drugset / Trial / NCT01938612

A Phase I, Open-Label, Multicentre Study to Evaluate the Safety, Tolerability and Pharmacokinetics of MEDI4736 in Patients With Advanced Solid Tumours

NCT01938612

Phase 1 Completed 269 enrolled AstraZeneca
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This is a phase I, open-label, multicentre study of MEDI4736 administered intravenously with a standard 3+3 dose-escalation phase to evaluate safety, tolerability, and pharmacokinetics in patients with advanced solid tumor followed by an expansion phase in patients with advanced solid tumors.

Timeline

Start
2013-09-12
Primary completion
2018-03-01
Completion
2020-11-25

Drugs

EvaluationDrugModalityDoseRoute
Subject Durvalumab Monoclonal antibody 10 mg/kg Intravenous
Subject Durvalumab Monoclonal antibody 20 mg/kg Intravenous
Subject Tremelimumab Monoclonal antibody 1 mg/kg Intravenous

Indications