drugset / Trial / NCT01693562

A Phase 1/2 Study to Evaluate MEDI4736

NCT01693562

Phase 1/2 Completed 1022 enrolled MedImmune LLC
NaSingle-groupOpen-labelTreatment

Summary

This is a multicenter, open-label, first-time-in-human study with a standard 3+3 dose-escalation phase in participants with advanced solid tumors followed by an expansion phase in participants with advanced solid tumors. An exploration cohort has been added to determine the safety using every 4 weeks (Q4W) dosing.

Timeline

Start
2012-09-05
Primary completion
2020-02-28
Completion
2020-02-28

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Durvalumab Monoclonal antibody 0.1 mg/kg Intravenous
Subject Durvalumab Monoclonal antibody 0.3 mg/kg Intravenous
Subject Durvalumab Monoclonal antibody 1 mg/kg Intravenous
Subject Durvalumab Monoclonal antibody 3 mg/kg Intravenous
Subject Durvalumab Monoclonal antibody 10 mg/kg Intravenous
Subject Durvalumab Monoclonal antibody 15 mg/kg Intravenous
Subject Durvalumab Monoclonal antibody 20 mg/kg Intravenous

Indications