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:
- You are 18 years of age or older
- You have been diagnosed with locally advanced or spreading (metastatic) non-small cell lung cancer (NSCLC) that has tested positive for an ALK gene change, confirmed through a tissue or cell sample
- You have had a full scan assessment (including a CT scan of the chest and upper abdomen, and an MRI of the brain) before starting the study treatment
- Your general health and ability to carry out daily activities falls within an acceptable range (rated 0, 1, or 2 on a standard medical scale)
Who may not be able to join:
- You have had another active cancer in the last 2 years (with some exceptions, such as certain skin, cervical, thyroid, breast, or prostate cancers — confirm with trial site)
- You have previously been treated with a type of targeted drug called an ALK TKI as a preventative (adjuvant) therapy, unless your cancer spread more than one year after finishing that treatment
- You have already received any systemic treatment (such as chemotherapy or targeted therapy) for your lung cancer after it became metastatic
- You have taken certain medications or foods that strongly affect how the body processes drugs (known as strong CYP3A inhibitors, strong CYP3A inducers, or certain narrow therapeutic index P-gp substrates) within 12 days before starting the study drug (confirm with trial site)
- You have a medical or mental health condition that the study doctor believes could make participation unsafe or unsuitable for you
- You are pregnant (confirmed by a positive pregnancy test)
- You are breastfeeding, or you are a woman who could become pregnant and are unwilling or unable to use a highly effective form of contraception during the study and for at least 35 days after the last dose of the study drug
- You are a man who could father a child and are unwilling or unable to use a highly effective form of contraception during the study and for at least 97 days after the last dose of the study drug
- You are currently taking part in another clinical trial that involves an active treatment (observational studies may be acceptable — confirm with trial site)
- You are unable to give your own legal consent, or are under guardianship or protective custody
- You are not registered with the French social security system
- You do not agree to allow your personal data to be collected for the study
- You are unable or unwilling to attend scheduled appointments, follow-up visits, and complete all parts of the study as required
- You are unable to answer the study's questions due to language barriers, psychological, social, or geographical reasons
- You are a member of the research team running this trial, or a close family member of someone on the research team
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: Pfizer CT.gov Call Center, Pfizer
Phone: 1-800-718-1021
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: 6 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.