Phase 2 Epilepsy Trial, Recruiting NCT05664464 Sponsor: University of Zurich Condition: Epilepsy
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Phase 2 Epilepsy Trial, Recruiting

NCT05664464
Recruiting Phase 2

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.

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 7 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

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

Status
Recruiting
Phase
Phase 2
Registry
ClinicalTrials.gov
Start date
1 January 2023
Est. completion
1 June 2026

Where this trial is recruiting

🇨🇭 Switzerland

Primary endpoints

PFS-6

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: 7 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