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ProofPrincip IntraTu TCells SinglDoseImmunCheckpoinInhib Gastro-Esophage Adenocarcinoma w/ARID1a Mu
RECRUITINGEarly 1Sponsored by University of California, Irvine
Actively Recruiting
PhaseEarly 1
SponsorUniversity of California, Irvine
Started2026-05-25
Est. completion2027-01
Eligibility
Age18 Years+
Healthy vol.Accepted
Locations1 site
View on ClinicalTrials.gov →
NCT06824363
Summary
This is a proof of principle clinical trial determining efficacy of single dose dualimmune checkpoint inhibitors to increase intra-tumoral T cells in esophageal, gastroesophageal junction, and gastric adenocarcinomas. These are subjects who have not previously been treated for their disease, who are willing to undergo biopsy procedures, who's disease has not spread to other parts of the body, who's tumors have ARID1A mutations.
Eligibility
Age: 18 Years+Healthy volunteers accepted
Inclusion Criteria: * Non metastatic GEC including locally advanced unresectable * Treatment naïve * Histologically proven adenocarcinoma of the esophagus or the stomach with ARID1a mutation either by liquid biopsy (ctDNA) or tissue NGS/WES * MSI-Stable or pMMR * Age ≥ 18 years * Body weight \> 66 pounds * ECOG ≤ 2 * Repeat biopsy feasible * No clinically significant autoimmune disease Exclusion Criteria: * Patients with known metastatic disease * Prior systemic treatment for esophagus, GEJ, or the stomach adenocarcinoma * Patients with uncontrolled autoimmune disease per investigator discretion * Inability or refusal to undergo biopsy procedures to obtain tissue samples
Conditions5
CancerEsophageal AdenocarcinomaMalignant Solid TumorSolid Tumor, AdultStomach Adenocarcinoma
Interventions2
Locations1 site
Chao Family Comprehensive Cancer Center, University of California, Irvine
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Actively Recruiting
PhaseEarly 1
SponsorUniversity of California, Irvine
Started2026-05-25
Est. completion2027-01
Eligibility
Age18 Years+
Healthy vol.Accepted
Locations1 site
View on ClinicalTrials.gov →
NCT06824363