Clinical Trials

Sponsor: AbbVie, Inc

Sponsor Study ID: M18-868

Study Title: A Phase 3 Open-Label, Randomized, Controlled, Global Study of Telisotuzumab Vedotin (ABBV-399) Versus Docetaxel in Subjects with Previously Treated c-Met Overexpressing, EGFR Wildtype, Locally Advanced/Metastatic Non-Squamous Non-Small Cell Lung Cancer (M18-868)

NCT Number: NCT04928846

Phase: III

Protocol Type: Treatment

Age Group: Adults

Disease Sites: Lung

Study Objectives: The primary objective is to determine if telisotuzumab vedotin improves progression-free survival (PFS) per ICR assessment and/or Overall Survival (OS) compared to docetaxel in the following nested populations: Subjects with c-Met high overexpressing, EGFR wildtype, nonsquamous NSCLC and all subjects with c-Met overexpressing, EGFR wildtype, nonsquamous NSCLC



Study Documents    
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