drugset / Trial / NCT03809013

A Open-label, Single-arm, Multicenter, Phase II Study of RC48-ADC to Evaluate the Efficacy and Safety of Subjects With HER2 Overexpressing Locally Advanced or Metastatic Urothelial Cancer

NCT03809013

Phase 2 Completed 64 enrolled RemeGen Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

This study will evaluate the efficacy and safety of intravenous RC48-ADC in patients with HER2 overexpressing locally advanced or metastatic urothelial cancer.

Timeline

Start
2019-01-07
Primary completion
2021-03-04
Completion
2023-06-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Disitamab Vedotin Monoclonal antibody 2 mg/kg Intravenous

Indications