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Clinical Trial Summary

Patients will be treated with irinotecan (150 mg/m2) followed by oxaliplatin (85 mg/m2) on day 1 and S-1 (80 mg/m2/day) from day 1 to 14 every 3 weeks. Patients will receive up to a planned treatment of maximum 12 cycles of chemotherapy. Response assessment will be performed every 2 cycles of chemotherapy.


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00506571
Study type Interventional
Source National Cancer Center, Korea
Contact Kyung Hae Jung, M.D.Ph.D
Phone +82-31-920-1611
Email khjung@ncc.re.kr
Status Recruiting
Phase Phase 2
Start date July 2007
Completion date June 2010

See also
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Recruiting NCT00507143 - Study of Genetic Polymorphisms of Drug Transporters and Orphan Nuclear Receptors on Treatment Effects of Irinotecan N/A