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. 2008 Oct;4(5):975–982. doi: 10.2147/tcrm.s3172

Table 1.

A comparison of developing treatments for acute hereditary angioedema attacks in the US

Method of production Mechanism of action Half-life Infusion method FDA status
Berinert P® Plasma concentrate C1-inhibitor 36–48 h iv Pending FDA approval
Cinryze® Plasma concentrate C1-inhibitor 20–92 h iv Pending FDA approval
Rhucin® Recombinant protein C1-inhibitor 3 h iv Was not FDA approved
Ecallantide® Recombinant protein Kallikrein inhibitor 1–4 h Subcutaneous Pending resubmission to the FDA
Icatibant® Synthetic peptide Bradykinin-2 receptor antagonist 1–4 h Subcutaneous Was not approved by the FDA

Abbreviation: h, hours; iv, intravenous.