Actively Recruiting

Age: 18Years +
All Genders
NCT04935853

Prognostic and Predictive Markers of Response to Treatment in Patients With Bile Duct Cancer: ACABi PRONOBIL Study

Led by GERCOR - Multidisciplinary Oncology Cooperative Group · Updated on 2025-07-23

1350

Participants Needed

32

Research Sites

940 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The objective of this study is to identify prognosis and predictive markers of response to treatments (surgery, chemotherapy, targeted therapy,loco-regional treatments ) in patients with bile duct cancer. The effectiveness and tolerance of these treatments in current practice will also be evaluated.

CONDITIONS

Official Title

Prognostic and Predictive Markers of Response to Treatment in Patients With Bile Duct Cancer: ACABi PRONOBIL Study

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • All primary locations including intrahepatic cholangiocarcinoma, extrahepatic cholangiocarcinoma, and gallbladder adenocarcinoma (ampullomas excluded)
  • Aged over 18 years
  • Diagnosed with bile duct cancer between 2003 and 2030 with at least 2 years of follow-up
  • Provided written non-opposition or signed informed consent for genetic studies
  • Inclusion allowed in a therapeutic research protocol
Not Eligible

You will not qualify if you...

  • Under legal guardianship, curatorship, or legal protection
  • Pregnant or breastfeeding women
  • Any medical, psychological, or social condition that might prevent following the study protocol
  • Refusal to participate in the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 32 locations

1

CHU Hôpital Sud Amiens

Amiens, France

Actively Recruiting

2

CHU Angers

Angers, France

Actively Recruiting

3

CHU Besançon

Besançon, France

Actively Recruiting

4

Hôpital Avicenne

Bobigny, France

Actively Recruiting

5

CHU - Henri Mondor

Créteil, France

Actively Recruiting

6

CHU Dijon

Dijon, France

Actively Recruiting

7

CHU Grenoble

Grenoble, France

Actively Recruiting

8

CHU Lille

Lille, France

Actively Recruiting

9

Centre Léon Bérard

Lyon, France

Actively Recruiting

10

Hôpital Croix Rousse

Lyon, France

Actively Recruiting

11

Hôpital Edouard Herriot

Lyon, France

Actively Recruiting

12

Hôpital Privé Jean Mermoz

Lyon, France

Actively Recruiting

13

Institut Paoli Calmette

Marseille, France

Actively Recruiting

14

CHU Saint Eloi Montpellier

Montpellier, France

Actively Recruiting

15

CHR Orléans

Orléans, France

Actively Recruiting

16

Groupe Hospitalier Pitié Salpêtrière

Paris, France

Actively Recruiting

17

Hôpital Ambroise Paré

Paris, France

Actively Recruiting

18

Hôpital Cochin

Paris, France

Actively Recruiting

19

Hôpital Saint Antoine

Paris, France

Actively Recruiting

20

Hôpital Saint Louis

Paris, France

Actively Recruiting

21

Institut Mutualiste Montsouris

Paris, France

Actively Recruiting

22

Hôpital Haut Lévêque

Pessac, France

Actively Recruiting

23

CHU Poitiers

Potiers, France

Actively Recruiting

24

Hôpital Robert Debré -CHU Reims

Reims, France

Actively Recruiting

25

Centre Eugène Marquis

Rennes, France

Actively Recruiting

26

CHU Rouen Charles Nicolle

Rouen, France

Actively Recruiting

27

Institut Curie

Saint-Cloud, France

Actively Recruiting

28

CHU Saint Etienne

Saint-Etienne, France

Actively Recruiting

29

CHU Rangueil

Toulouse, France

Actively Recruiting

30

CHU Tours

Tours, France

Actively Recruiting

31

CHRU Nancy Site Brabois

Vandœuvre-lès-Nancy, France

Actively Recruiting

32

Institut Gustave Roussy

Villejuif, France

Actively Recruiting

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Research Team

C

Cindy Neuzillet, Dr

CONTACT

M

Marie-Line Garcia, Dr

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

0

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