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 to 75 years at the time of signing the consent form
- People who have been confirmed through laboratory testing (tissue or cell samples) to have small cell lung cancer
- People with limited-stage disease (a specific stage range assessed through scans and procedures such as PET-CT, bronchoscopy, or biopsy) where the treating surgeon considers the tumour removable with the goal of no cancer cells left behind — this includes certain tumour sizes and lymph node involvement, but excludes tumours that have grown into surrounding structures such as the heart, windpipe, or spine, and excludes more than one lymph node station being affected (confirm with trial site)
- People who have not previously received any radiotherapy, chemotherapy, immunotherapy, surgery, or other systemic cancer treatments
- People with a performance status score of 0 or 1 on the ECOG scale, meaning they are fully active or have only minor limitations in physical activity (confirm with trial site)
- People whose life expectancy is greater than 3 months
- People whose blood counts and organ function are within an acceptable range within 30 days before joining, as required to safely receive platinum-based chemotherapy
- People without any medical reasons preventing them from receiving immunotherapy
Who may not be able to join:
- People whose tumour testing shows a different type of lung cancer called non-small cell lung cancer (NSCLC)
- People who have cancer that has spread to the brain, whether currently active or previously treated but now considered inactive
- People who have a history of, currently have, or show signs of interstitial lung disease (a group of conditions involving scarring or inflammation of the lungs), including pulmonary fibrosis or radiation-related lung inflammation
- People who have been taking steroid medications (corticosteroids) systemically within 14 days before the first study treatment
- People who have previously received radiotherapy, chemotherapy, immunotherapy, surgery, or other systemic cancer treatments
- People who have had any other active cancer within the 2 years before joining
- People who are pregnant, breastfeeding, or planning to become pregnant during the study
- People with serious or uncontrolled heart or blood vessel disease at the time of joining
- People who have or have had active autoimmune or inflammatory diseases
- People with a history of primary immune system deficiency disorders
- People with a current active infection
- People who have had active bleeding problems within 6 months before starting the study treatment, including vomiting blood, severe coughing up of blood, or blood in the stool
- People with wounds that are not healing, active stomach ulcers, or bone fractures
- People whom the trial doctor considers unsuitable for participation 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: +86-18121299888
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
One-year Event-free Survival Rate (1-year EFS Rate)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 19 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.