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A Safety and Efficacy Study of Treatment Combinations With and Without Chemotherapy in Adult Participants With Advanced Upper Gastrointestinal Tract Malignancies

← catalyst calendar

NCT05329766 · readout ≤ 165 d

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

Phase
Phase 2
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
332actual
Sites
43
Countries
Canada, Chile, France +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
Start2022-06-10actualWhen the study began enrolling
Primary completionJan 2027estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionJun 2027estimatedThe whole study's end, after follow-up
First posted2022-04-15actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-29actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Gastrointestinal Tract Malignancies

Interventions

  • Drug: Domvanalimab
  • Drug: Quemliclustat
  • Drug: Zimberelimab
  • Drug: Fluorouracil
  • Drug: Leucovorin
  • Drug: Oxaliplatin

Primary outcomes

what the primary-completion date above is the date OF
Number of Participants with Adverse Events (AEs)
measured Up to 18 months
Objective Response Rate (ORR) as measured by Response Evaluation Criteria in Solid Tumors (RECIST) v1.1
measured Up to 18 months

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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