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Study identifier: NCT04928846 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Study to Assess Disease Activity and Adverse Events of Intravenous (IV) Telisotuzumab Vedotin Compared to IV Docetaxel in Adult Participants With Previously Treated Non-Squamous Non-Small Cell Lung Cancer (NSCLC)

Condition: Non Small Cell Lung Cancer  ·  Sponsor: AbbVie

PhasePhase 3
Planned participants768
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Cancer is a condition where cells in a specific part of body grow and reproduce uncontrollably. Non-small cell lung cancer (NSCLC) is a solid tumor, a disease in which cancer cells form in the tissues of the lung. The purpose of this study is to determine if telisotuzumab vedotin works better than docetaxel and to assess how safe telisotuzumab vedotin is in adult participants with NSCLC who have previously been treated. Change in disease activity and adverse events will be assessed. Telisotuzumab vedotin is an investigational drug being developed for the treatment of NSCLC. Participants will be randomly assigned a treatment of telisotuzumab vedotin or docetaxel at an 1:1 ratio. Each group receives intravenous (IV) infusion of telisotuzumab vedotin or IV infusion of docetaxel. Approximately 768 adult participants with c-Met overexpressing NSCLC will be enrolled in the study in approximately 330 sites worldwide. Participants will receive IV telisotuzumab vedotin every 2 weeks or docetaxel every 3 weeks until meeting study drug discontinuation criteria. At the conclusion of the study, participants who continue to demonstrate clinical benefit may be eligible to receive study treatment via an extension of the study, a rollover study, or through another mechanism. There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at a hospital or clinic. The effect of the treatment will…

This description comes directly from the study's public registry record.

Talk to the study team

ABBVIE CALL CENTER  ·  844-663-3742  ·  abbvieclinicaltrials@abbvie.com

Always discuss trial participation with your own doctor first.

Locations (317)

University of Alabama at Birmingham - Main /ID# 247074Birmingham, Alabama, United StatesActive Not Recruiting
Ironwood Cancer & Res Ctr /ID# 262446Chandler, Arizona, United StatesActive Not Recruiting
Mayo Clinic Arizona /ID# 255858Phoenix, Arizona, United StatesActive Not Recruiting
Onvida Health Yuma Medical Center /ID# 253625Yuma, Arizona, United StatesCompleted
City of Hope /ID# 243157Duarte, California, United StatesRecruiting
City Of Hope - Seacliff /ID# 263143Huntington Beach, California, United StatesRecruiting
City of Hope - Orange County Lennar Foundation Cancer Center /ID# 263144Irvine, California, United StatesRecruiting
City Of Hope - Antelope Valley /ID# 263138Lancaster, California, United StatesRecruiting
The Oncology Institute Of Hope & Innovation -East Los A /ID# 239774Los Angeles, California, United StatesCompleted
Eisenhower Medical Center /ID# 233189Rancho Mirage, California, United StatesCompleted
Premiere Oncology Foundation /ID# 253954Santa Monica, California, United StatesCompleted
Mayo Clinic Hospital Jacksonville /ID# 254688Jacksonville, Florida, United StatesCompleted

+ 305 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT04928846