Study Comparing Repotrectinib and Crizotinib for Advanced ROS1-positive Non-Small Cell Lung Cancer

Sponsor: Bristol-Myers Squibb

Sponsor score: 60
Inactive

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.

Patient Parameters

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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