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Can a drug make radiation work better against aggressive brain tumors?

NCT ID NCT00209989

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tested whether adding the drug ZARNESTRA to standard radiation therapy can slow tumor growth in people with glioblastoma, an aggressive brain cancer. Twenty-seven patients took the drug daily starting a week before radiation and continuing through treatment. The main goal was to see how long it took for the cancer to progress.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
ZARNESTRA (a drug that may make cancer cells more sensitive to radiation)
What this could lead to
If it works, this could point toward a way to slow glioblastoma progression by combining a drug with standard radiation.
What could go wrong
This is a small, early-phase study (27 people) with no control group, so results may not be conclusive. The drug may not improve outcomes or could add side effects.

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

Phase 2

Tests whether the treatment actually works, and watches for side effects, in a larger group.

Participants

27 people

The number who actually took part.

Start date

Oct 2005

Finished

Jun 2011

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 must have pathologically confirmed (histology or cytology), resectable or non resectable, glioblastoma multiforme with a size \< 5 cm on MRI if non resectable * Patients must be at least 7 days but no more than 2 months since surgery or biopsy. * Patients must have an ECOG Performance Status ≤ 2. * Patients must be aged 18 * Patient has signed the informed consent form Exclusion Criteria: * Patients with unresectable glioblastoma with a size \>5 cm on MRI * Patients with clinically apparent leptomeningeal metastases * Patients with uncontrolled seizures despite standard anticonvulsant therapy * Any prior systemic treatment (chemotherapy, immunotherapy, hormonal therapy) for glioblastoma multiforme * Significantly abnormal haematological status as judged by: Absolute neutrophil count (ANC) \< 1500/mm3 (1.5\*109/l) Platelet count \<100,000/mm3 (100\*109/l) * Serum bilirubin \>2 mg/dl (\>34 mmol/l) or Transaminase \>2.5x the upper limit of institutional normal or Creatinine \>1.5 mg/dl (\>132 mmol/l) * Inability to co-operate with the treatment protocol * Patients who cannot undergo imaging evaluations * Participation in an investigational drug trial in the 30 days prior to selection * Pregnant or nursing mothers. (Female patients of childbearing potential must use adequate contraception.) * Any malignancy within the past five years. Exceptions are: superficial basal cell carcinoma or non-metastatic squamous cell cancer of the skin, cervix cancer (cervical intra-epithelial neoplasia -CIN or FIGO stage 1) or prostate intra-epithelial neoplasia (PIN), biochemical relapse free for at least 3 years. * Any prior systemic chemotherapy in the past five years for any malignancy in the medical history * Any concurrent disease that in the opinion of the investigator would constitute a hazard for participating in this study * Known sensitivity to imidazole derivatives * Patients under law protection * Medical history of phlebitis or pulmonary embolism, thrombocytosis, myocardiopathy, or other relevant cardiac pathology (auricular flutter, auricular fibrillation) * Medical history of immuno-allergic pneumopathy

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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.

Contacts and locations

Locations

  • Centre Jean Perrin

    Clermont-Ferrand, France

  • Institut Claudius Regaud

    Toulouse, France

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Other studies related to the condition(s) this trial covers.