Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Biobank for bronchial cancer patients to support research

Official title: Development of a Prospective Monocentric Clinico-Biological Database for Bronchial Cancer

Run by Institut du Cancer de Montpellier - Val d'Aurelle · NCT07085429 · Data updated 2026-11-12

A biobank project will collect blood and tissue samples from adults with bronchial cancer to help researchers study biology and improve future treatments.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment750 (estimated)
SponsorInstitut du Cancer de Montpellier - Val d'Aurelle
Academic / other
Drugs / interventionsimmunotherapy
Locations1 site (Montpellier, France)
StatusRecruiting
StartedNovember 25, 2025
Main results expectedSeptember 2030
Study endsSeptember 2040
Registry record updatedNovember 6, 2026
Trial IDNCT07085429 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults over 18 with histologically or cytologically confirmed bronchial cancer who have not yet begun treatment for their current cancer and who can provide informed consent.

Probably not a fit

Patients who do not consent or who have conditions preventing follow-up or sample collection may not benefit from this resource.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This project creates a tissue and blood biobank from patients with bronchial carcinoma, including both small-cell and non-small-cell types, treated at a single center in Montpellier. Samples are collected with informed consent from treatment-naïve adults and stored to support analytical and epidemiological research as well as development of new therapies. It aims to deepen understanding of how histological and molecular differences influence prognosis and response to therapy. The study does not involve a therapeutic intervention beyond sample collection. It is designed to enable future clinical research and trial development by providing high-quality biological material linked to clinical data.

Why it matters

Potential benefit: If successful, the biobank could accelerate discovery of biomarkers and guide future personalized treatment strategies for bronchial cancer.

How similar studies have gone: Biobanks in lung cancer and other cancers have supported numerous translational studies and some therapeutic advances, though this exact bronchial cancer biobank is a targeted, center-specific initiative.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Male or female patient aged over 18 years,
* Histologically or cytologically confirmed bronchial cancer,
* Treatment-naïve patient for the current cancer,
* Patient who has provided informed, written, and explicit consent,
* Patient affiliated with the French national health insurance system.

Exclusion Criteria:

* Patient with a WHO performance status ≥ 3,
* Pregnant and/or breastfeeding woman,
* Patient with a history of other cancers within the 5 years preceding inclusion,
* Patient for whom regular follow-up is considered impossible due to psychological, familial, social, or geographic reasons,
* Patient under legal protection (guardianship, curatorship, or judicial protection).

Where it's running

  • Centre Regional de Lutte Contre le Cancer - Centre Val d'Aurelle
    Montpellier, France, France
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.