Strong Ph III data on Dyax' HAE drug; submission due in 4th qtr
US drugmaker Dyax Corp has reported positive top-line results from a second late-stage trial of its lead product candidate, DX-88 (ecallantide), for hereditary angioedema. The EDEMA4 trial, conducted under a Special Protocol Assessment granted by the US Food and Drug Administration, achieved statistically-significant improvements among the intent-to-treat population in primary and secondary endpoints.
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