Pancreatic Cancer Clinical Trial
Official title:
Pharmacokinetic and Pharmacodynamic Study of S-1 and Its Effects in Patients With the Digestive Organ Cancer With Reference to Genetic Polymorphism and Activity of CYP2A6 and DPD
NCT number | NCT00197431 |
Other study ID # | S-12005 |
Secondary ID | |
Status | Recruiting |
Phase | Phase 2 |
First received | September 12, 2005 |
Last updated | March 21, 2006 |
Start date | January 2004 |
S-1 is a novel oral fluorouracil antitumor drug that consists of tegafur which is a prodrug of 5-fluorouracil (5-FU); 5-chloro-2,4-dihydropyridine (CDHP), which inhibits dihydropyrimidine dehydrogenase (DPD) activity; and potassium oxonate (Oxo), which reduces gastrointestinal toxicity. 5-FU is metabolized by CYP2A6 and DPD. In this study, the researchers investigate the influences of differences in activities of CYP2A6 and DPD on pharmacokinetics and pharmacodynamics of S-1 and clinical outcomes in digestive organ cancer patients treated with S-1.
Status | Recruiting |
Enrollment | 0 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | |
Gender | Both |
Age group | 20 Years to 85 Years |
Eligibility |
Inclusion Criteria: - Patients with digestive organ cancer Exclusion Criteria: - Patients without digestive organ cancer |
Allocation: Non-Randomized, Endpoint Classification: Pharmacokinetics/Dynamics Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Japan | Hamamatsu University School of Medicine | Hamamatsu | Shizuoka |
Lead Sponsor | Collaborator |
---|---|
Hamamatsu University |
Japan,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Whether the differences in activities of CYP2A6 and DPD affect pharmacokinetics and pharmacodynamics of S-1 and clinical outcomes | |||
Secondary | Side effect and motility of patients treated with S-1 |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
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