Brain Cancer Trial, Recruiting NCT03144167 Sponsor: Centre Hospitalier Universitaire, Amiens Condition: Brain Cancer
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Brain Cancer Trial, Recruiting

NCT03144167
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • Adults aged between 18 and 88 years who have been diagnosed with glioblastoma (a type of brain tumour), confirmed by laboratory testing of tumour tissue, and whose cancer has come back for the first time after standard treatment involving surgery, chemotherapy with temozolomide, and radiotherapy.
  • People whose blood test results meet specific thresholds for white blood cells, platelets, liver function, kidney function, and protein in urine (confirm exact values with trial site).
  • People who have health insurance coverage.
  • People who are able to give signed consent themselves, or, if unable to do so, whose nominated trusted person has provided consent on their behalf.

Who may not be able to join:

  • People who have had bleeding in the brain or tumour that is causing symptoms.
  • People with a Karnofsky performance score below 50% — a measure used by doctors to assess how well a person is able to carry out daily activities (confirm with trial site).
  • People who have previously been treated with a type of drug called an anti-angiogenic (a drug that targets blood vessel growth in tumours), or with a chemotherapy wafer called Gliadel, at any stage of their illness.
  • People with blood clotting disorders, particularly relevant to injectable treatments.
  • People with known reasons they cannot have an MRI scan, such as a pacemaker, metal fragments in the eye, or implanted electrodes.
  • People with a serious ongoing illness that is not well controlled, including another active cancer (except certain skin cancers that have been surgically removed, or cervical or breast cancer treated in its early, non-spreading stage).
  • People with an active infection that is not under control.
  • People with high blood pressure that remains above a certain level despite receiving treatment to control it.
  • People with unstable heart or artery disease, or a growing aneurysm (a bulge in a blood vessel wall).
  • People who have had a heart attack within the past 6 months.
  • People who have had a stroke or peripheral artery-related event within the past 6 months.
  • People with heart failure rated above a certain level of severity (confirm classification with trial site).
  • People with a bleeding disorder such as haemophilia or von Willebrand disease.
  • People with a kidney condition causing high levels of protein in the urine (above 2 g per 24 hours).
  • People who have coughed up blood within the past month.
  • People who have had a pulmonary embolism (a blood clot in the lungs) within the past month.
  • People who have had surgery (other than brain surgery or biopsy) within the past month, or who have a planned necessary surgery coming up.
  • People who have had a digestive fistula or bowel perforation that resolved less than 6 months ago.
  • People with a known allergy or sensitivity to bevacizumab or any of its ingredients, including components derived from Chinese hamster ovary cells or other similar biological antibodies.
  • People with severely reduced bone marrow function affecting blood cell production.
  • People who are pregnant or breastfeeding. The trial requires that effective contraception is in place during treatment where needed.
  • People who are under legal guardianship or have restricted legal freedom.
  • People who are currently participating in another clinical trial that has an exclusion period still in effect.
  • People who do not wish to take part in the study.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 12 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: +33322087511

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Centre Hospitalier Universitaire, Amiens
Registry
ClinicalTrials.gov
Start date
18 June 2019
Est. completion
20 January 2027

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Analyze 6-month survival defined as the time between inclusion in the protocol and death

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 12 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov