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

Outcome

Met primary endpoint

paper icatibant significantly reduced median times (vs placebo) to 50% or more reduction in symptom severity (2.0 vs 19.8 hours; P < .001, primary endpoint) PMID 22123383 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Icatibant Peptide 30 mg Subcutaneous

Indications