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:
- You have signed a consent form agreeing to take part in the study.
- You are 18 years of age or older.
- You have been diagnosed with an advanced or spreading type of lung cancer (non-squamous, non-small cell) that cannot be treated with curative treatments.
- Your lung cancer has been confirmed to have a specific gene change called an EGFR sensitizing mutation through a lab test.
- You are able to provide tumor tissue and blood samples for additional lab testing.
- Your cancer has stopped responding to treatment with all three generations of EGFR-targeted pills (known as EGFR TKIs).
- You are in reasonably good general health (able to carry out normal daily activities with little or no limitation) and are expected to live at least 12 more weeks.
- If you have cancer that has spread to the brain, any related brain surgery or radiation must have been completed at least 2 weeks before starting the trial, with side effects mostly resolved, and you must not have needed steroids or fluid-reducing medications for at least 4 weeks.
- You have at least one area of cancer in your body that can be measured on a scan.
- Your blood counts and organ function (such as liver and kidneys) are at acceptable levels before starting the trial.
Who may not be able to join:
- Your lung cancer has features of, or has changed into, a different type called small cell lung cancer.
- You received immunotherapy, antibody-based treatments, or similar cancer drugs within 4 weeks before starting the trial.
- You received chemotherapy, other anti-cancer drugs, or experimental treatments within 14 days before starting the trial.
- You received targeted radiation therapy within 7 days, or extensive radiation (including to large areas of bone marrow) within 28 days, before starting the trial.
- You are currently taking — or cannot stop taking — certain medications that strongly affect how the body processes drugs (called CYP3A4 inhibitors or inducers, including some herbal supplements like St. John's Wort) within 2–3 weeks before starting the trial.
- You are currently taking — or cannot stop taking — certain sensitive medications that interact with the study drug within 2 weeks before starting the trial (confirm with trial site).
- You are currently taking — or cannot stop taking — proton pump inhibitors (common heartburn/acid reflux medications) within 1 week before starting the trial.
- You have had major surgery within 4 weeks before starting the trial, or are planning major surgery during the trial.
- You still have side effects (grade 1 or higher, apart from hair loss) from a previous cancer treatment such as chemotherapy or radiation.
- Your cancer has spread in a way that is pressing on your spinal cord, or has spread to the membranes surrounding your brain or spinal cord.
- You have been diagnosed with another cancer within the past 2 years (some exceptions may apply — confirm with trial site).
- You have serious or poorly controlled conditions such as high blood pressure or a bleeding disorder.
- You have an ongoing or active infection, including hepatitis B, hepatitis C, or HIV.
- You have certain heart conditions or abnormalities, including irregular heart rhythms, a history of heart attack or stroke within the past 6 months, or a family history of certain heart rhythm problems (confirm with trial site).
- You have a history of deep vein blood clots or blood clots in the lungs within 4 weeks before starting the trial.
- You have a history of a lung condition called interstitial lung disease, or currently have active lung inflammation.
- You have ongoing severe nausea or vomiting, a chronic gut condition, difficulty swallowing, or have had part of your intestine removed in a way that might affect how your body absorbs the study medication.
- You have received a live vaccine within 4 weeks before starting the trial.
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: Lu, Shanghai Chest Hospital
Phone: +86 21 61095854
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
Number of participants with Dose-limiting Toxicities (DLTs); Number of participants with Adverse events (AEs)/Serious adverse events (SAEs); Objective Response Rate (ORR) as assessed by investigator per Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.