A Clinical Trial of a New Combination Treatment, Domvanalimab and Zimberelimab, Plus Chemotherapy, for People With an Upper Gastrointestinal Tract Cancer That Cannot be Removed With Surgery That Has Spread to Other Parts of the Body

Sponsor: Arcus Biosciences, Inc.

Sponsor score: 0

ClinicalTrials ID:NCT05568095

This Phase 3 trial evaluates domvanalimab and zimberelimab with chemotherapy versus nivolumab with chemotherapy for advanced gastric, GEJ, or esophageal adenocarcinoma. Eligible participants must have a confirmed diagnosis, ECOG status 0-1, and measurable lesions. Interventions include IV domvanalimab, zimberelimab, fluorouracil, leucovorin, oxaliplatin, and oral capecitabine.

Patient Parameters

Program Overview

This randomized Phase 3 open-label study will compare the efficacy of the T-cell immunoglobulin and immunoreceptor tyrosine-based inhibitory motif (ITIM) domain (TIGIT) monoclonal antibody domvanalimab, the anti programmed cell death protein 1 (PD-1) monoclonal antibody zimberelimab, and multiagent chemotherapy versus the anti PD-1 monoclonal antibody nivolumab and multiagent chemotherapy in the first-line treatment of participants with locally advanced unresectable or metastatic gastric, gastroesophageal junction (GEJ), and esophageal adenocarcinoma.

Eligibility Criteria

Inclusion Criteria

  • Capable of giving signed informed consent which is in compliance with the requirements and restrictions listed in the informed consent form (ICF) and in protocol.
  • Histologically confirmed diagnosis of locally advanced unresectable or metastatic gastric, GEJ, or esophageal adenocarcinoma.
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0-1.
  • At least one measurable target lesion per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1.

Key

Exclusion Criteria

  • Underlying medical or psychiatric conditions that, in the investigator's or sponsor's opinion, will make the administration of study-specified therapy hazardous, including but not limited to:
  • Interstitial lung disease, including history of interstitial lung disease or non-infectious pneumonitis. Active viral, bacterial, or fungal infections requiring parenteral treatment within 14 days of randomization.
  • Clinically significant cardiovascular disease, such as New York Heart Association Class II or greater cardiac disease or cerebrovascular accident within 3 months prior to randomization, unstable angina, or new onset angina within 3 months prior to randomization, myocardial infarction within 6 months prior to randomization, or unstable arrhythmia within 3 months prior to randomization.
  • History of prior solid-organ transplantation, including allogenic bone marrow transplantation.
  • Dementia, psychiatric, or substance abuse disorders that would interfere with satisfying the requirements of the trial.
  • Known human epidermal growth factor receptor 2 (HER-2) positive tumor.
  • Known untreated, symptomatic, or actively progressing central nervous system (CNS) (brain) metastases. Participants with leptomeningeal metastases are excluded from enrollment.
  • Received prior systemic treatment for locally advanced unresectable or metastatic gastric, GEJ, or esophageal adenocarcinoma.
  • Disease progression within 6 months of completion of neoadjuvant or adjuvant therapy.

Note: Other protocol defined Inclusion/Exclusion criteria may apply.

Locations

FACILITYZIPCITYSTATE
Genesis Cancer Center and Blood Institute - Hot Springs71913Hot SpringsArkansas
Kaiser Permanente - Los Angeles Medical Center90027Los AngelesCalifornia
Norris Comprehensive Cancer Center90033Los AngelesCalifornia
University of California Irvine Health Chao Family Comprehensive Cancer Center92868OrangeCalifornia
UCLA Health - Santa Monica Cancer Care90404Santa MonicaCalifornia
Yale Cancer Center06520New HavenConnecticut
Georgetown Lombardi Comprehensive Cancer Center22057Washington D.C.District of Columbia
SCRI - Florida Cancer Specialists - South Region Research Office33901Fort MyersFlorida
SCRI - Florida Cancer Specialists - North Region Research Office33705St. PetersburgFlorida
SCRI - Florida Cancer Specialists - Panhandle Research Office32308TallahasseeFlorida

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