Feasibility Study of Adjuvant Treatment With S-1 in Patients After R0-Resection of Adenocarcinoma of the Stomach and Esophagogastric Junction

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

October 6, 2015

Primary Completion Date

March 1, 2019

Study Completion Date

March 6, 2020

Conditions
Adenocarcinoma,StomachAdenocarcinoma, Esophagogastric Junction
Interventions
DRUG

S-1

"18 cycles S-1, orally administered twice daily D1-14, q 3 wks~S-1 starting dose: 2 x 30 mg/m\^2 body surface area (BSA), D1-14, q 3 wks First dose reduction: 2 x 25 mg/m\^2 BSA, D1-14, q 3 wks Second dose reduction: 2 x 20 mg/m\^2 BSA, D1-14, q 3 wks"

Trial Locations (1)

Unknown

Klinikum der Universität München, Campus Großhadern, München

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Nordic Pharma SAS

INDUSTRY

collaborator

Taiho Pharmaceutical Co., Ltd.

INDUSTRY

lead

AIO-Studien-gGmbH

OTHER

NCT02564367 - Feasibility Study of Adjuvant Treatment With S-1 in Patients After R0-Resection of Adenocarcinoma of the Stomach and Esophagogastric Junction | Biotech Hunter | Biotech Hunter