drugset / Trial / NCT00555620

Study Of Sunitinib In Combination With Cisplatin/Capecitabine Or Oxaliplatin/Capecitabine In Patients With Advanced Gastric Cancer

NCT00555620

Phase 1 Completed 76 enrolled Pfizer
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of the study is to determine the safe and tolerable doses of sunitinib given together with either cisplatin and capecitabine or oxaliplatin and capecitabine in patients who have advanced gastric cancer who have not received prior chemotherapy for their advanced cancer

Timeline

Start
2008-05
Primary completion
2010-08
Completion
2011-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Capecitabine Small molecule 800 mg/m2 Oral
Subject Capecitabine Small molecule 1000 mg/m2 Oral
Subject Cisplatin Other / unclassified 80 mg/m2 Intravenous
Subject Oxaliplatin Small molecule 110 mg/m2 Intravenous
Subject Sunitinib Small molecule 25 mg Oral
Subject Sunitinib Small molecule 37.5 mg Oral

Indications