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Study of Telisotuzumab Vedotin (ABBV-399) in Participants With Previously Treated c-Met+ Non-Small Cell Lung Cancer

Active, not recruiting · Phase 2 · NCT03539536

Conditions: Non-small Cell Lung Cancer

At a glance

Research payments reported, 2025
$112,755
U.S. investigators named
15
Sites paid
12
Planned or actual enrollment
270

About the trial

Sponsor
AbbVie
Tested
Telisotuzumab vedotin (drug)
Dates
Started 2018-10-10; completion 2026-08
Results posted
Not yet

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).

From ClinicalTrials.gov, last updated 2025-11-05. Full record, eligibility and contacts (opens in a new tab)

Industry funding

AbbVie Inc. reported $112,755 in research payments for this study in 2025 (36 payments).

Products named: Emrelis

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.