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Hereditary Angioedema

Company announces results from two clinical trials of DX-88

Published in Hepatitis Weekly, August 1st, 2005

Dyax Corp. (DYAX) announced positive top-line results from its completed phase I trial to evaluate safety and pharmacokinetics (PK) of subcutaneously administered DX-88 in normal volunteers.

The company also announced the presentation at the World Allergy Congress in Munich, Germany of positive interim results from the first 120 attacks of hereditary angioedema (HAE) treated with intravenously administered DX-88 in its open-label, repeat-dosing, phase II trial referred to as EDEMA2. DX-88 is being developed in a joint venture with Genzyme Corp. for the treatment of HAE, a debilitating and life-threatening inflammatory condition characterized by unpredictable attacks of...

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