drugset / Trial / NCT01644968

Phase 1 Study of Anti-OX40 in Patients With Advanced Cancer

NCT01644968

Phase 1 Completed 30 enrolled Providence Health & Services
RandomizedParallel-groupOpen-labelTreatment

Summary

This study is designed to determine the safety and highest tolerated dose of anti-OX40 in patients with advanced cancer.

Timeline

Start
2003-11
Primary completion
2009-05
Completion
2017-04

Drugs

EvaluationDrugModalityDoseRoute
Subject KLH Unknown 1 mg Subcutaneous
Subject Tetanus toxoid vaccine Vaccine 0.5 ml
Subject anti-OX40 Monoclonal antibody 0.1 mg/kg
Subject anti-OX40 Monoclonal antibody 0.4 mg/kg
Subject anti-OX40 Monoclonal antibody 2 mg/kg