Clinical trial · Interventional
[18F]PSMA-11 PET/CT Phase 3 Clinical Study
[18F]PSMA-11 PET/CT for Prostate Cancer - Phase 3 Clinical Study
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Prostate cancer (PCa) is the most frequently occurring male cancer in Belgium. After treatment with surgery and/or radiotherapy, almost half of the patients suffer from a tumor recurrence, often diagnosed by an increase in serum tumor marker Prostate Specific Antigen (PSA) within the first few years after primary treatment. However, for salvage therapy to be successful, precise localization of metastases is necessary to determine the most appropriate treatment. In so-called oligo-metastatic disease targeted therapy may still be curative and prevent the disease from spreading to distant locations. Therefore it is of paramount importance to have an accurate tool of medical imaging to localize all possible locations to be treated. Recently, prostate specific membrane antigen (PSMA) has gained interest for PCa-specific imaging. Due to overexpression of PSMA in both primary and metastatic PCa, radiotracers targeting this protein have shown an increased selectivity and sensitivity compared to conventional imaging. The main objective of this phase 3 trial is to determine the position of \[18F\]PSMA-11 PET/CT within the field of available radiotracers for diagnosis of prostate cancer. For this, the diagnostic performances of \[18F\]PSMA-11 will be compared to those of the current state-of-the-art radiotracer \[68Ga\]PSMA-11.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Prostate Cancer | Malignant Prostate Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| [18F]PSMA-11 | Diagnostic Test | — | UNRESOLVED |
| [68Ga]PSMA-11 | Diagnostic Test | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- PET/CT 1: [18F]PSMA-11, PET/CT 2: [68Ga]PSMA-11
- description
- Patients in this arm will first receive the experimental radiotracer \[18F\]PSMA-11 PET/CT followed by the \[68Ga\]PSMA-11 PET/CT after at least 4 days and maximum 3 weeks.
- interventionNames
- Diagnostic Test: [18F]PSMA-11
- Diagnostic Test: [68Ga]PSMA-11
- type
- ACTIVE_COMPARATOR
- label
- PET/CT 1: [68Ga]PSMA-11, PET/CT 2: [18F]PSMA-11
- description
- Patients in this arm will first receive the experimental radiotracer \[68Ga\]PSMA-11 PET/CT followed by the \[18F\]PSMA-11 PET/CT after at least 4 days and maximum 3 weeks.
- interventionNames
- Diagnostic Test: [18F]PSMA-11
- Diagnostic Test: [68Ga]PSMA-11
Primary outcomes (1)
Eligibility
Eligibility (as posted)
- Sex
- Male
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Patients diagnosed with prostate cancer, either in the setting of diagnosis of biochemical recurrence after previous treatment, or at primary diagnosis and staging. Exclusion Criteria: * Age \< 18 years * Physically or mentally unfit to perform the sequential procedures * Refusal of patient to be informed about accidental findings on scans * History of anaphylactic shock after administration of Visipaque CT contrast * Serum creatinine concentration \> 2.0 mg/dl and/or estimated glomerular filtration rate \< 60 ml/min.
References
Publications (0)
Data not yet available