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Dyax shares score on HAE drug 'breakthrough' status

This article was originally published in Scrip

Executive Summary

Shares of Dyax jumped about 5% in morning trading on 7 July on word the FDA had granted breakthrough therapy designation (BTD) – a mechanism intended to help expedite the regulatory process for medicines aimed at treating serious conditions – for the company's investigational hereditary angioedema (HAE) drug of DX-2930, a fully human monoclonal antibody inhibitor of plasma kallikrein (pKal).

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This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

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