Phase 1 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:
- Adults aged 18 or older who have one or more brain tumors and are already planned to have brain surgery to remove or take a sample of the tumor.
- People who also have cancer that has spread to the lining of the brain or spinal cord, as long as they also have a brain tumor that requires surgery or biopsy.
- People who have previously had radiation to the brain or any other cancer treatments — there is no limit on prior treatments for any group in this trial.
- People with a performance score of 60 or above on a standard scale used to measure ability to carry out daily activities (confirm with trial site).
- People with a life expectancy of more than 12 weeks.
- People who have had enough time since their last cancer treatment for any side effects from that treatment to have settled, as assessed by the trial doctor.
- People whose blood test results, taken within 7 days before starting the study treatment, meet all of the following standards:
- White blood cell levels (specifically infection-fighting cells) are at or above a minimum threshold, without having received a certain type of blood cell booster injection in the week before treatment starts.
- Platelet counts (cells that help blood clot) are at or above the required level, without needing ongoing transfusions or boosters to stay there, and without having received a platelet transfusion in the week before treatment starts.
- Haemoglobin (a measure of red blood cells) is at or above the required level, without needing ongoing transfusions or boosters to maintain it, and without having received a red blood cell transfusion in the week before treatment starts.
- Kidney function is at or above a minimum level, based on a standard calculation.
- Liver enzyme levels (markers of liver health) are within an acceptable range, with slightly higher allowances for people who have cancer that has spread to the liver.
- A measure of how well the liver processes waste products is within an acceptable range, with allowances for people who have a known liver condition called Gilbert's syndrome or liver metastases.
Who may not be able to join:
- People with a known allergy or sensitivity to the study drug or any of its ingredients. (Note: people who are allergic to a type of dye used in MRI scans may still be considered, with precautions or alternative imaging at the discretion of the principal investigator.)
- People who have been diagnosed with more than one separate primary cancer within the past 3 years — with the following exceptions:
- Certain skin cancers that have been fully removed.
- A very early-stage cervical condition that has been treated.
- Slow-growing or low-risk blood or immune conditions that the treating doctor considers unlikely to progress during the trial, such as certain types of leukaemia or a condition called MGUS.
- Any cancer that has been treated with the aim of a full cure.
- Other solid tumours that have been treated with the aim of a full cure.
- For people with metastatic breast cancer: a cancer in the other breast.
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: Nelson Moss, MD, Memorial Sloan Kettering Cancer Center
Phone: 212-639-7075
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
ORR (overall response rate)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 8 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.