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 give written consent and agree to follow the study schedule and requirements
- People aged 18 years or older
- People who have been diagnosed with stage I non-small cell lung cancer (confirmed by tissue testing under AJCC 9th edition guidelines), with a tumour measuring between 2cm and 4cm
- People whose post-surgery pathology report shows at least one higher-risk feature, such as cancer spreading into the lining around the lung, into blood or lymph vessels, through airspaces, or showing poorly differentiated or high-grade patterns
- People with a general health and activity level rated as fully active or with minor restrictions (ECOG 0 or 1)
- People whose tumour tests positive for a protein called PD-L1 at 1% or more
- People whose tumour does not carry certain gene changes known as EGFR or ALK sensitive mutations
- People who had a complete surgical removal of the tumour with no cancer left behind (called R0 resection)
- People who are within 8 weeks of surgery and have fully recovered from the operation
- People whose liver, kidneys, blood, and other organs are functioning adequately
Who may not be able to join:
- People who have already received any treatment for their current lung cancer, including radiotherapy, chemotherapy, immunotherapy, targeted therapy, or anti-angiogenesis therapy
- People who have previously had radiotherapy to the chest area, including the lung, oesophagus, middle chest, or breast
- People whose lung cancer is of a specific subtype called large-cell neuroendocrine carcinoma, or a mixed type that includes small-cell components
- People whose tumour carries EGFR or ALK sensitive mutations
- People who had only a smaller-scale lung surgery called a segmentectomy or wedge resection (rather than a larger lobe removal)
- People whose tumour involves the main airway tubes, or who have a collapsed or blocked lung related to the tumour
- People with an active autoimmune disease, or a history of an autoimmune disease that has come back
- People with a history of scarring or inflammation of the lung tissue (interstitial lung disease), including cases caused by drugs or previous radiation that required hormone treatment, or who currently have this condition
- People who have needed corticosteroid medicines above a certain dose (more than 10mg per day of prednisone or equivalent) or other immune-suppressing medicines within 14 days before being assigned to a study group
- People who have used certain immune-modifying medicines (such as interferon or interleukin-2) within 4 weeks before the first study dose
- People who have used herbal medicines intended to control cancer within 14 days before the first study dose
- People who have received a live or weakened vaccine within 4 weeks before joining, or who plan to receive one during the study or within 5 months after the last dose of the study drug
- People with a significant history of serious illness or conditions affecting the function of major organs or body systems, as judged by the study doctor
- People who have had a severe ongoing or active infection requiring systemic antibiotic, antifungal, or antiviral treatment (such as tuberculosis) within 14 days before the first study dose
- People known to have HIV infection
- People who have had an organ or stem cell transplant from another person
- People who have had another active cancer within the 2 years before joining, with some exceptions for certain early-stage or fully treated skin cancers, superficial bladder cancer, or pre-invasive cancers (confirm with trial site)
- People with certain personal circumstances, or alcohol or drug dependence, that may affect how the study drug is given, how results are interpreted, or that may increase health risks
- People who are pregnant or breastfeeding, or men and women who plan to try to conceive during the study
- People currently taking part in another interventional clinical trial (observational studies or follow-up-only study phases may be acceptable — confirm with trial site)
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: +86 134 3945 7872
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
2 year disease-free survival rate, 2y-DFS rate
Can't join this trial?
Data last synced from ClinicalTrials.gov: 7 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.