drugset / Trial / NCT00097695

Subcutaneous Treatment With Icatibant for Acute Attacks of Hereditary Angioedema

NCT00097695 ↗

Phase 3 Completed 84 enrolled Shire
RandomizedSingle-groupDouble-blindTreatment

Summary

The purpose of this study is to assess the efficacy and safety of Icatibant, a bradykinin antagonist in the treatment of acute cutaneous and/or abdominal attacks in patients with hereditary angioedema (HAE).

Timeline

Start
2004-12-28
Primary completion
2006-07-17
Completion
2006-07-17

Outcome

Missed primary endpoint

paper The primary end point was reached in 2.5 hours with icatibant versus 4.6 hours with placebo in the FAST-1 trial (P=0.14) PMID 20818888 ↗

registry analysis (unspecified test); Randomized -Icatibant vs Randomized -Placebo; p = 0.142; Wilcoxon version of the log-rank test NCT00097695 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Icatibant Peptide 30 mg Subcutaneous

Indications