← Back to Clinical Trials
Recruiting Phase 2, Phase 3 NCT07098598

NCT07098598 Pancreatic Cancer Diagnosis With FAPI-PET Imaging

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT07098598
Status Recruiting
Phase Phase 2, Phase 3
Sponsor Turku University Hospital
Condition Positron Emission Tomography
Study Type INTERVENTIONAL
Enrollment 100 participants
Start Date 2024-10-09
Primary Completion 2026-10

Trial Parameters

Condition Positron Emission Tomography
Sponsor Turku University Hospital
Study Type INTERVENTIONAL
Phase Phase 2, Phase 3
Enrollment 100
Sex ALL
Min Age 18 Years
Max Age 85 Years
Start Date 2024-10-09
Completion 2026-10
Interventions
PET/CT

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

Brief Summary

Staging pancreatic cancer (PC) presents a clinical challenge. Triphasic whole body CT is the primary imaging method in diagnosing, staging and during follow up. Conventional PET/CT with 18F-labelled fluorodeoxyglucose (18F-FDG) has its limitations and therefore has a secondary role in imaging pancreatic cancer patients. These conventional imaging methods are good in detecting primary tumors and distant metastasis but poor in detecting local lymph node metastasis. A new PET tracer, fibroblast activation protein inhibitor (FAPI), targets FAP, a protein overexpressed in cancer-associated fibroblasts. It presents a potential new PET imagining tool. The objective of this prospective diagnostic study is to evaluate the diagnostic efficacy of 18F-FAPI-74 PET/CT in patients with PC. The aim is to evaluate the sensitivity and specificity of 18F-FAPI-74 in detection of local lymph node metastasis and distant metastasis in patient level in patients with PC in primary staging and when suspected recurrence. 100 patients with PC are enrolled on whom PET/CT studies are performed with the novel 18F-FAPI-74 tracer. The data will be collected between 2024-2026.

Eligibility Criteria

Inclusion Criteria: * Suspected primary or recurrent pancreatic cancer * Subjects must be male or female aged 18-85 years. * WHO performance score 0-2. * Subjects must be able and willing to give written informed consent and to comply with the requirements of this study protocol. Exclusion Criteria: * Vulnerable study subjects such as described in Finnish law clinical studies (disabled, children, pregnant or breast-feeding women, prisoners) will not be included. * Study subject is not able to understand the purpose of the study. * Medical conditions prohibiting whole-body PET/CT imaging.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology