drugset / Trial / NCT00262080

Efficacy and Safety Study of DX-88 to Treat Acute Attacks of Hereditary Angioedema (HAE)

NCT00262080 ↗

Phase 3 Completed 91 enrolled Shire
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to determine if a subcutaneous dose of DX-88 (ecallantide; an investigational product) is safe and relieves symptoms of HAE in patients suffering from moderate to severe acute attacks of HAE.

Timeline

Start
2005-12-31
Primary completion
2005-12-31
Completion
2007-02-28

Outcome

Met primary endpoint

registry analysis (unspecified test); Ecallantide vs Placebo; p = 0.037; non-parametric Wilcoxon Rank Sum test NCT00262080 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject ecallantide Protein / enzyme biologic 30 mg Subcutaneous

Indications