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Clinical Trial Summary

This is a prospective, open, single-center clinical study of renal preservation therapy in high-risk upper urinary tract urothelial carcinoma patients . The study was conducted in accordance with the Good Practice for Quality Control of Clinical Trials for Pharmaceutical Products (GCP). Approximately 20 subjects will be enrolled to evaluate the efficacy and safety of RC48 (2.0 mg/kg intravenously every 3 weeks) combined with Tislelizumab (200mg intravenously every 3 weeks).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05912816
Study type Interventional
Source RenJi Hospital
Contact jiwei huang
Phone 8613651682825
Email jiweihuang@outlook.com
Status Recruiting
Phase Phase 2
Start date June 10, 2023
Completion date December 10, 2026