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Clinical Trial Summary

Evaluation of DC-CIK cells combined TACE treatment for HCC


Clinical Trial Description

60 patients with Hepatocellular Carcinoma, who had received Transcatheter Arterial Chemoembolization (TACE) , will be randomly divided into group A (receive DC-CIK+ TACE treatment) or group B (just receive TACE), and the randomize ratio will be 1:1. ;


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 NCT02487017
Study type Interventional
Source Shenzhen Hornetcorn Bio-technology Company, LTD
Contact Xiangzhong Liu, Professor
Phone 0535-6606236
Email xiangzhong8686@sina.com
Status Recruiting
Phase Phase 2
Start date May 2015
Completion date December 2018

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