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Clinical Trial Summary

This study is designed to identify the target Non-Small Cell Lung Cancer (NSCLC) population(s) that overexpress c-Met (c-Met+) best suited for telisotuzumab vedotin therapy in the second line or third line setting (Stage 1) and then to expand the group(s) to further evaluate efficacy in the selected population(s) (Stage 2). After the Stage 2 global enrollment is completed, an additional cohort at an alternate dose level will evaluate the safety and efficacy of telisotuzumab vedotin (Stage 3).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03539536
Study type Interventional
Source AbbVie
Contact
Status Active, not recruiting
Phase Phase 2
Start date October 10, 2018
Completion date October 6, 2025

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