Current issues in Hereditary Angioedema (HAE) - Ipopi
Current issues in Hereditary Angioedema (HAE) - Ipopi
Current issues in Hereditary Angioedema (HAE) - Ipopi
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Treatment of C1 <strong>in</strong>hibitor deficiency<br />
-ecallantide (DX88; Kalbitor)<br />
• Effectıve<br />
• Subcutaneous<br />
– Kallikre<strong>in</strong> <strong>in</strong>hibitor<br />
– Produced <strong>in</strong> pichia pastoris (recomb<strong>in</strong>ant<br />
prote<strong>in</strong>)<br />
• Short half life<br />
– 2 hours<br />
Avaılable ın USA