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An Open Label Study Evaluating the Efficacy and Safety of Etrumadenant (AB928) Based Treatment Combinations in Participants With Metastatic Colorectal Cancer.

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NCT04660812

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

Phase
Phase 1/2
Status
Completed
Study type
Interventional
Design
Randomized · Single · Treatment
Enrollment
227actual
Sites
44
Countries
France, Italy, South Korea +3

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
Start2021-05-10actualWhen the study began enrolling
Primary completion2025-09-05actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-09-05actualThe whole study's end, after follow-up
First posted2020-12-09actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-10-20actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Metastatic Colorectal Cancer

Interventions

  • Drug: AB680
  • Drug: Etrumadenant — also filed as AB928
  • Drug: Zimberelimab — also filed as AB122
  • Drug: Bevacizumab
  • Drug: m-FOLFOX-6 regimen
  • Drug: Regorafenib

Primary outcomes

what the primary-completion date above is the date OF
Cohort A and B - Progression-free Survival (PFS)
measured From randomization until death from any cause (up to approximately 3-7 years)
Cohort C - Objective Response Rate (ORR)
measured From randomization until death from any cause (up to approximately 3-7 years)
Number of Participants With Treatment-emergent Adverse Events
measured Up to approximately 10 Months

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