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 who are able to understand the study information and are willing to sign a written consent form.
- People who are at least 18 years old.
- People who have been diagnosed through a tissue or cell sample with locally advanced or metastatic non-small cell lung cancer (a specific type of lung cancer that has spread or cannot be removed by surgery).
- People whose lung cancer has specific gene changes called EGFR mutations — specifically a deletion in exon 19 or a change called L858R in exon 21.
- People whose cancer shows high levels or extra copies of a protein/gene called c-Met, confirmed after previous treatment with a type of targeted therapy known as an EGFR-TKI.
- People who have at least one tumour that can be measured using standard imaging guidelines.
- People who are in relatively good general health, rated 0 or 1 on a standard medical scale used to measure how much a person's illness affects their daily activities (confirm with trial site).
Who may not be able to join:
- People who have previously been treated with MET inhibitors or therapies that target a protein called HGF.
- People whose cancer has specific gene changes called ALK or ROS1 mutations.
- People who have brain or central nervous system involvement that is causing symptoms, is not stable, or requires increasing doses of steroids to manage.
- People who are currently pregnant or breastfeeding.
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: +86-10-84148931
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
Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]).; Incidence of dose-limiting toxicities (DLT) as defined in the protocol.; Overall Response Rate (ORR)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.