NCT06659705RecruitingPhase 2
Cutting Edge Imaging With PET-FAPI for Earlier Pancreatic Cancer Diagnosis (INDIGO-FAPI)
Cutting Edge Imaging for Earlier Pancreatic Cancer Diagnosis: Evaluation of Positron Emission Tomography (PET) With the Fibroblast Activation Protein Inhibitor (FAPI)
Source: ClinicalTrials.gov · Last updated 15 Apr 2026
Brief summary (registry, in English)
Assessment of the relevance of a new medical imaging test, FAPI PET, which could detect progression or relapse earlier than other tests currently available. Ultimately, it could enable early forms of pancreatic cancer to be detected and used for screening. In addition to the usual examinations prescribed, FAPI PET scans will be repeated at several points in the treatment process. All study patients must first have been included in the Homing cohort (NCT 04363983, APHP promotion). Clinical characteristics, judgement criteria and results of biological or imaging examinations carried out as part of this cohort will be shared. Patient follow-up and participation in the study ends when conventional imaging (CT and MRI) shows disease progression, relapse or death.
- Status (registry)
- Recruiting
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 35 (estimated)
- First submitted
- 21 Oct 2024
- Start date
- 2 Dec 2025
- Primary completion date
- 4 Aug 2029
- Lead sponsor
- Institut Curie
- Diseases
- Pancreatic cancer
- NCT number
- NCT06659705
What you commit to
- Study type: Interventional · Phase 2
- Planned participants: 35
- From 2 Dec 2025 to the primary completion date, 4 Aug 2029
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other
- Protected adults (guardianship, curatorship or safeguarding justice)
- Pregnant or breastfeeding woman
- Women of childbearing potential not using one highly effective method of contraception
Who the study is looking for
- Cyto/histologically proven PDAC
- Non-metastatic proven PDAC on recent (\< 1 month) CT-scan and MRI
- Concomitant enrollment in the HoMING prospective cohort (Sponsor: AP-HP, NCT04363983)
- Age \> 18 years old
- Affiliation to a social security scheme
- Signed informed consent
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Institut Curie -site Saint-Cloud Coordinator of this site? Confirm its status | Saint-Cloud | France | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.