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 between 18 and 75 years old
- People who have been diagnosed with non-small cell lung cancer confirmed through a tissue or cell sample, with additional genetic testing required if the cancer type is adenocarcinoma to rule out certain gene mutations (EGFR/ALK)
- People whose cancer has been staged as stage IIIA or IIIB (a specific sub-type involving lymph nodes no larger than 3cm, without spread beyond the lymph node capsule), confirmed through imaging or tissue biopsy of the lymph nodes in the chest
- People whose cancer — including the main tumour and any affected lymph nodes — has been assessed by a team of surgeons and specialists as potentially removable by surgery
- People who have at least one measurable tumour area based on standard imaging measurement guidelines
- People with a good general activity level (able to carry out daily activities with little or no restriction, as rated on a standard medical scale)
- People with no previous history of any other cancer
- People who have never received any treatment for their lung cancer, including surgery, radiation, chemotherapy, targeted therapy, or immunotherapy
- People whose heart and lung function meets the required levels — including breathing capacity and heart pumping function within acceptable ranges, as assessed by a surgeon
- People whose blood, liver, and kidney test results fall within the acceptable ranges required by the trial (confirm with trial site for specific values)
- People who are able and willing to use effective contraception from the time of signing the consent form until 180 days after the last dose of the study drug; women of childbearing age must also have a negative pregnancy test within 7 days before starting the study drug
- People who are willing to take part voluntarily and who have read, understood, and signed the informed consent form
Who may not be able to join:
- People whose cancer cannot be fully removed through surgery
- People who have an active autoimmune disease or a history of autoimmune conditions (such as certain types of inflammation affecting the eyes, gut, liver, pituitary gland, blood vessels, heart, kidneys, or thyroid); some exceptions may apply for certain conditions (confirm with trial site)
- People with immune deficiency conditions, including HIV infection, active hepatitis B, hepatitis C, or a combination of hepatitis B and C
- People with large, hard-to-control fluid build-up in the chest, abdomen, or around the heart
- People who have needed regular steroid medication (above a certain dose) or other immune-suppressing medications within the 14 days before starting the trial; some exceptions apply for inhaled or skin-applied steroids (confirm with trial site)
- People who have received anti-cancer vaccines or immune-stimulating treatments (such as interferon or similar therapies) within one month before starting the trial
- People currently taking part in another clinical trial, or who finished a previous clinical trial less than 4 weeks (or 5 half-lives of the trial drug) before starting this one
- People with a history of or current serious lung conditions such as pulmonary fibrosis, interstitial lung disease, or significant loss of lung function
- People who have had major surgery, an open biopsy, or a serious injury within 28 days before joining the trial
- People who have previously had an organ transplant or a bone marrow/stem cell transplant from another person
- Women who are pregnant or breastfeeding, or people who are unwilling or unable to use effective contraception
- People with a known allergy or intolerance to any of the study drugs
- People the trial investigators consider unsuitable for any other 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
Phone: +86 571 8812 8161
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 EFS rate
Can't join this trial?
Data last synced from ClinicalTrials.gov: 13 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.