drugset / Trial / NCT03946917

JS001 Combined With Regorafenib in Patients With Advanced Colorectal Cancer

NCT03946917

NaSingle-groupOpen-labelTreatment

Summary

Colorectal cancer is one of the most common malignancies in China. Regorafenib is the standard multi-kinase inhibitor for refractory advanced colorectal cancer. In mice, regorafenib combined with anti-PD-1 was shown superior to regorafenib, which has not yet been verified in humans. JS001 is the Chinese anti-PD-1 monoclonal antibody for injection which has been approved for melanoma. This study is the first multi-center, open-label, phase I/II clinical trial to evaluate tolerability, safety and efficacy of JS001 in combination with regorafenib tablet in patients with MSS/MSI-L/pMMR, relapsed or metastatic colorectal cancer who have failed or can not tolerate fluorouracil, oxaliplatin and irinotecan based systemic treatment. The phase I clinical trial is to determine the maximum tolerated dose (MTD) and dose limiting toxicity (DLT) of regorafenib tablet in this regimen, and select an acceptable safe dose for the phase II clinical trial to further determine safety and efficacy of this combination regimen in patients with metastatic colorectal cancer.

Timeline

Start
2019-03-12
Primary completion
2020-05-01
Completion
2021-11-20

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Regorafenib Small molecule 80 mg Oral
Subject Regorafenib Small molecule 120 mg Oral
Subject Regorafenib Small molecule 160 mg Oral
Subject Toripalimab Monoclonal antibody 3 mg/kg Intravenous

Indications