Phase 2 Epilepsy 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 have been newly diagnosed with a type of brain tumour called glioblastoma (located in the upper part of the brain), diagnosed according to the 2021 WHO brain tumour classification system
- People who are able to give their signed consent to take part
- People who are over 18 years of age
- People whose doctors have determined them suitable for the standard combination of chemotherapy and radiotherapy using a drug called temozolomide (a shortened, hypofractionated course of radiotherapy is not permitted)
- People who score 70 or above on a standard medical scale that measures ability to carry out daily activities (called the Karnofsky Performance Scale)
- People who are considered mentally able to understand their situation, including being aware of where they are, the time, and their circumstances
- People for whom a preserved sample of their tumour tissue is available for review by a central pathology team
- People whose blood tests show that their blood cell counts, liver, and kidney function are within acceptable ranges
Who may not be able to join:
- People who are scheduled to receive a shortened (hypofractionated) course of radiotherapy
- People who are currently pregnant or breastfeeding
- People who plan to become pregnant, or whose partner plans to become pregnant, during the course of the study
- People of childbearing potential who are not using, or not willing to use, a reliable form of contraception throughout the study (such as the pill, injections, implants, or an intrauterine device) — this does not apply to people who are surgically sterilised or have been post-menopausal for more than two years
- People with other serious ongoing medical conditions, such as kidney failure, liver problems, or significant heart disease
- People with a known or suspected history of not following medical instructions, or with drug or alcohol misuse issues
- People who may be unable to follow the study procedures, for example due to language barriers, psychological conditions, or dementia
- People who have taken part in another clinical trial involving an experimental drug within the 30 days before joining, or who are currently in another such trial
- People who have previously been enrolled in this same trial
- People who are members of the research team running this trial, or their family members or dependants
- People who have previously had radiotherapy to the brain, or any prior radiotherapy that might overlap with the planned treatment area
- People who have another active cancer that could interfere with the study treatment
- People whose heart tracing (ECG) shows an abnormality in a measurement called QTc that is greater than 450 milliseconds
- People for whom a contrast-enhanced brain MRI scan using a substance called Gadolinium is not safe or suitable
- People who have previously had an allergic or intolerance reaction to any of the drugs used in this study
- People who have had intolerance reactions to a group of medicines called sulfonamides or to salicylates (such as aspirin-related compounds)
- People with a condition called acute intermittent porphyria
- People with a known deficiency of an enzyme called glucose-6-phosphate dehydrogenase
- People currently taking any of the following medications: digoxin, cyclosporin, or methotrexate
- People with a history of serious skin or immune reactions to medications, including conditions known as exfoliative dermatitis, Stevens-Johnson Syndrome, toxic epidermal necrolysis, DRESS syndrome, or renal tubular acidosis
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
Principal Investigator: Hans-Georg Wirsching, MD, University Hospital and University of Zurich
Phone: +41432532928
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
PFS-6
Can't join this trial?
Data last synced from ClinicalTrials.gov: 7 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.