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This is a standard Phase 1b and 2a, multi-center, study design that will examine the safety, tolerability, and maximum tolerated dose of tivozanib (AV-951) with this dosing schedule, as well as overall response rate of tivozanib (AV-951) administration in NSCLC.
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The Phase 2a portion of the study was not conducted
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17 participants in 1 patient group
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Data sourced from clinicaltrials.gov
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