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Clinical Trial Summary

This multicenter, randomized study will evaluate the efficacy and safety of apatinib compared to docetaxel treatment in patients with advanced gastric cancer. At the start of the trial, patients will be randomized to one treatment arm: Arm A: apatinib 850mg qd every 3 weeks; Arm B: docetaxel 60mg/m2 every 3 weeks. Tumor assessment will be done every 8 weeks according to RECIST 1.1. The primary endpoint is progression free survival (PFS).


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02409199
Study type Interventional
Source Shanghai Zhongshan Hospital
Contact Liu Tianshu, doctor
Phone +862152303355
Email liu.tianshu@zs-hospital.sh.cn
Status Recruiting
Phase Phase 2/Phase 3
Start date June 2015
Completion date March 2017

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