drugset / Trial / NCT06155383

Perioperative Disitamab Vedotin Plus Toripalimab and XELOX in Gastric or Gastroesophageal Junction Adenocarcinoma.

NCT06155383

Phase 2 Recruiting 90 enrolled RemeGen Co., Ltd.
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of perioperative Disitamab Vedotin plus Toripalimab and XELOX versus Disitamab Vedotin plus Toripalimab versus XELOX in subjects with HER2-expressing resectable locally advanced gastric or gastroesophageal junction adenocarcinoma.

Timeline

Start
2023-11-27
Primary completion
2025-01-31
Completion
2027-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Capecitabine Small molecule 1000 mg/m2 Oral
Subject Disitamab Vedotin Monoclonal antibody 2.5 mg/kg Intravenous
Subject Oxaliplatin Small molecule 130 mg/m2 Intravenous
Subject Toripalimab Monoclonal antibody 3 mg/kg Intravenous