Effectiveness of Posluma PET Scan for Post-Treatment Monitoring of Prostate Cancer
- Sponsor
- Aditya Bagrodia
- Study ID
- NCT07733908
- Phase
- PHASE2
- Status
- Not Yet Recruiting
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Conditions
Eligibility Criteria
- Sex
- MALE
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Posluma PET — DIAGNOSTIC_TESTPosluma® (flotufolastat F 18) is an FDA-approved diagnostic PET imaging agent used to detect prostate-specific membrane antigen (PSMA)-positive lesions in men with prostate cancer. It helps pinpoint the location of cancer when metastasis is suspected or when recurrence occurs due to elevated PSA levels.
Study Details
To determine the effectiveness of Posluma PET Scan for monitoring prostate cancer patients after targeted treatment, including how accurately it can detect any remaining or returning cancer after about 12 months post-treatment.
Key Dates
- First listed
- Jul 29, 2026
- Start date
- Aug 31, 2026
- Status verified
- Aug 2026
- Primary completion
- Jul 31, 2030
- Completion
- Jul 31, 2030
Study Design
- Enrollment
- 22 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SINGLE_GROUP
- Primary purpose
- SUPPORTIVE_CARE
Arms
- Experimental: Posluma PETParticipants will undergo Posluma PSMA PET scans at two time points: preoperatively to evaluate the extent of disease prior to focal therapy and postoperatively for monitoring treatment success and detecting potential recurrence. The Posluma PET imaging will be conducted on a PET/CT scanner with optimized protocols for PCa lesion detection. PET scan data will be analyzed in comparison with MRI and biopsy results. All imaging will be performed at UCSD, ensuring consistent imaging quality and scanner calibration across all patients.
Primary Outcome Measure
Diagnostic performance of Posluma PSMA PET scan for prostate cancer after focal therapy [ Time Frame: 12 months ]
Central Contacts
- Translational Research Team(858) 822-5354
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