drugset / Trial / NCT00912093

A Study of Icatibant in Patients With Acute Attacks of Hereditary Angioedema (FAST-3)

NCT00912093

Phase 3 Completed 98 enrolled Shire
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study is being conducted to evaluate the efficacy and safety of icatibant compared to placebo in patients experiencing acute attacks of hereditary angioedema (HAE).

Timeline

Start
2009-07-16
Primary completion
2010-10-01
Completion
2010-10-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Icatibant Peptide 30 mg Subcutaneous

Indications