Phase 2 Brain Cancer Trial, Recruiting
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:
- People who are willing to take part voluntarily, have been fully informed about the study, and are able to sign a consent form and follow all study procedures.
- People aged 18 or older (any gender).
- People who have been formally diagnosed with glioblastoma (GBM) through a tissue test.
- People who have had partial surgical removal of the tumour, or whose tumour has come back or grown, between 2 and 6 weeks after surgery and before radiation treatment has started.
- People whose blood, liver, kidney, and clotting function results meet specific minimum levels set by the trial (confirm with trial site for exact values).
- People whose heart pumping function (measured as left ventricular ejection fraction) is at least 50%.
- Women of childbearing potential whose pregnancy test is negative and who agree to use effective contraception from the time of signing the consent form until 6 months after the last chemotherapy dose.
- People whose thyroid hormone levels (TSH, FT4, and FT3) are within 10% of the normal range.
- People who are able to have a full eye examination including a dilated fundus check, slit lamp examination, and colour photographs of the back of the eye.
Who may not be able to join:
- People currently taking part in another clinical trial, or who finished treatment in a previous clinical trial less than 4 weeks ago.
- People who have had another cancer (other than GBM) in the past 3 years, or who have another active primary cancer that has not been cured.
- People who have previously had radiation therapy to the brain.
- People who are pregnant or breastfeeding.
- People who, after medical assessment, are found to have a medical reason they cannot safely receive radiation therapy.
- People with serious active health conditions that could interfere with the treatments used in this study.
- People with an active infection (bacterial, fungal, viral, or other) that requires treatment with antibiotics or other anti-infective medicines.
- People who, within the 6 months before joining the trial, have been diagnosed with heart failure, unstable chest pain (angina), serious uncontrolled heart rhythm problems, acute reduced blood flow to the heart, or a heart attack.
- People with a specific heart rhythm measurement (QTcF interval) greater than 480 milliseconds, unless this is caused by a bundle branch block (confirm with trial site).
- People with uncontrolled health conditions including, but not limited to, uncontrolled high blood pressure, active stomach ulcers, or bleeding disorders.
- People with a history of mental illness, or people who do not have full legal capacity to make decisions.
- People with any other medical history, condition, or abnormal test result that the trial doctors consider may interfere with the study or make participation unsuitable.
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.
Contact this trial
Phone: 8615157125533
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
Where this trial is recruiting
Primary endpoints
3 months PFS rate; 6 months PFS rate; 1-year PFS rate
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.