RecruitingNot ApplicableNCT02534649

Bergonie Institut Profiling : Fighting Cancer by Matching Molecular Alterations and Drugs in Early Phase Trials


Sponsor

Institut Bergonié

Enrollment

10,000 participants

Start Date

Dec 1, 2015

Study Type

INTERVENTIONAL

Conditions

Summary

This is a biology driven, monocentric study designed to identify actionable molecular alterations in cancer patients with advanced disease. In this trial, high throughput analysis will be carried out using next generation sequencing, and immunological profiling. Patients included in the BIP study and for whom a targetable genomic alteration had been identified might be subsequently included in an early phase trials running at Institut Bergonie or another French hospital.


Eligibility

Min Age: 18 Years

Inclusion Criteria8

  • Age ≥ 18 years,
  • Histology: solid malignant tumor or hematological malignancy,
  • Deleted MSA9
  • Deleted MSA9,
  • Deleted MSA9,
  • Deleted MSA9,
  • Patient with a social security in compliance with the French law relating to biomedical research (Article L.1121-11 of French Public Health Code),
  • Voluntary signed and dated written informed consent prior to any study specific procedure.

Exclusion Criteria11

  • Deleted MSA9
  • Deleted MSA9
  • Deleted MSA9
  • Deleted MSA9
  • Deleted MSA9
  • Deleted MSA9
  • Deleted MSA9
  • Deleted MSA9
  • Individuals deprived of liberty or placed under guardianship
  • Pregnant or breast feeding women,
  • Previous enrolment in the present study.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

PROCEDURENewly obtained biopsy and Blood samples collection

For each patient: * Frozen and paraffin embedded tumor material (archival or new biopsy) will be obtained for genetic profiling * Four blood samples will be obtained for genetic profiling and assessment of markers The results of each tumor profile will be discussed within a multidisciplinary tumor board which aims at discussing the genomic profiles and at providing a therapeutic decision for each patient. Patients for whom no molecular aberration has been identified will be treated at the discretion of the investigator and followed until death or study termination whichever occurs first. All the patients carrying a molecular aberration will be proposed to enter in a clinical trial depending on the possibility of inclusion at the time of molecular report.


Locations(7)

Centre Hospitalier de la Côte Basque

Bayonne, France

Clinique Tivoli-Ducos

Bordeaux, France

Institut Bergonie

Bordeaux, France

Polyclinique Bordeaux Nord Aquitaine

Bordeaux, France

Centre Hospitalier de Pau

Pau, France

Clinique Marzet

Pau, France

Centre Eugène Marquis

Rennes, France

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT02534649


Related Trials