drugset / Trial / NCT04636515

A Phase Ⅱ Study of F520 in Patients With Urothelial Carcinoma

NCT04636515

Phase 2 Unknown 80 enrolled Shandong New Time Pharmaceutical Co., LTD
NaSingle-groupOpen-labelTreatment

Summary

This is a multicenter, Phase 2 study to evaluate the efficacy and safety of the anti- programmed cell death-1(PD-1) monoclonal antibody F520 in participants with locally advanced or metastatic Urothelial Cancer (UC).

Timeline

Start
2021-01
Primary completion
2022-03
Completion
2022-09

Drugs

EvaluationDrugModalityDoseRoute
Subject F520 Monoclonal antibody 200 mg

Indications