drugset / Trial / NCT04028245
A Study of Combination Spartalizumab and Canakinumab in Patients With Localized Clear Cell Renal Cell Carcinoma
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Canakinumab | Monoclonal antibody | 300 mg | Intravenous |
| Subject | Spartalizumab | Monoclonal antibody | 400 mg | Intravenous |