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 aged 18 or older.
- People who have been diagnosed with a specific type and stage of lung cancer called locally advanced non-small cell lung cancer (NSCLC), confirmed by a laboratory test on a tissue or cell sample, at stage IIIA (not removable by surgery), IIIB, or IIIC.
- People aged 70 or older whose general physical condition is rated as 0 or 1 on a standard medical fitness scale (meaning fully active or able to carry out light work).
- People under 70 whose general physical condition is rated 0 or 1 on the same fitness scale and who also have significant other health conditions, OR whose fitness is rated as 2 on that scale.
- People whose treatment plan — specifically a sequential course of chemotherapy followed by radiotherapy — has been approved by a specialist medical team.
- People whose cancer can be measured using standard imaging criteria (called RECIST 1.1).
- People whose lung function tests show results at or above minimum required levels (confirm with trial site for specific values).
- People whose blood counts (white cells, platelets, and red blood cells) meet minimum required levels (confirm with trial site for specific values).
- People whose kidney and liver function test results meet minimum required levels (confirm with trial site for specific values).
- People who have national health insurance coverage.
- People of childbearing potential, and men who are sexually active with someone who could become pregnant, who agree to use an effective method of contraception during treatment and for 6 months after the last dose.
Who may not be able to join:
- People for whom immunotherapy or chemotherapy is medically unsuitable.
- People whose specialist medical team has approved a treatment plan where chemotherapy and radiotherapy are given at the same time (rather than one after the other).
- People with Stage I or Stage II non-small cell lung cancer.
- People who have previously received immunotherapy or chemotherapy for non-small cell lung cancer.
- People whose lung cancer is not a primary non-small cell lung cancer type.
- People whose tumour has specific genetic changes known as EGFR mutation, or ALK or ROS1 translocations.
- People whose cancer has spread to other parts of the body, including the brain.
- People who are not suitable for radiotherapy aimed at curing the disease, due to the size or position of the tumour.
- People with serious uncontrolled health conditions, such as a recent heart attack (within 3 months), unstable chest pain, severe heart failure, uncontrolled high blood pressure, advanced liver disease, severe infection, or heart muscle inflammation — or any other active condition that would make chemotherapy, immunotherapy, or radiotherapy unsafe.
- People who have lost 15% or more of their total body weight in the last 6 months.
- People whose general physical fitness is rated above 2 on the standard medical fitness scale.
- People with an active autoimmune disease (where the immune system attacks the body), or a history of certain autoimmune conditions such as lupus, inflammatory bowel disease, vasculitis, or others listed in the criteria (confirm with trial site for the full list). Note: autoimmune thyroid conditions managed with replacement therapy, and type 1 diabetes managed with insulin, are generally permitted.
- People with a history of certain lung scarring conditions (such as idiopathic pulmonary fibrosis or organised pneumonia), or signs of active lung inflammation on a scan.
- People who have taken immune-suppressing medications within the past 28 days, or steroid medications above a certain dose within the past 7 days (confirm with trial site for specific details; some exceptions apply).
- People with chronic active infections including tuberculosis, HIV, active hepatitis B, or active hepatitis C (some people with a history of treated hepatitis B or C may still be eligible — confirm with trial site).
- People who have had a severe infection (including COVID-19 requiring hospitalisation) within 4 weeks before starting the study treatment.
- People who have had another cancer within the past 3 years, or have a cancer that is still progressing (except certain skin cancers or non-invasive cervical cancers).
- People who have previously had radiotherapy to the chest area.
- People who have received a live vaccine within 28 days before starting chemotherapy.
- People who have had an organ or bone marrow transplant.
- People who have had major surgery within 4 weeks before starting treatment.
- People who are already taking part in another clinical treatment trial.
- People who are pregnant or breastfeeding.
- People under legal guardianship or curatorship.
- People unable to attend the required study visits or follow the study requirements for geographical, social, or physical reasons.
- People who are unable to understand what the study involves.
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: +33 1.56.81.10.45
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: 7 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.