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A Study to Assess Adverse Events and Change in Disease Activity of Intravenous (IV) Telisotuzumab Adizutecan, Monotherapy or in Combination With Osimertinib, Compared to Standard of Care in Adult Participants With Locally Advanced or Metastatic EGFR-Mutated Non-Squamous Non-Small Cell Lung Cancer

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NCT07155187 · readout ≤ 1,503 d

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

Phase
Phase 2/3
Status
Recruiting
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
490estimated
Sites
110
Countries
Australia, Austria, Belgium +16

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
Start2025-12-10actualWhen the study began enrolling
Primary completionSep 2030estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionSep 2030estimatedThe whole study's end, after follow-up
First posted2025-09-04actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-09actualThe 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

Interventions

  • Drug: Telisotuzumab Adizutecan
  • Drug: Standard of Care
  • Drug: Osimertinib

Primary outcomes

what the primary-completion date above is the date OF
Phase 2: Objective Response (OR) Assessed by the Blinded Independent Central Review (BICR)
measured Up to Approximately 69 Months
Phase 3: Progression-Free Survival (PFS) as assessed by the BICR
measured Up to Approximately 69 Months

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