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Clinical Trial Summary

Hemophagocytic syndrome (HS) is a rare condition that can be responsible for severe organ failure. Therapeutic guidelines are mainly based on observational studies and expert opinions: no therapeutic advance has been developed for years, explaining why mortality in HS remains high (Intensive Care Unit mortality ranging from 40 to 70%). If etoposide remains the gold standard in critically ill HS patients, nearly 20% of patients are refractory to this therapy: treatment escalation is common, most often requiring the administration of intensive treatments generating high toxicity. Ruxolitinib is the first approved JAK inhibitor. It has been associated with improvement of HS manifestations and survival in a pre-clinical murine model. Data in humans are scarce but promising. The aim is to demonstrate that ruxolitinib, in association with standard of care, may reverse organ failure (as represented by Sequential Organ Failure Assessment (SOFA) score) better than standard of care alone in critically ill patients with acquired HS.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Lymphohistiocytosis, Hemophagocytic
  • Syndrome

NCT number NCT06244862
Study type Interventional
Source Assistance Publique - Hôpitaux de Paris
Contact Sandrine Valade, Dr
Phone +33142499419
Email sandrine.valade@aphp.fr
Status Not yet recruiting
Phase Phase 2
Start date February 1, 2024
Completion date February 1, 2026