Clinical Trials Logo

Clinical Trial Summary

The purpose of this study is to investigate efficacy and safety of Chidamide Combined With Cyclophosphamide,Prednisone,Thalidomide in Treatment of Fragile Patients With Relapse/Refratory Peripheral T Cell Lymphoma :a Phase II,Single-arm,Open-label, Muti-center Study


Clinical Trial Description

Chidamide is a new histone deacetylase inhibitor and shows anti-tumor activity in Relapse/Refratory Peripheral T Cell Lymphoma.Cyclophosphamide,Prednisone,Thalidomide(CPT) is an oral combination regimen for lymphoma patients who can not stand the standard chemotherapy. The investigators therefore design this open-label,phase II, single-arm trial to investigate the efficacy of Chidamide Combined With CPT in treatment of fragile Patients With Relapse/Refratory Peripheral T Cell Lymphoma

Primary Outcome Measures:

• overall response rate

Secondary Outcome Measures:

- duration of response

- progression free survival

- overall survival Enrollment:45 Study Start Date: August 2016 Primary Completion Date: March 2018 ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02879526
Study type Interventional
Source The First Affiliated Hospital with Nanjing Medical University
Contact Huayuan Zhu, M.D., Ph.D.
Phone 86 25 6813 6034
Email huayuan.zhu@hotmail.com
Status Recruiting
Phase Phase 2
Start date August 2016
Completion date August 2019