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Study details
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Diagnostic Utility of rhPSMA-7.3 (18F) PET/CT in Men With Prostate Cancer on Active Surveillance

Icahn School of Medicine at Mount Sinai
NCT IDNCT07285057ClinicalTrials.gov data as of Apr 2026
Phase

Phase 2

Target enrollment

120

Study length

about 1.3 years

Ages

18+

Sex

Male only

Locations

1 site in NY

What this study is about

Researchers are testing whether adding PSMA-based PET/CT to standard MRI improves the detection of clinically significant prostate cancer compared to MRI alone in men with low-risk or favorable intermediate-risk prostate cancer managed with active surveillance. The trial will assess how well the PET/CT scan matches up with the biopsy results and determine if it can help upgrade a diagnosis.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Receive rhPSMA-7.3 (18F) PET/CT Imaging (Flotufolastat F18, POSLUMA®)
  • 2.Take Flotufolastat F18

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

Diagnostic Agent (Positron Emitting Activity)

Endpoints

Secondary: Incremental detection rate of csPCa by PET/CT over MRI, Lesion-level concordance between rhPSMA-7.3 (¹⁸F) PET/CT, multiparametric MRI, and histopathology

Procedures

imaging

Body systems

Oncology