Study Comparing Repotrectinib and Crizotinib for Advanced ROS1-positive Non-Small Cell Lung Cancer
Sponsor: Bristol-Myers Squibb
ClinicalTrials ID:NCT06140836
This clinical trial is testing two drugs, repotrectinib and crizotinib, to see which is more effective and safe for treating patients with advanced non-small cell lung cancer (NSCLC) that has a specific genetic marker called ROS1-positive.
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Program Overview
The aim of this study is to compare the effectiveness and safety of two medications, repotrectinib and crizotinib, in patients with advanced non-small cell lung cancer (NSCLC) that has not been treated with certain types of cancer drugs before and has a specific genetic change known as ROS1-positive.
Eligibility Criteria
Inclusion Criteria
- Have a confirmed diagnosis of advanced non-small cell lung cancer (NSCLC).
- Have a specific genetic change in the cancer called ROS1-positive, confirmed by a test.
- Have at least one tumor that can be measured by scans.
- Have not been treated with certain cancer drugs known as tyrosine kinase inhibitors (TKIs) that work on ROS1-positive NSCLC.
- May have had one previous treatment for NSCLC.
- Be in relatively good health, with a performance status score of 2 or less, meaning fully active or able to do light work.
Exclusion Criteria
- Have cancer that has spread to the brain or the membranes surrounding the brain and is causing symptoms.
- Have had another type of cancer that needed treatment in the past two years, except for the skin cancers or completely removed in situ cancers.
- Have other known genetic changes in the tumor that can be targeted by treatments.
- Have significant heart disease that is active or was present in the last six months.
Note: There are additional criteria that may apply.
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