drugset / Trial / NCT00358501

Defibrotide for the Treatment of Severe Hepatic Veno-Occlusive Disease in Hematopoetic Stem Cell Transplant Patients

NCT00358501 ↗

Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to (1) demonstrate the efficacy and safety (toxicity) of 25 mg/kg/day of Defibrotide in patients with severe veno-occlusive disease (sVOD) and (2) evaluate serum and endothelial markers of veno-occlusive disease (VOD) through the analysis of blood samples.

Timeline

Start
2006-07
Primary completion
2008-09
Completion
2015-03

Outcome

Met primary endpoint

paper observed rates equaled 38.2% in the defibrotide group and 25% in the controls (23% estimated difference; 95.1% confidence interval [CI], 5.2-40.8;P= .0109 PMID 26825712 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Defibrotide Oligonucleotide (other) 6.25 mg/kg Intravenous