The purpose of this study is to evaluate the efficacy and tolerability of the maintenance
treatment of tegafur-uracil (UFT) after the standard first-line chemotherapy in advanced
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Full eligibility criteria for NCT02903498
Ages eligible for Study
18 Years to 75 Years
Genders eligible for Study
Accepts Healthy Volunteers
Histologically confirmed advanced or metastatic adenocarcinoma of the stomach
ECOG PS 0-2
At least one measurable or evaluable lesion in the first-line chemotherapy (5-FU based regimen: ECF/EOF/EOX/FOLFOX/XELOX) with the efficacy evaluation of non-PD
Adequate hepatic,renal,heart, and hematologic functions (platelets ≥75×109/L, neutrophil≥1.5×109/L, hemoglobin≥80 g/L, serum creatinine ≤1.5mg/dl, total bilirubin
≤1.5mg/dl, and serum transaminase≤2.5×the ULN)
Receiving more or more than 2 regimens of chemotherapy
Pregnant or lactating women
History of other malignancies except cured basal cell carcinoma of skin and carcinoma in-situ of uterine cervix
Neuropathy, brain, or leptomeningeal involvement
Clinically relevant coronary artery disease or a history of a myocardial infarction within the last 12 months or high risk/uncontrolled arrhythmia
Uncontrolled significant comorbid conditions and previous radiotherapy
All locations for NCT02903498
View full eligibility
Tris trial is registered with FDA with number: NCT02903498. The sponsor of the trial is Fudan University and it is looking for 58 volunteers for the current phase.
Official trial title: Phase II Study of the Maintenance Treatment of UFT (Uracil and Tegafur) After First-line
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