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Clinical Trial Summary

Hemophagocytic lymphohistiocytosis (HLH) is a rare, poorly recognized and underdiagnosed syndrome of excessive immune activation, which is rapidly fatal. Epstein-Barr virus (EBV) is a common trigger of HLH, particularly in Asian individuals. We aim to analyze metabolomics and cytokine profiles of patients before and after treatment to explore the metabolomic characteristics of EBV-HLH, and search for pathogenic mechanisms and therapeutic targets.


Clinical Trial Description

Hemophagocytic lymphohistiocytosis (HLH) is a rare, poorly recognized and underdiagnosed syndrome of excessive immune activation, which is rapidly fatal. Without early intervention, the median survival time is less than 2 months.Epstein-Barr virus (EBV) is a common trigger of HLH, particularly in Asian individuals. We aim to analyze metabolomics and cytokine profiles of patients before and after treatment to explore the metabolomic characteristics of EBV-HLH, and search for pathogenic mechanisms and therapeutic targets. ;


Study Design


Related Conditions & MeSH terms

  • EBV
  • Hemophagocytic Lymphohistiocytoses
  • Lymphohistiocytosis, Hemophagocytic

NCT number NCT05677178
Study type Observational [Patient Registry]
Source Beijing Friendship Hospital
Contact Zhao Wang, MD
Phone +861083138303
Email wangzhao@ccmu.edu.cn
Status Not yet recruiting
Phase
Start date January 1, 2023
Completion date March 1, 2025

See also
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