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SUSPENDED
NCT05422105

Diagnostic Performance of 18F-PSMA-1007 PET/CT in Suspected Prostate Cancer Patient

Sponsor: Primo Biotechnology Co., Ltd

View on ClinicalTrials.gov

Summary

The diagnostic tools for detecting patients with early prostate cancer are limited due to poor diagnostic performance. The positron emission tomography (PET) combination with the diagnostic radiopharmacy is a non-invasive tool to provide the molecular imaging of the whole body and offer more comprehensive physiological information and then can raise the diagnostic performance. Prostate-specific membrane antigen (PSMA)-targeting pharmaceuticals have been regarded as the most promising diagnostic tool to diagnose patients with prostate cancer. Currently, the 18F-PSMA-1007 as PSMA-targeting 18F-radiolabeled pharmaceuticals have developed and successfully used in patients with intermittent- and high-risk prostate cancer or recurrent prostate cancer. The study aims to understand the diagnostic performance of 18F-PSMA-1007 PET/CT in different-stage prostate cancer patients by initiating the first multicenter clinical trial of 18F-PSMA-1007 in Taiwan.

Official title: Multicenter Evaluation of Diagnostic Performance of [18F]FPSMA-1007 PET/CT in Patients With Suspected Prostate Cancer

Key Details

Gender

MALE

Age Range

20 Years - 100 Years

Study Type

OBSERVATIONAL

Enrollment

230

Start Date

2023-07-01

Completion Date

2026-12-31

Last Updated

2026-07-06

Healthy Volunteers

No

Interventions

DRUG

18F-PSMA-1007

18F-PSMA-1007 PET/CT

Locations (2)

Tungs'Taichung Metro Harbor Hospital

Taichung, Taiwan

Shin Kong Wu Ho-Su Memorial Hospital

Taipei, Taiwan