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Clinical Trial Summary

Endostar is a anti-angiogenesis product and has been launched in China . The efficacy and safety have been defined. However, the compliance is unsatisfactory since routine i.v of Endostar is needed for 3 to 4 hours daily during one cycle of 14 days. The continuous intravenous infusion by using venous pump can improve the compliance.The comparative study in efficacy and safety has not been done concerning continuous and routine i.v.In addition, what patient can be benefited from Endostar have not been investigated. The biological markers, such as circulating endothelial cells,CECs, will be explored in the study.


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 NCT02283476
Study type Interventional
Source Jiangsu Simcere Pharmaceutical Co., Ltd.
Contact Zhao Yan, Doctor
Phone 18622221369
Email yanzhao@163.com
Status Not yet recruiting
Phase Phase 3
Start date November 2014
Completion date November 2017

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