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Other News To Note

Tuesday, November 15, 2011
Dyax Corp., of Cambridge, Mass., said it has decided with partner Sigma-Tau Group, of Rome, to withdraw the European marketing authorization application for hereditary angioedema drug Kalbitor (ecallantide). Although Kalbitor is approved in the U.S., European regulators indicated the data were not sufficient to prove a positive risk-benefit.

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