced Prostate Cancer

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Clinical Trial Summary
NCT ID NCT06335914
Status Recruiting
Phase
Sponsor University Health Network, Toronto
Condition Advanced Prostate Cancer
Study Type INTERVENTIONAL
Enrollment 30 participants
Start Date 2025-04-03
Primary Completion 2029-03-04

Eligibility & Interventions

Sex Male only
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Ga 68 PSMA-11 PET18F-DCFPyL PETFDG PET

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 30 participants in total. It began in 2025-04-03 with a primary completion date of 2029-03-04.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This study will use Prostate Specific Membrane Antigen (PSMA) and (18)F-Fluorodeoxyglucose Positron Emission Tomography (FDG PET) imaging in patients with advanced prostate cancer to learn about tumor biology across disease stages and during treatment. This may help with treatment selection and potential response monitoring in the future.

Eligibility Criteria

Inclusion Criteria: * Male, age ≥ 18 years * Histologically or cytologically confirmed prostate cancer (adenocarcinoma) * Poor risk patients with mCSPC at study enrollment * De novo or recurrent high volume mCSPC as per conventional imaging (CT chest abdomen pelvis, or MRI, plus bone scan) prior to starting ADT and ARPI * High or low volume mCSPC plus PSA ≥4.0 after 6-8 months of initiating ADT * Willing to undergo study PET scans and remain under the care of medical oncology, radiation oncology or urology physician at Princess Margaret Cancer Center. * No prior PSMA or FDG PET imaging within the last 60 days at each specified time point on study * Patients enrolled in clinical trials are eligible if they satisfy all other criteria of eligibility Exclusion Criteria: * Under a randomized-controlled trial with unknown allocation of systemic therapy * Inability to undergo or successfully complete PSMA PET and FDG PET imaging exams * Unable to provide written consent by patient and their legal representatives * In the opinion of the treating physician: * conditions which would significantly impair the patient's ability to comply with study procedures and follow up * Significant uncontrolled comorbidity, which may negatively impact the safety or interpretability of study PET imaging * another active malignancy * patient on dialysis * another radioisotope or investigational systemic agent within 5 half-lives prior to PET imaging

Contact & Investigator

Central Contact

Di (Maria) Jiang, M.D.

✉ di.jiang@uhn.ca

📞 416-946-4501

Principal Investigator

Di (Maria) Jiang

PRINCIPAL INVESTIGATOR

Princess Margaret Cancer Centre/University Health Network

Frequently Asked Questions

Who can join the NCT06335914 clinical trial?

This trial is open to male participants only, aged 18 Years or older, studying Advanced Prostate Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06335914 currently recruiting?

Yes, NCT06335914 is actively recruiting participants. Contact the research team at di.jiang@uhn.ca for enrollment information.

Where is the NCT06335914 trial being conducted?

This trial is being conducted at Toronto, Canada.

Who is sponsoring the NCT06335914 clinical trial?

NCT06335914 is sponsored by University Health Network, Toronto. The principal investigator is Di (Maria) Jiang at Princess Margaret Cancer Centre/University Health Network. The trial plans to enroll 30 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology