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Clinical Trial Summary

This is an open label, dual cohort ,phase II study to explore efficacy and safety of cadonilimab(PD-1/CTLA-4 Bispecific Antibody) combined with standard regimen neoadjuvant treatment in urothelial carcinoma(UC) and renal cell carcinoma(RCC), with evaluating successful preservation rate of bladder/kidney.


Clinical Trial Description

UC and RCC confirmed by histopathology or cytology prior have not received systematic treatment, who had indications for surgical resection and were difficult to preserve organ function after surgery or were partially resection but the patients have a strong desire to preserve organ function. This study enrolled 20 cases in each cohort of UC and RCC,pts received neoadjuvant treatment containing cadonilimab for no more than 6 cycles. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06427057
Study type Interventional
Source Tongji Hospital
Contact Liu Huang, Clinical Professor
Phone 63639656
Email huangliu@tjh.tjmu.edu.cn
Status Not yet recruiting
Phase Phase 2
Start date July 1, 2024
Completion date December 1, 2027