Early Phase 1 Stomach 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:
- A tumor tissue sample must be available for testing.
- The patient must be 6 years old or younger at the time their brain or spinal tumor was confirmed by a tissue test (biopsy or surgery).
- The patient must have one of the following specific types of brain or spinal tumors: atypical teratoid rhabdoid tumor (ATRT), group 3 or group 4 medulloblastoma, pineoblastoma, CNS neuroblastoma, embryonal tumor with multi-layered rosettes (ETMR and related subtypes), medulloepithelioma, CNS embryonal tumor with rhabdoid features (INI-1 intact), or CNS embryonal tumor not otherwise specified — including cases where the cancer has spread or where only part of the tumor was removed.
- The patient must have had MRI scans of the brain and spine, both before and after surgery, using contrast dye.
- A spinal fluid sample (lumbar puncture) is strongly recommended but not required, and not having one will not disqualify the patient.
- The patient must be expected to live for more than 8 weeks from the time of diagnosis.
- The patient must be well enough to carry out at least half of normal daily activities, as measured by a standard childhood health score (Lansky score of 50 or above).
- The patient's kidneys must be working well enough (confirmed with a urine or scan test).
- The patient's heart must be functioning adequately (confirmed by an ultrasound or scan of the heart).
- The patient must be breathing comfortably at rest with an acceptable oxygen level (above 94% on room air).
- The patient's bone marrow must be producing enough blood cells (specific blood count levels required — confirm with trial site).
- The patient's liver must be working adequately (specific blood test levels required — confirm with trial site).
Who may not be able to join:
- Patients who are currently receiving any other cancer treatments or experimental treatments.
- Patients who have already received radiation therapy or chemotherapy for this tumor (steroid medications are the only exception).
- Patients who have another active cancer that is currently causing problems or requires treatment.
- Patients who are taking certain medications that affect how the body processes drugs, including some anti-seizure medicines (such as phenytoin, phenobarbital, or carbamazepine), certain antifungal medicines, rifampin, or St. John's Wort (confirm with trial site for the full list).
- Patients with serious uncontrolled health conditions such as uncontrolled diabetes, chronic kidney disease, active serious infections, liver disease, very high cholesterol, heart failure, irregular heartbeat, overactive parathyroid glands, or mental health conditions that would make it difficult to follow the study requirements.
- Patients who are known to have HIV, hepatitis B, or hepatitis C.
- Patients whose tumor type does not qualify — this includes certain other types of brain tumors such as SHH or WNT medulloblastoma, ependymoma, choroid plexus carcinoma, high-grade gliomas, diffuse midline gliomas, brain germ cell tumors, brain sarcomas, brain lymphomas, and certain leukemia-related growths.
- Patients (or their parents/guardians) who, in the doctor's opinion, would not be able to follow the study schedule and requirements.
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: Sylvia Cheng, BC Cancer Centre
Phone: 416-813-7654
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
To determine the feasibility of adding intrathecal (IT) topotecan and maintenance therapy after high dose chemotherapy for treatment of newly diagnosed HR-EBTs in patients less than 6 years of age.; To test the feasibility of centralized diagnostics and national tumour board review for clinical management of HR-EBTs; To establish a national HR infant brain tumor trial platform for future studies
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.