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Study to Evaluate Monotherapy and Combination Immunotherapies in Participants With PD-L1 Positive Non-small Cell Lung Cancer

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NCT04262856

Sponsored by Arcus Biosciences, Inc. (industry) · RCUS — their whole pipeline →. With Gilead Sciences.

Phase
Phase 2
Status
Completed
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
151actual
Sites
44
Countries
Australia, Canada, Hong Kong +4

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
Start2020-05-28actualWhen the study began enrolling
Primary completion2025-07-09actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-07-09actualThe whole study's end, after follow-up
First posted2020-02-10actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-06-15actualThe 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
  • Nonsquamous Non Small Cell Lung Cancer
  • Squamous Non Small Cell Lung Cancer
  • Lung Cancer

Interventions

  • Drug: Domvanalimab — also filed as AB154
  • Drug: Etrumadenant — also filed as AB928
  • Drug: Zimberelimab — also filed as AB122

Primary outcomes

what the primary-completion date above is the date OF
Objective response rate (ORR)
measured From randomization until the first documentation of disease progression or death from any cause, whichever occurs first (up to approximately 3-5 years)
Progression-free survival (PFS)
measured From randomization until the first documentation of disease progression or death from any cause, whichever occurs first (up to approximately 3-5 years)

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