drugset / Trial / NCT05917158

A Study of RC48-ADC Combined with JS001 for Postoperative Adjuvant Treatment of Upper Tract Urothelial Carcinoma

NCT05917158

Phase 2 Recruiting 30 enrolled Jinling Hospital, China
NaSingle-groupOpen-labelTreatment

Summary

This study will evaluate the efficacy and safety of intravenous RC48-ADC combined with JS001 in postoperative adjuvant therapy for HER2-positive upper tract urothelial carcinoma.

Timeline

Start
2022-11-23
Primary completion
2027-12
Completion
2028-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Disitamab Vedotin Monoclonal antibody 2 mg/kg Intravenous
Subject Toripalimab Monoclonal antibody 3 mg/kg Intravenous