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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

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