drugset / Trial / NCT00524342

IL-11 in Women With Von Willebrand Disease and Refractory Menorrhagia

NCT00524342

NaSingle-groupOpen-labelPrevention

Summary

The purpose of this study is to determine the efficacy and safety of rhIL-11, when given subcutaneously for six consecutive months, in reducing menstrual blood loss in women with type 1 von Willebrand disease and refractory menorrhagia. Efficacy will be measured by subjective bleeding severity scale and pictorial bleeding chart. Safety will be measured by the frequency of adverse events, including fever, headache, fatigue, myalgias, arthralgias, fluid retention, or edema.

Timeline

Start
2008-01
Primary completion
2010-12
Completion
2010-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Oprelvekin Protein / enzyme biologic 25 ug/kg Subcutaneous