Utility of 18F-rhPSMA-7.3 in the Diagnosis of Prostate Cancer After Focal Gland Treatment
Part of paid clinical trials in Hackensack, New Jersey.
- Sponsor
- Hackensack Meridian Health
- Study ID
- NCT07011342
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- MALE
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- 18F-rhPSMA-7.3 — DRUGUtility of 18F-rhPSMA-7.3 in the diagnosis of prostate cancer after Focal Gland Treatment (SCOUT)
Study Details
To evaluate the effectiveness of a PSMA-PET scan in identifying recurrent prostate cancer after focal therapy
Key Dates
- Start date
- Oct 1, 2025
- Status verified
- Mar 2026
- Primary completion
- Nov 30, 2028
- Completion
- Nov 30, 2028
Study Design
- Enrollment
- 70 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- DIAGNOSTIC
Arms
- Experimental: 18F-rhPSMA-7.3Patients will undergo a PSMA-PET scan at 1 year (+/- 60 days) after treatment with SOC focal therapy using a radiohybrid Prostate-Specific Membrane Antigen (rhPSMA)-targeted PET scan using 18F-rhPSMA-7.3 (Posluma). The rhPSMA-targeted PET scan is an FDA-approved PET scan to detect the presence of lesions positive for prostate-specific membrane antigen (PSMA) in men with prostate cancer. 18F-rhPSMA-7.3 (Posluma) injection is a radioactive diagnostic agent that is administered in the form of an intravenous injection.
Primary Outcome Measure
To evaluate the effectiveness of PSMA-PET scan in identifying recurrent prostate cancer after focal therapy [ Time Frame: Approximately 1 year after SOC focal therapy. ]
Central Contacts
- Oncology Clinical Research Referral Office551-996-1777
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| John Theurer Cancer Center at Hackensack University Medical Center | Hackensack | New Jersey | 07601 |
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