drugset / Trial / NCT04028245

A Study of Combination Spartalizumab and Canakinumab in Patients With Localized Clear Cell Renal Cell Carcinoma

NCT04028245

Phase 0 Completed 17 enrolled Columbia University Novartis · collab
NaSingle-groupOpen-labelTreatment

Summary

Primary Objective: * To confirm the safety and feasibility of canakinumab and spartalizumab (PDR-001) administered using a standard dose / schedule in the neo-adjuvant setting in renal cell carcinoma Secondary Objectives: * To assess the immune response to combination canakinumab and spartalizumab * To assess anti-tumor activity as measured by pathologic downstaging

Timeline

Start
2019-08-15
Primary completion
2025-03-14
Completion
2026-03-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Canakinumab Monoclonal antibody 300 mg Intravenous
Subject Spartalizumab Monoclonal antibody 400 mg Intravenous