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This is a Study to Learn About How the Combination of the Study Medicines Sigvotatug Vedotin Plus Pembrolizumab Works in People With Non-small Cell Lung Cancer With High Levels of PD-L1.

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NCT06758401 · readout in 748 d

Sponsored by Pfizer (industry) · PFE — their whole pipeline →.

Phase
Phase 3
Status
Recruiting
Study type
Interventional
Design
Randomized · Single · Treatment
Enrollment
714estimated
Sites
372
Countries
Argentina, Australia, Austria +28

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
Start2025-07-23actualWhen the study began enrolling
Primary completion2028-09-05estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2029-03-01estimatedThe whole study's end, after follow-up
First posted2025-01-03actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-22actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Non-Small Cell Lung Cancer
  • Carcinoma, Non-Small-Cell Lung
  • Carcinoma, Non-Small-Cell Lung (NSCLC)

Interventions

  • Drug: Sigvotatug Vedotin
  • Drug: Pembrolizumab

Primary outcomes

what the primary-completion date above is the date OF
Overall Survival
measured Baseline to date of death from any cause (Approximately 2 years)
Progression Free Survival (PFS) assessed by blinded independent central review (BICR)
measured From Baseline to to date of first documentation of progression OR death (Approximately 2 year)

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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