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Clinical Trial Summary

This is a single arm, open, single-center clinical study. The patients who are diagnosed with lymphoma and intend to undergo ASCT will be enrolled. The aim of this study is to investigate the efficacy and safety of the conditioning regimen using mitoxantrone hydrochloride liposome, BCNU, etoposide and cytarabine for ASCT.


Clinical Trial Description

High-dose chemotherapy combined with autologous hematopoietic stem cell transplantation (ASCT) is considered the standard of care for patients with chemotherapy-sensitive relapsed/refractory (R/R) non-Hodgkin's lymphoma (NHL). BEAM regimen is the most commonly used conditioning regimen for ASCT in lymphoma. But its application is limited by the adverse drug reactions. This present project is a one-arm, open, single-center clinical study. It aims to evaluate the efficacy and safety of mitoxantrone hydrochloride liposome, carmostine, etoposide, and cytarabine as the conditioning regimen for ASCT in patients with lymphoma. ;


Study Design


Related Conditions & MeSH terms

  • Autologous Hematopoietic Stem Cell Transplantation
  • Lymphoma

NCT number NCT05681403
Study type Interventional
Source First Affiliated Hospital Xi'an Jiaotong University
Contact Pengcheng He, MD
Phone 0086-029-85324035
Email hepc@163.com
Status Not yet recruiting
Phase N/A
Start date January 15, 2023
Completion date December 31, 2026

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