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Clinical Trial Summary

This study makes an observation over the objective response rate of autologous erythrocytes derived microparticles packaging methotrexate peritoneal perfusion and systemic therapy combination in the treatment of malignant ascites. All the participants will randomly receive the treatment of autologous erythrocytes derived microparticles packaging methotrexate peritoneal perfusion and systemic therapy combination or convention drugs peritoneal perfusion and systemic therapy combination.


Clinical Trial Description

As a drug carrier, erythrocytes have their own advantages, such as high biocompatibility, high immune compatibility, simple structure and easy access. In this study, microparticles released from erythrocytes are used as the carrier of chemotherapy drugs and effectively kill tumor cells in malignant ascites. These microparticles can easily reach the tumor site and bring the drug into tumor cells, which can overcome the two main problems in normal chemotherapy: damage to normal cells and drug resistance of tumor cells. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03230708
Study type Interventional
Source Hubei Cancer Hospital
Contact Hui ting Xu
Phone 15307176219
Email 2891533@qq.com
Status Recruiting
Phase Phase 1/Phase 2
Start date May 1, 2017
Completion date February 1, 2018

See also
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