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:
- Adults aged 18 to 75 years (male or female)
- People with a laboratory-confirmed diagnosis of a specific type of lung cancer called non-squamous non-small cell lung cancer (NSCLC), at stages IB, II, IIIA, or IIIB (N2)
- People who have not received any treatment for their lung cancer before surgery
- People whose cancer can be removed with surgery, and whose lung function is strong enough to tolerate that surgery
- People whose cancer does not have specific gene changes known as EGFR mutations or ALK translocation
- People who have at least one measurable tumour, as assessed by standard imaging criteria
- People with a good general level of physical functioning (rated 0 or 1 on a standard medical scale, meaning fully active or able to carry out light activity)
- People with adequate organ function confirmed through screening tests
Who may not be able to join:
- People whose lung cancer is confirmed to be small cell lung cancer, or certain other tumour types including neuroendocrine carcinoma, sarcoma, salivary gland tumour, mesenchymal tumour, or a mixed type with mainly squamous cell features
- People whose tumour has grown into nearby important structures and is causing symptoms or requiring medical treatment
- People with a type of tumour located at the top of the lung called a Pancoast tumour
- People who have a cancerous tumour nodule in the opposite lung
- People with known or suspected cancer spread to the brain or other distant parts of the body
- People who have used Chinese herbal medicines, traditional Chinese medicinal products with anti-tumour properties, or immune-modifying drugs within 2 weeks before the first study treatment
- People who need ongoing steroid treatment throughout the body, or who have received other immune-suppressing therapy within 7 days before the first study treatment
- People who have had a blood clot in an artery within the 6 months before the first study treatment
- People who have had a blood clot in a deep vein, a clot in the lungs, or another serious blood clot in a vein within 3 months before the first study treatment
- People with a history of lung inflammation (pneumonitis) that required steroid treatment, or significant lung disease (or suspected lung disease seen on imaging during screening)
- People with active or uncontrolled medical conditions (confirm with trial site)
- People with a history of immune deficiency disease
- People who have had an active autoimmune disease requiring treatment throughout the body at any point in the 2 years before the first study treatment
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: 15005136320
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
Pathologic Complete Response (pCR) rate; Safety parameters: the incidence of all adverse events (AEs); Safety parameters: the incidence of treatment-emergent adverse events (TEAEs); Safety parameters: the incidence of immune-related adverse events (irAEs); Safety parameters: the incidence of adverse events of special interest (AESIs); Safety parameters: the incidence of serious adverse events (SAE); Safety parameters: the relatedness of infusion-related reactions (IRRs) to the investigational product and their severity; Safety parameters: the surgery delay rate; Proportion of subjects with abn...
Can't join this trial?
Data last synced from ClinicalTrials.gov: 22 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.