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 aged 18 to 75 years old
- People whose lung cancer has been confirmed as small cell lung cancer through a tissue or cell sample test
- People who have at least one tumour that can be measured on a scan, according to standard medical criteria
- People whose cancer has come back or gotten worse within 6 months of completing a first-line chemotherapy or combined chemotherapy and radiation treatment that included platinum-based drugs
- People whose general health and ability to carry out daily activities falls within an acceptable range on a standard medical scale (ECOG score of 0–2) (confirm with trial site)
- People whose life expectancy is estimated to be more than 3 months
- People who have largely recovered from the side effects of any previous cancer treatments, with only mild or no lasting effects remaining
- People whose major organs — including bone marrow, liver, kidneys, and blood clotting system — are functioning within acceptable levels on blood tests, and whose urine protein levels are within acceptable limits
Who may not be able to join:
- People diagnosed with a different but related type of lung cancer, such as large cell neuroendocrine lung carcinoma or combined small cell lung carcinoma
- People with cancer that has spread to the brain or spinal cord that is not well controlled, or that requires an increased dose of steroid medication (those with well-controlled brain metastases may still be considered)
- People who have fluid build-up around the lungs, abdomen, or heart that has not been controlled by drainage or other treatments in the 2 weeks before starting the study
- People who have been diagnosed with another cancer in the past 5 years, except for certain fully treated skin cancers or very early-stage cancers confined to one area
- People who have previously been treated with irinotecan, liposomal irinotecan, or certain anti-blood-vessel-growth drugs such as anlotinib or bevacizumab
- People taking certain medications that strongly affect how the body processes drugs (known as strong CYP3A4 inducers or inhibitors, or strong UGT1A1 inhibitors) within a short period before starting the trial (confirm timing with trial site)
- People who have received any other anti-cancer treatment — including radiation, chemotherapy, or immunotherapy — within 4 weeks before starting the trial
- People with serious uncontrolled heart conditions, such as unstable chest pain, recent heart attack, heart failure, or severe irregular heartbeat
- People who have had a serious lung disease — such as scarring of the lung tissue or severe radiation-related lung inflammation requiring steroids — within the 6 months before joining
- People who have had a blood clot in a vein or artery — such as a stroke, mini-stroke, deep vein clot, or pulmonary embolism — within the 6 months before joining
- People who have had bleeding problems or signs of bleeding within 3 months before screening, including stomach or bowel bleeding or certain blood vessel conditions
- People who have had a major surgical procedure within 4 weeks before starting the trial, or who are expected to need major surgery during the study
- People with wounds, ulcers, or broken bones that have not healed
- People whose scans show that the tumour is growing close to or involving major blood vessels in a way that could cause serious bleeding
- People with an active, uncontrolled infection (bacterial, viral, or fungal) that requires treatment
- People with active hepatitis B, hepatitis C, or HIV infection
- People with a known allergy or intolerance to the study drugs or their ingredients
- People with significant ongoing digestive or bowel problems, including liver disorders, bleeding, inflammation, blockage, or more than mild diarrhoea
- People who are pregnant or breastfeeding
- People considered unsuitable for the trial for any other reason, based on the treating doctor's judgement
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: Jialei Wang, Doctor, Fudan University
Phone: 021-64175590
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
Objective response rate(ORR)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 14 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.