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NCT Number: NCT07173829

A Study to Better Understand the Biological and Molecular Mechanisms Involved in Glioblastoma Recurrence and Progression

BORDEAUX-GLIO is a prospective, monocentric study which will describe the molecular, immune and metabolic pathways involved in the progression and relapse of glioblastoma, using blood and tumor samples from patients who have undergone surgery for newly diagnosed or recurrent glioblastoma in the center.

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Key information

About this study

Glioblastoma is the most common and aggressive primary brain tumor in adults, whose relapse is almost systematic despite surgery, radiation therapy and temozolomide (STUPP protocol). Several clinical trials evaluating targeted therapy and immune checkpoint inhibitors have led to disappointed results. There is an unmet need to better understand the molecular and immune mechanisms underlying the invasion and progression of these tumors, in order to identify new therapeutic targets. The Bordeaux University Hospital is a leading French treatment center for glioblastoma, providing a large number of biological samples that can be analyzed at the molecular, immune and metabolic levels by specialized local teams.

Tumor tissue will be collected during patient surgery from primitive or recurrent glioblastoma, as well as blood samples, to perform transcriptomic and metabolomic analysis, including spatial transcriptomic and metabolomic, ex vivo generation of γδT lymphocytes and patient-derived xenografts.

A secondary objective is to develop, in preclinical models, innovative drugs with radiosensitizing effect and a γδT cell immunotherapy active against glioblastoma.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients of 18 years or older, with highly suspected glioblastoma on neuro-imagery
  • Planned surgical tumor resection,
  • No objection to participate in research
  • Signed genetic consent

Exclusion criteria

  • Patients under guardianship, curatorship or protective supervision
  • Taking immunosuppressants
  • Pregnant or breast-feeding women
  • Patients deprived of their liberty by judicial or administrative decision, or under psychiatric care

Treatment and study plan

Samples

Other

A 50 ml blood sample will be taken from the patient before the operation, and two 0.3 cm3 tumor samples will be taken during the operation from the resected tumor.

Primary outcomes

  1. Molecular mechanism

    Time frame: at inclusion (T0)

    Description of the molecular mechanism involved in the progression and recurrence of glioblastoma

  2. Metabolic mechanism

    Time frame: at inclusion (T0)

    Description of the metabolic mechanism involved in the progression and recurrence of glioblastoma.

  3. Immune mechanism

    Time frame: at inclusion (T0)

    Description of the immune mechanism involved in the progression and recurrence of glioblastoma

Study contacts

Contact information is provided by the study sponsor or research team.

Julien ENGELHARDT, Dr

CONTACT

[email protected]

05 56 79 55 77 ext. +33

Olivier BRANCHARD

CONTACT

[email protected]

05 57 82 06 97 ext. +33

Sponsors and collaborators

Lead sponsor

University Hospital, Bordeaux

Other

Collaborators

  • University of Bordeaux

Registry information

Official study title

A Prospective Study to Better Understand the Molecular, Immune and Metabolic Mechanisms Involved in Glioblastoma Recurrence and Progression, in the Aim to Identify New Therapeutic Targets and to Improve Current Therapies

Acronym: BORDEAUX-GLIO

Important dates

Study start
2025
Primary completion
2030
Study completion
2030
First posted
Sep 15, 2025
Registry last updated
Sep 15, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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