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About
The study will compare the efficacy and safety of entrectinib with crizotinib in participants with advanced or metastatic ROS1 non-small cell lung cancer (NSCLC). The participants will self-administer oral entrectinib or crizotinib as described in the protocol and local prescribing information. Treatments will continue until progressive disease, unacceptable toxicity, death, or withdrawal from the study, whichever occurs first.
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Interventional model
Masking
220 participants in 2 patient groups
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Central trial contact
Reference Study ID Number: MO41552 https://forpatients.roche.com/
Data sourced from clinicaltrials.gov
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