Phase 2 Lung 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:
- People aged 18 to 75 years old, of any gender
- People with a good general performance level, able to carry out normal daily activities with little or no limitation (confirm with trial site what this means for specific circumstances)
- People who have been diagnosed with non-small cell lung cancer confirmed through a tissue or cell sample
- People whose cancer has spread to the brain and has gotten worse after a previous first-line cancer treatment
- People whose brain metastases meet specific size and volume requirements — either measurable tumours that have not been treated with radiation, or tumours treated with a targeted form of radiotherapy that were smaller than a certain size (confirm with trial site for exact measurements)
- People who showed a positive response to a previous immunotherapy treatment (checkpoint inhibitor) at their first assessment
- People whose brain tumours, if previously treated with radiation, received a total radiation dose within safe limits for surrounding brain structures
- People with measurable brain tumours visible on MRI that are large enough to be measured accurately and repeatedly
- People who have had all areas of cancer outside the brain assessed by scan (such as CT or PET-CT) within 14 days before starting the trial
- People who have had a brain MRI scan within 14 days before starting the trial
- People whose estimated survival is greater than 12 weeks
- People of childbearing potential who agree to use effective contraception during the trial, and who have a negative pregnancy test before starting
- People who are not currently breastfeeding
- People with adequately functioning organs (as assessed by the trial site)
- People who are willing and able to give informed consent and follow all study requirements, including visits, tests, and treatment schedules
Who may not be able to join:
- People who have previously experienced severe (grade 3–4) toxic effects on the brain or pituitary gland from prior treatment
- People who do not have any measurable brain tumours that have not already been treated with radiation
- People whose cancer has spread to the lining of the brain or spinal cord (meningeal metastasis)
- People who have not completed a required waiting period after their last chemotherapy or targeted therapy (at least 3 weeks), or after brain tumour surgery (at least 2 weeks)
- People with significant autoimmune diseases
- People who have previously been treated with a type of immunotherapy called a CTLA-4 inhibitor
- People who have had another cancer in the past 5 years or who currently have another cancer
- People with a history of severe allergic reaction to any monoclonal antibody or to components of the study drug
- People with a history of, or currently having, non-infectious lung inflammation (pneumonitis) or interstitial lung disease that has required treatment with steroid medicines
- People who have had a serious infection within 4 weeks before starting the trial
- People who have a history of organ transplant or bone marrow/stem cell transplant from a donor
- People who have been taking high-dose steroid medicines or other immune-suppressing drugs within 14 days before starting the trial
- People with significant heart or cardiovascular disease
- People currently enrolled in another interventional clinical trial at the same time
- People who have received a live vaccine within 30 days before starting the trial, or who plan to receive one during the study
- People with a known history of mental illness, or substance, alcohol, or drug misuse
- People who are pregnant or breastfeeding
- People with any other medical condition, treatment history, or abnormal test result that the trial site determines could affect the study results or the person's wellbeing
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
Phone: +8613875898127
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
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Trial details
Where this trial is recruiting
Primary endpoints
iORR
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Data last synced from ClinicalTrials.gov: 15 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.