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.
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
| Parameter | Options |
|---|
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
| FACILITY | ZIP | CITY | STATE |
|---|---|---|---|
| Genesis Cancer Center and Blood Institute - Hot Springs | 71913 | Hot Springs | Arkansas |
| Kaiser Permanente - Los Angeles Medical Center | 90027 | Los Angeles | California |
| Norris Comprehensive Cancer Center | 90033 | Los Angeles | California |
| University of California Irvine Health Chao Family Comprehensive Cancer Center | 92868 | Orange | California |
| UCLA Health - Santa Monica Cancer Care | 90404 | Santa Monica | California |
| Yale Cancer Center | 06520 | New Haven | Connecticut |
| Georgetown Lombardi Comprehensive Cancer Center | 22057 | Washington D.C. | District of Columbia |
| SCRI - Florida Cancer Specialists - South Region Research Office | 33901 | Fort Myers | Florida |
| SCRI - Florida Cancer Specialists - North Region Research Office | 33705 | St. Petersburg | Florida |
| SCRI - Florida Cancer Specialists - Panhandle Research Office | 32308 | Tallahassee | Florida |
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