drugset / Trial / NCT04659369

Study of Pharmacokinetic, Safety, Immunogenicity and Efficacy of CMAB819 and Nivolumab in R/M HNSCC

NCT04659369

Phase 1 Terminated 21 enrolled Taizhou Mabtech Pharmaceutical Co.,Ltd
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to compare the pharmacokinetic, safety, immunogenicity and efficacy of CMAB819 and Nivolumab in subjects with recurrent or metastatic head and neck squamous cell carcinoma., after failure of prior platinum-based chemotherapy.

Timeline

Start
2020-09-24
Primary completion
2023-10-16
Completion
2023-10-16

Drugs

EvaluationDrugModalityDoseRoute
Comparator Nivolumab Monoclonal antibody 480 mg Intravenous