drugset / Trial / NCT03113188

CBP501, Cisplatin and Nivolumab in Advanced Refractory Tumors

NCT03113188

Phase 1 Completed 47 enrolled CanBas Co. Ltd.
NaSingle-groupOpen-labelTreatment

Summary

This is a multicenter, open-label, phase 1b study of CBP501/cisplatin/nivolumab combination administered once every 21 days to patients with advanced solid tumors.

Timeline

Start
2017-10-25
Primary completion
2021-02-15
Completion
2021-02-15

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject CBP501 Peptide
Subject Cisplatin Other / unclassified
Subject Nivolumab Monoclonal antibody

Indications