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Brain chemical clues may predict who lives longer with aggressive cancer

NCT ID NCT03144167

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looks at whether certain brain chemicals can predict survival in people with glioblastoma (a fast-growing brain cancer) that has returned after standard treatment. Researchers will measure these chemicals with special scans 7 and 28 days after starting the drug bevacizumab. The goal is to find out early which patients are likely to benefit from this expensive treatment and avoid using it in those who won't.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 170 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jun 2019

Expected to finish

Jan 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Patients, between 18 and 88 years, with glioblastoma (histologically proven) in first relapse after conventional treatment by surgery and temozolomide and radiotherapy * Biological Criteria * Polymorphonuclear neutrophils\> 1500 / mm3 * Plates\> 100,000 / mm3 * SGOT-SGPT \<5 at the upper limit of normal (ULN) * Bilirubin \<1.5 x ULN * Creatinine \<1.5 LSN and creatinine clearance * Proteinuria \<1 g / 24 hours * Patient with health insurance * Consent signed by the patient if he is lucid, or failing that by the person of trust Exclusion Criteria: * Patients who can not benefit from bevacizumab for the following reasons: * Symptomatic cerebral or tumor hemorrhage * Karnofsky Index less than 50% or * Patients already treated with an antiangiogenic molecule or Gliadel (diagnosis and recurrence). * Coagulation disorders in case of injectable treatment (especially for avastin), * Contraindications known to the MRI: Pace Makers, foreign bodies intraocular, electrodes ... * Uncontrolled severe concomitant pathology, including another evolving cancer (with the exception of operative cutaneous tumors, in situ cancer of the cervix or breast treated). * Uncontrolled Infection * Uncontrolled hypertension (PAS\> 160 mm Hg) despite optimized treatment * Coronary artery disease or unstable arterial disease. Evolutionary aneurysm. * Myocardial infarction dating from less than 6 months. * Peripheral arterial or cerebrovascular accident occurring less than 6 months. * Heart Failure\> grade II NYHA * Hemorrhagic Disease (Hemophilia, Willebrandt ...) * Nephrotic syndrome with proteinuria\> 2 g / 24 h * History of haemoptysis dating less than 1 month. * Pulmonary embolism dating less than 1 month. * Surgical intervention (other than craniotomy or stereotactic biopsy) dating less than one month or essential and predictable surgery. * History of digestive fistula or intestinal perforation with resolution less than 6 months. * Hypersensitivity to bevacizumab or to any of the excipients mentioned in Composition. * Hypersensitivity to Chinese hamster ovary (CHO) cells or to other human or humanized recombinant antibodies. * Severe Myelosuppression * Pregnant or nursing. Contraception should be prescribed if necessary during treatment. * Persons deprived of liberty or placed under safeguard of justice (guardianship or curatorship), * Subject involved in another search including an exclusion period still in progress at pre-inclusion * Patient refusing to participate in the study

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

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  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • CHU Amiens Picardie

    RECRUITING

    Amiens, Picardie, 80054, France

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