120
Participants
Start Date
June 7, 2023
Primary Completion Date
June 6, 2025
Study Completion Date
June 6, 2026
vedicitumomab (Edisil, RC48)
intravenously for 6-8 cycles before surgery and postoperative radiotherapy, followed by Treatment with injectable recombinant humanized anti-HER2 monoclonal antibody-MMAE coupling agent vedicitumomab (Edisil, RC48) until 1 year or disease progression or intolerable toxicity in locally advanced patients , and until disease progression or intolerable toxicity in metastatic patients .
vedicitumomab in combination with pyrrolizidine
vedicitumomab in combination with pyrrolizidine
RC48 in combination with a platinum-based chemotherapeutic agent
RC48 in combination with a platinum-based chemotherapeutic agent
RC48 in combination with teraplizumab
RC48 in combination with teraplizumab
Peking Union Medical College
OTHER