Actively Recruiting

Age: 18Years +
All Genders
NCT06705335

Convertases and Pancreatic Cancer: Cohort of Patients Treated for Pancreatic Adenocarcinoma

Led by Institut Bergonié · Updated on 2026-04-20

50

Participants Needed

1

Research Sites

144 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is a prospective, single-centre, observational study. The analysis of samples of pancreatic tumours and/or metastases taken during biopsy or surgery will lead to the determination of the level of expression of convertases in patients with pancreatic cancer and could be used as an additional prognostic means reinforcing those currently used.

CONDITIONS

Official Title

Convertases and Pancreatic Cancer: Cohort of Patients Treated for Pancreatic Adenocarcinoma

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Pancreatic adenocarcinoma suspected by imaging or confirmed by biopsy
  • Indication for biopsy of metastases or pancreatic surgery as part of standard care
  • Any disease stage
  • Any type of treatment planned (systemic, surgery, radiotherapy, etc.)
  • No prior systemic treatment or advanced radiotherapy
  • WHO performance status 0, 1, or 2
  • Life expectancy greater than 3 months
  • Signed free, informed written consent before any study-specific procedure
  • Affiliated with a social security scheme as required by French law
Not Eligible

You will not qualify if you...

  • Biopsy performed for primary diagnosis of pancreatic cancer
  • No indication for pancreatic cancer treatment
  • Completed adjuvant or neoadjuvant chemotherapy less than 6 months ago for recurrent disease
  • Previously included in this study
  • Geographical, social, or psychological factors preventing study follow-up and procedures

AI-Screening

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Trial Site Locations

Total: 1 location

1

Institut Bergonié, Comprehensive Cancer Center

Bordeaux, France

Actively Recruiting

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Research Team

S

Simon PERNOT, Dr

CONTACT

C

Caroline LALET

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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