Early Phase 1 Stomach Cancer Trial, Recruiting NCT06942039 Sponsor: C17 Council Condition: Stomach Cancer
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Early Phase 1 Stomach Cancer Trial, Recruiting

NCT06942039
Recruiting Early Phase 1

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.

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 28 July 2026
Early Phase 1 studies are small, early exploratory studies that come before the main Phase 1 to 3 testing, so a standard phase success rate does not apply.

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

Status
Recruiting
Phase
Early Phase 1
Sponsor
C17 Council
Registry
ClinicalTrials.gov
Start date
23 September 2025
Est. completion
31 December 2030

Where this trial is recruiting

🇨🇦 Canada

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?

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: 28 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