drugset / Trial / NCT02467361

A Study of BBI608 Administered in Combination With Immune Checkpoint Inhibitors in Adult Patients With Advanced Cancers

NCT02467361

Phase 1 Completed 104 enrolled Sumitomo Pharma America, Inc.
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This is an open label, multi-center, Phase 1/2 study of BBI608 administered in combination with immunotherapy in adult patients with advanced cancers. The goal of the study is to determine the RP2D of BBI608 in combination with each of the immunotherapeutic agents.

Timeline

Start
2015-08
Primary completion
2021-01-29
Completion
2021-01-29

Drugs

EvaluationDrugModalityDoseRoute
Subject Ipilimumab Monoclonal antibody 3 mg/kg Intravenous
Subject Napabucasin Small molecule 240 mg
Subject Napabucasin Small molecule 480 mg
Subject Nivolumab Monoclonal antibody 3 mg/kg Intravenous
Subject Pembrolizumab Monoclonal antibody 2 mg/kg Intravenous

Indications