drugset / Trial / NCT02639234

Vigil™ + Nivolumab in Advanced Non-Small Cell Lung Cancer

NCT02639234

Phase 2 Withdrawn Gradalis, Inc.
NaSingle-groupOpen-labelTreatment

Summary

This is an open label phase 2 study to evaluate the combination of Vigil™ and nivolumab in advanced or metastatic NSCLC that is progressive on or after one prior platinum-based systemic therapy. Patients meeting study eligibility criteria will receive Vigil™ every 2 weeks (for a minimum of 4 and a maximum of 12 doses) and nivolumab every 2 weeks. The combination of Vigil™ and nivolumab will demonstrate a higher objective response rate (ORR) than the historical ORR of single agent nivolumab in patients with advanced NSCLC.

Timeline

Start
2016-03
Primary completion
2017-03
Completion
2017-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Nivolumab Monoclonal antibody 3 mg/kg Intravenous
Subject Vigil Vaccine 1e+07 cells Intravenous