Shire adds to evidence base for pricey HAE drug

16 November 2018

Further positive data has been revealed on a drug that has been approved across North America in recent months for hereditary angioedema (HAE).

Ireland-headquartered company Shire (LSE: SHP), which is set to be taken over by Japanese drugmaker Takeda (TYO: 4502) early next year, won approval for Takhzyro (lanadelumab) in the USA in August and in Canada the following month.

The rare disease specialist is presenting further data on the subcutaneously administered treatment’s efficacy and safety in HAE at the American College of Allergy, Asthma & Immunology 2018 Annual Scientific Meeting.

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