Sign in

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
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

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Institut Curie -site Saint-Cloud
Coordinator of this site? Confirm its status
Saint-CloudFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.