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Clinical Trial 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.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00079612
Study type Interventional
Source Bayer
Contact
Status Completed
Phase Phase 2
Start date September 2002
Completion date January 2007

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