E.1 Medical condition or disease under investigation |
E.1.1 | Medical condition(s) being investigated |
de novo patients with histologically confirmed prostate cancer |
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MedDRA Classification |
E.1.2 Medical condition or disease under investigation |
E.1.2 | Version | 12.0 |
E.1.2 | Level | LLT |
E.1.2 | Classification code | 10060862 |
E.1.2 | Term | Prostate cancer |
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E.1.3 | Condition being studied is a rare disease | No |
E.2 Objective of the trial |
E.2.1 | Main objective of the trial |
Sensitivity and specificity of [18F]-FCH PET/CT for systemic disease (i.e., lymph node metastases and/or organ metastases and/or bone metastases) on a body region basis. |
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E.2.2 | Secondary objectives of the trial |
• Sensitivity and specificity of [18F]-FCH PET/CT for lymph node metastases using histopathology as the SOR and CT as a comparator (per lymph node area; only lymph nodes area with histopathological analysis). Quantification using SUV (quantitative uptake in lymph nodes) will be used. • Agreement rate between [18F]-FCH PET/CT and CT for organ metastases on a region basis. Discrepant cases will be documented by MRI (except for lung metastases). For lung metastases, discrepant results will be documented by a chest CT performed within 6 monthsafter [18F]-FCH PET/CT. • Agreement rate between [18F]-FCH PET/CT and bone scintigraphy with regard to bone metastases (on a body region basis). Discrepant cases will be documented by MRI. • Sensitivity and specificity of [18F]-FCH PET/CT for systemic disease (i.e., lymph node metastases and/or organ metastases and/or bone metastases) on a patient basis. • Modification of tumor primary staging and patient management. • Safety of [18F]-FCH
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E.2.3 | Trial contains a sub-study | No |
E.3 | Principal inclusion criteria |
1. Male 2. Age > or = 18 years 3. De novo patient with histologically confirmed prostate cancer and high risk disease according to D’AMICO criteria: stages > or = T2c and/or PSA > or = 20 ng/ml and/or Gleason score > or = 8, or Gleason score = 7 with either predominance of grade 4 or percentage of positive biopsy > 50% 4. Patient who has already been imaged by contrast-enhanced thoraco-abdominal CT and bone scintigraphy 5. Patient who is able to undergo all study procedures and who has signed a written informed consent form to participate in the study
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E.4 | Principal exclusion criteria |
1. Surgery within the last 4 weeks prior to the administration of [18F]-FCH 2. History of other malignant tumor 3. Previous radiation therapy 4. Prostate biopsy within 4 weeks before [18F]-FCH PET/CT 5. Concomitant medications containing choline 6. Severe allergic reaction to any of the ingredients of the choline formulation 7. Participation in another clinical study within one month prior to inclusion 8. Uncooperative, in the investigator's opinion 9. Linguistic or psychological inability to sign the informed consent form and/or take part in the study 10. Having already participated in this clinical trial
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E.5 End points |
E.5.1 | Primary end point(s) |
Sensitivity and specificity of [18F]-FCH PET/CT for primary staging of prostate cancer |
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E.6 and E.7 Scope of the trial |
E.6 | Scope of the trial |
E.6.1 | Diagnosis | Yes |
E.6.2 | Prophylaxis | No |
E.6.3 | Therapy | No |
E.6.4 | Safety | Yes |
E.6.5 | Efficacy | Yes |
E.6.6 | Pharmacokinetic | No |
E.6.7 | Pharmacodynamic | No |
E.6.8 | Bioequivalence | No |
E.6.9 | Dose response | No |
E.6.10 | Pharmacogenetic | No |
E.6.11 | Pharmacogenomic | No |
E.6.12 | Pharmacoeconomic | No |
E.6.13 | Others | No |
E.7 | Trial type and phase |
E.7.1 | Human pharmacology (Phase I) | No |
E.7.1.1 | First administration to humans | No |
E.7.1.2 | Bioequivalence study | No |
E.7.1.3 | Other | No |
E.7.1.3.1 | Other trial type description | |
E.7.2 | Therapeutic exploratory (Phase II) | No |
E.7.3 | Therapeutic confirmatory (Phase III) | Yes |
E.7.4 | Therapeutic use (Phase IV) | No |
E.8 Design of the trial |
E.8.1 | Controlled | Yes |
E.8.1.1 | Randomised | No |
E.8.1.2 | Open | Yes |
E.8.1.3 | Single blind | No |
E.8.1.4 | Double blind | No |
E.8.1.5 | Parallel group | No |
E.8.1.6 | Cross over | No |
E.8.1.7 | Other | Yes |
E.8.1.7.1 | Other trial design description |
Blinded read session of the imaging results |
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E.8.2 | Comparator of controlled trial |
E.8.2.1 | Other medicinal product(s) | No |
E.8.2.2 | Placebo | No |
E.8.2.3 | Other | Yes |
E.8.2.3.1 | Comparator description |
CT scan and bone scintigraphy. |
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E.8.3 |
The trial involves single site in the Member State concerned
| Yes |
E.8.4 | The trial involves multiple sites in the Member State concerned | No |
E.8.5 | The trial involves multiple Member States | No |
E.8.6 Trial involving sites outside the EEA |
E.8.6.1 | Trial being conducted both within and outside the EEA | No |
E.8.6.2 | Trial being conducted completely outside of the EEA | Information not present in EudraCT |
E.8.7 | Trial has a data monitoring committee | No |
E.8.8 |
Definition of the end of the trial and justification where it is not the last
visit of the last subject undergoing the trial
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The end of the trial will take place when the last patient undergoing the trial will have finished the follow up period. The follow up period may contain additional imaging tests (MRI or chest CT) which have to be done within 6 months after injection of the study product. The additional imaging tests concern patients with discrepant results between [18F]-FCH and CT or bone scintigraphy. |
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E.8.9 Initial estimate of the duration of the trial |
E.8.9.1 | In the Member State concerned years | 1 |
E.8.9.1 | In the Member State concerned months | 3 |
E.8.9.1 | In the Member State concerned days | 0 |
E.8.9.2 | In all countries concerned by the trial years | 0 |
E.8.9.2 | In all countries concerned by the trial months | 0 |
E.8.9.2 | In all countries concerned by the trial days | 0 |