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Clinical Trial Summary

Phase 2 evaluation of capecitabine in patients with advanced or recurrent squamous cell carcinoma of the skin.


Clinical Trial Description

Participants are to receive 500 mg/m² of capecitabine orally (PO) twice daily (BID) on days 1 to 14. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed up for 2 years. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01823679
Study type Interventional
Source Stanford University
Contact
Status Terminated
Phase Phase 2
Start date March 2013
Completion date May 2014

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