drugset / Trial / NCT02404441

Phase I/II Study of PDR001 in Patients With Advanced Malignancies

NCT02404441

Phase 1/2 Completed 319 enrolled Novartis Pharmaceuticals
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this "first-in-human" study of PDR001 was to characterize the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD) and antitumor activity of PDR001 administered i.v. as a single agent to adult patients with solid tumors. By blocking the interaction between PD-1 and its ligands, PD-L1 and PD-L2, PDR001 inhibits the PD-1 immune checkpoint, resulting in activation of an antitumor immune response by activating effector T-cells and inhibiting regulatory T-cells.

Timeline

Start
2015-04-27
Primary completion
2020-07-21
Completion
2020-07-21

Drugs

EvaluationDrugModalityDoseRoute
Subject Spartalizumab Monoclonal antibody 1 mg/kg Intravenous
Subject Spartalizumab Monoclonal antibody 3 mg/kg Intravenous
Subject Spartalizumab Monoclonal antibody 5 mg/kg Intravenous
Subject Spartalizumab Monoclonal antibody 10 mg/kg Intravenous
Subject Spartalizumab Monoclonal antibody 300 mg Intravenous
Subject Spartalizumab Monoclonal antibody 400 mg Intravenous