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Clinical Trial Summary

the purpose of this study is to evaluate the efficacy and safety of aptinib in patients with advanced HCC


Clinical Trial Description

HCC The is a common malignancy in the world, especially in China. Advanced HCC treatment is difficult and the prognosis is poor, which is still a great challenge and threat to the medical profession. The advent of the molecular targeted drug, Sola, has made the treatment dilemma of advanced HCC a breakthrough, but the efficacy and economic health ratio is far from satisfactory. After Sola, many new molecular targeted drugs were studied, but failed.

Although multiple treatment options, but for HCC Patient-recommended treatment programs require systematic treatment and surgery, TACE , local ablation and radiotherapy and other multidisciplinary means of combination, the selection of appropriate patients, appropriate means and timing to achieve individualized treatment.

1. Aptinib Union TACE can be generated through embolization and angiogenesis by the dual target of vascular suppression;2. TACE induces hypoxia, leading to an increase in the number of hypoxia-inducing factors that increases VEGF and PDGFR , while VEGF the and PDGFR may be important factors that induce tumor recurrence by stimulating tumor angiogenesis. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03398122
Study type Interventional
Source Tianjin Medical University Cancer Institute and Hospital
Contact Zhi Guo, MD
Phone 18622221211
Email cjr.guozhi@vip.163.com
Status Recruiting
Phase N/A
Start date November 14, 2017
Completion date April 1, 2019

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