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

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NCT03539536

Sponsored by AbbVie (industry) · ABBV — their whole pipeline →.

Phase
Phase 2
Status
Active, not recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
270actual
Sites
252
Countries
Australia, Belgium, Bulgaria +23

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2018-10-10actualWhen the study began enrolling
Primary completionJul 2026estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionAug 2026estimatedThe whole study's end, after follow-up
First posted2018-05-29actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-11-05actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Non-small Cell Lung Cancer

Intervention

  • Drug: Telisotuzumab vedotin — also filed as ABBV-399

Primary outcomes

what the primary-completion date above is the date OF
Overall Response Rate (ORR) (Stage 1 and Stage 2)
measured Up to approximately 3 years
Number of Participants with Adverse Events (Alternate dose cohort)
measured Up to approximately 3 years

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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