drugset / Trial / NCT02359058

A Study of Ramucirumab Combination Therapy in Japanese Participants Who Have Advanced Stomach Cancer

NCT02359058

Phase 1 Completed 18 enrolled Eli Lilly and Company
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The main purpose of this study is to evaluate the safety, tolerability, pharmacokinetics and antitumor response of ramucirumab in combination with platinum/fluoropyrimidine regimens in Japanese participants with advanced gastric/gastrooesophageal junction cancer who have not received chemotherapy.

Timeline

Start
2015-02
Primary completion
2016-07
Completion
2016-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Capecitabine Small molecule 1000 mg/m2 Oral
Subject Cisplatin Other / unclassified 60 mg/m2 Intravenous
Subject Cisplatin Other / unclassified 80 mg/m2 Intravenous
Subject Oxaliplatin Small molecule 100 mg/m2 Intravenous
Subject Ramucirumab Monoclonal antibody 8 mg/kg Intravenous
Subject S-1 Small molecule 40 mg/m2 Oral

Indications