Study of Diagnostic Performance of [18F]CTT1057 for PSMA-positive Tumors Detection

Inclusion Criteria:

Untreated high risk biopsy-proven PCa patients according to D'Amico classification (Stage ≥ T2c or PSA level >20ng/ml or Gleason score ≥8) (D'Amico et al 1998)
Scheduled or planned radical prostatectomy and extended pelvic lymph node resection up to 6 weeks after the investigational PET/CT scan followed by histopathology assessment
ECOG performance status 0-2
Signed informed consent must be obtained prior to participation in the study
Participants must be adults ≥ 18 years of age

Exclusion Criteria:

Inability to complete the needed investigational and standard-of-care imaging examinations due to any reason (severe claustrophobia, inability to lie still for the entire imaging time, etc.)
Any additional medical condition, serious intercurrent illness, concomitant cancer or other extenuating circumstance that, in the opinion of the Investigator, would indicate a significant risk to safety or impair study participation, including, but not limited to, current severe urinary incontinence, hydronephrosis, severe voiding dysfunction, need of indwelling/condom catheters, New York Heart Association class III or IV congestive heart failure, history of congenital prolonged QT syndrome, uncontrolled infection, active hepatitis B or C, and COVID-19.
Known allergy, hypersensitivity, or intolerance to [18F]CTT1057
Prior and current use of PSMA targeted therapies
Prior and current treatment with any ADT (first or second generation), including LHRH analogues (agonists or antagonists)
Any 5-alpha reductase inhibitors within 30 days before screening
Patients with small cell or neuroendocrine PCa in more than 50% of biopsy tissue
Patients with incidental PCa after transurethral resection
Use of other investigational drugs within 30 days before screening