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 have been diagnosed with extensive-stage small cell lung cancer (a type of lung cancer that has spread), confirmed through a tissue or cell sample.
- People who have not yet received any systemic (whole-body) treatment for this type of lung cancer.
- People who have at least one tumour that can be measured on a scan, according to standard research measurement guidelines.
- People aged between 18 and 75 years.
- People whose general physical health and ability to carry out daily activities falls within a certain acceptable range, as assessed by a doctor using a standard scale (confirm with trial site).
- People who are expected to live for at least 3 months.
- People whose blood cell counts, kidney, liver, heart, and clotting functions all meet minimum levels set by the trial (confirm with trial site for the specific values).
- Women who could become pregnant must have a negative pregnancy test within 3 days before starting treatment and must agree to use highly effective contraception throughout the trial.
- Men must agree to use barrier contraception (such as condoms) during the trial.
- People who are willing and able to sign a consent form and follow the study procedures.
Who may not be able to join:
- People who have brain metastases (cancer that has spread to the brain) that are causing symptoms. Those with treated, stable, symptom-free brain metastases for at least one month without the need for steroids may still be considered.
- People who have previously had radiotherapy to the chest area for small cell lung cancer.
- People who have previously been treated with certain types of cancer medicines, including anti-angiogenic drugs (such as anlotinib or bevacizumab) or immune checkpoint therapies targeting PD-1 or PD-L1.
- People who have difficulty swallowing or have had major bowel or stomach surgery that could affect the ability to take oral (swallowed) medication.
- People who have fluid build-up around the lungs, heart, or abdomen that is not under control and requires repeated draining.
- People whose scans show that the tumour is growing into major blood vessels, or who are considered at high risk of serious bleeding by the treating doctor.
- People with a history of significant bleeding problems, including coughing up more than roughly one tablespoon of blood per day in the past 3 months, or any significant bleeding episode within 4 weeks before joining the trial.
- People who have had major surgery, an open biopsy, or a serious injury within 28 days before joining the trial.
- People who have had a blood clot or stroke (in an artery or vein) within the past 6 months, such as a stroke, deep vein thrombosis, or pulmonary embolism.
- People who have an active autoimmune disease that has required systemic (whole-body) treatment at any point in the 2 years before starting the trial.
- People who have any other medical condition that the treating doctor believes would increase risk or make participation in the trial unsuitable.
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: Dingzhi Huang, Doctor, Tianjin Medical University Cancer Institute and Hospital
Phone: 86-22-23340123
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
Progression-Free Survival (PFS)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 20 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.