CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 855 enrolled
Drug / intervention
Mitomycin, doxifluridine and cisplatin +1 moredrug
Likely dose
Mitomycin, doxifluridine and cisplatin 20mg/m2from record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00296335
NCT00296335Phase 3Completed

A Phase III Randomized Controlled Trial of Adjuvant Chemotherapy for Advanced Gastric Adenocarcinoma

Asan Medical Center·interventional·Posted Feb 27, 2006·Updated Feb 27, 2014

In Brief

A Phase 3 clinical trial evaluating Mitomycin, doxifluridine and cisplatin and Mitomycin and doxifluridine for Stomach Cancer. Completed, enrolled 855 participants across 1 site.

Detailed Summary

This is a phase III randomized study designed to evaluate the efficacy of mitomycin, doxifluridine, and cisplatin compared to mitomycin and doxifluridine.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsStomach Cancer
CountriesSouth Korea

Timeline

Phase 3CompletedFinished
20022003200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedFeb 27, 2006
Enrollment StartFeb 1, 2002
Primary CompletionNov 1, 2007
Study CompletionDec 1, 2009
TodayJul 2, 2026
Enrollment to primary: 5.8 yearsPosted 20.3 years ago

Interventions

Mitomycin, doxifluridine and cisplatindrug

Mitomycin-C 20mg/m2 intravenously (day 1), Doxifluridine 460-600mg/m2/day per oral (day 28- day 336), Cisplatin 60mg/m2 intravenously (day 28, day 56, day 84, day 112, day 140, and day 168)

Mitomycin and doxifluridinedrug

Mitomycin-C 20mg/m2 intravenously (day 1), Doxifluridine 460-600mg/m2/day per oral (day 28-day 84)