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Clinical Trial Summary

The purpose of the study is: Find out if patients receiving sorafenib will live longer. Find out if sorafenib has any effect on patient reported outcomes. Find out if sorafenib prevents the growth of or shrinks liver tumors and/or their metastases. Determine the pharmacokinetics (PK) in patients with liver cancer.


Clinical Trial Description

The following abbreviations were used in the Adverse Event section:

- international normalized ratio (inr)

- Common Terminology Criteria for Adverse Events (ctcae)

- Not Otherwise Specified (nos)

- Gastrointestinal (gi)

- Central nervous system (cns)

- Absolute Neutrophil Count (anc)

- Alanine aminotransferase (ALT)

- Aspartate aminotransferase (AST)

- Creatine phosphokinase (cpk)

- Gammaglutamyltransferase (ggt)

- Genitourinary (gu)

- Atrioventricular (av) ;


Study Design

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


Related Conditions & MeSH terms


NCT number NCT00105443
Study type Interventional
Source Bayer
Contact
Status Completed
Phase Phase 3
Start date March 2005
Completion date November 2008

See also
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