drugset / Trial / NCT03484923

Study of Efficacy and Safety of Novel Spartalizumab Combinations in Patients With Previously Treated Unresectable or Metastatic Melanoma

NCT03484923

Phase 2 Completed 196 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupOpen-labelTreatment

Summary

The primary purpose of this study is to evaluate the efficacy of novel spartalizumab (PDR001) combinations in previously treated unresectable or metastatic melanoma

Timeline

Start
2018-09-10
Primary completion
2022-12-30
Completion
2022-12-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Canakinumab Monoclonal antibody 200 mg Subcutaneous
Subject Capmatinib Small molecule 400 mg Oral
Subject Ribociclib Small molecule 600 mg Oral
Subject Spartalizumab Monoclonal antibody 400 mg Intravenous
Subject ieramilimab Monoclonal antibody 600 mg Intravenous

Indications