drugset / Trial / NCT00456508

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

NCT00456508 ↗

Phase 3 Completed 147 enrolled Shire
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of repeated doses of ecallantide in the treatment of acute attacks of hereditary angioedema and to allow HAE patients continued access to ecallantide. In addition, patients enrolled in DX-88/20 (EDEMA4) trial will be followed up and treated for subsequent attacks in this trial.

Timeline

Start
2007-04-01
Primary completion
2010-06-01
Completion
2010-09-01

Drugs

EvaluationDrugModalityDoseRoute
Subject ecallantide Protein / enzyme biologic 30 mg Subcutaneous

Indications