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Combination of DV and Tislelizumab for Renal Preservation in High-risk UTUC Patients

NCT05912816 PHASE2 RECRUITING

This is a prospective, open, multiple-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).

Details

Lead sponsorRenJi Hospital
PhasePHASE2
StatusRECRUITING
Enrolment20
Start dateSat Jun 10 2023 00:00:00 GMT+0000 (Coordinated Universal Time)
CompletionWed Dec 30 2026 00:00:00 GMT+0000 (Coordinated Universal Time)

Conditions

Interventions

Countries

China