drugset / Trial / NCT00970138

Apatinib Versus Placebo as a Third Line Treatment in Patients With Advanced or Metastatic Gastric Cancer

NCT00970138

Phase 2/3 Completed 141 enrolled Fudan University
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Apatinib is a tyrosin-inhibitor agent targeting at vascular endothelial growth factor receptor (VEGFR), and it's anti-angiogenesis effect has been viewed in preclinical tests. The investigators' phase I study has shown that the drug's toxicity is manageable and the maximum tolerable daily dose is 850 mg. The purpose of this study is to determine whether apatinib can improve progression free survival compared with placebo in patients with metastatic gastric carcinoma who failed two lines of chemotherapy.

Timeline

Start
2009-06
Primary completion
2010-10
Completion
2010-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Rivoceranib Small molecule 425 mg Oral
Subject Rivoceranib Small molecule 850 mg Oral

Indications