drugset / Trial / NCT06405685

Nimotuzumab Plus AG in Pancreatic Cancer With Liver Metastasis

NCT06405685 ↗

NaSingle-groupOpen-labelTreatment

Summary

This is a prospective, open-label, single arm clinical study. The main purpose of the study is to evaluate the clinical efficacy and safety of Nimotuzumab combined with AG in the treatment of pancreatic cancer with liver metastasis. Patients will receive Nimotuzumab plus AG as conversion therapy, and imaging assessments (according to RECIST V.1.1 criteria) will be performed every two cycles (every two months) of conversion therapy. The main endpoint is R0 resection rate. Additional end points included resection rates, overall survival (OS), objective response rate (ORR), safety, etc.

Timeline

Start
2023-04-27
Primary completion
2025-10-30
Completion
2025-10-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Gemcitabine Small molecule 1000 mg/m2 —
Subject Nab-paclitaxel Small molecule 125 mg/m2 Intravenous
Subject Nimotuzumab Monoclonal antibody 400 mg Intravenous