drugset / Trial / NCT00712855

A Study of Mapatumumab in Combination With Sorafenib in Subjects With Advanced Hepatocellular Carcinoma

NCT00712855

Phase 1 Completed 23 enrolled GlaxoSmithKline GlaxoSmithKline · collab
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety and tolerability of escalating doses of mapatumumab in combination with sorafenib in subjects with advanced Hepatocellular Carcinoma who are positive for hepatitis B surface antigen or hepatitis C antibody.

Timeline

Start
2008-06
Primary completion
2011-08
Completion
2012-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Mapatumumab Monoclonal antibody 3 mg/kg Intravenous
Subject Mapatumumab Monoclonal antibody 10 mg/kg Intravenous
Subject Mapatumumab Monoclonal antibody 30 mg/kg Intravenous
Background Sorafenib Small molecule 400 mg Oral