drugset / Trial / NCT00079612

Study of Nexavar (Sorafenib, BAY 43-9006) in Patients With Advanced Refractory Cancer

NCT00079612 ↗

Phase 2 Completed 501 enrolled Bayer Amgen · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of the study is to: * Find out if BAY 43-9006 prevents the growth of tumors * For patients who have stable cancer status after 3 months of treatment if it is safer and/or more effective to continue to give BAY 43-9006 or to stop giving BAY 43-9006 at that time. * Find out how long the effect of BAY 43-9006 is on tumors. To assess the safety of BAY 43-9006 (sorafenib) in the treatment of advanced refractory cancers. * Measure the amount of BAY 43-9006 and some of its targets in the blood stream in some patients.

Timeline

Start
2002-09
Primary completion
—
Completion
2007-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Sorafenib Small molecule 800 mg —

Indications