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:
- Written consent has been provided by the patient or their legal representative
- The person is 18 years of age or older, of any gender
- A diagnosis of non-small cell lung cancer (a type of lung cancer) has been confirmed through laboratory testing of tissue or cell samples
- Genetic testing has confirmed the presence of a specific gene change (called an EGFR mutation, either classical or non-classical type)
- A diagnosis of leptomeningeal metastases (cancer that has spread to the membranes surrounding the brain and spinal cord) has been confirmed through symptom assessment, imaging scans, and/or spinal fluid testing, following established specialist diagnostic guidelines
- Both people newly diagnosed with leptomeningeal metastases and those whose cancer has progressed after previous cancer treatments may be considered
- The person has a performance status score of 0 to 3 on the ECOG scale, which broadly means they are able to carry out at least some self-care activities (confirm with trial site)
- Previous radiation therapy or surgery to the brain or spinal cord is permitted
- People experiencing symptoms related to the central nervous system (brain or spinal cord) may be considered, provided those symptoms are not life-threatening
- People who are able to have children must agree to use highly effective contraception during the trial and for 12 months after treatment ends
Who may not be able to join:
- People who currently have a cancer other than non-small cell lung cancer
- People who have had another cancer diagnosis within the past 5 years, with the exception of certain skin, cervical, or breast conditions that have been successfully treated
- People with serious digestive tract conditions that could affect how medication is absorbed, such as peptic ulcers or inflammatory bowel disease
- People with severe or uncontrolled health conditions, including uncontrolled high blood pressure, uncontrolled diabetes, active bleeding, or active infections such as hepatitis B, hepatitis C, or HIV
- People with a history of certain types of lung inflammation (interstitial lung disease), including inflammation caused by medication or previous radiation, or any current signs of this condition
- People with significant heart rhythm problems (such as a prolonged QT interval above 500ms) or heart failure with reduced pumping function
- People who are pregnant or breastfeeding
- People who received a live vaccine within the 4 weeks before starting the trial
- People who are currently participating in, or have participated in, another clinical trial within the past 4 weeks
- People with other serious medical, psychiatric, or laboratory conditions that, in the opinion of the trial investigators, could increase risk or interfere with the trial results, or who may be unable to complete the trial for any reason
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: Qiming Wang, MD, Henan Cancer Hospital
Phone: +86 15515521691
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
OS
Can't join this trial?
Data last synced from ClinicalTrials.gov: 6 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.