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CompletedPhase 3

Clinical use of [18F]florastamine PET/CT in patients with PI-RADS≤3 report of multi-parametric MRI and suspected prostate cancer

EU 2023-510421-14-00 · Run by Curium Austria GmbH · Record updated 12 August 2024

Where in Austria

  • Klagenfurt Am Woerthersee · Landeskrankenanstalten-Betriebsgesellschaft KabegCompleted
  • Salzburg · Gemeinnuetzige Salzburger Landeskliniken Betriebsgesellschaft mbHCompleted
The registry text, word for word

Prospective Study of Added Value of Florastamin (18F) PET/CT in Localisation of Clinically Significant Prostate Cancer in Patients with PI- Report of Multi-Parametric MRI, Elevated Serum PSA Levels and/or PSA Density and with Clinical Suspicion of Prostate Cancer

To analyse the sensitivity of florastamin (18F) PET/CT in localisation of csPCa in patients with elevated serum PSA levels and/or PSA density and with clinical suspicion of PCa and with report of PI-RADS v2.1.

Inclusion: Male gender; Age ≥18 years; PSA ≥10ng/mL and/or PSAD≥0.26 ng/mL2; PI-RADS v2 ≤3 report of mpMRI performed less than 3 months prior inclusion; Availability of mpMRI data for centralized reading; Patient scheduled for biopsy or radical prostatectomy; Signed informed consent.

Exclusion: Androgen deprivation therapy or any targeted treatment for PCa prior florastamin (18F) PET/CT; Concomitant active malignancy and/or confirmed metastases; Hypersensitivity to active substance or any of excipients of investigational medicinal product; Past history of confirmed prostate cancer; Absence of any of the inclusion criteria; Life expectancy <6 months; ECOG performance status >2.

EU CTIS 2023-510421-14-00