Shire notches up second approval for Takhzyro

20 September 2018

Following US approval last month, soon-to-be Takeda Pharmaceutical (TYO: 4502) acquisition Shire (LSE: SHP) has now also been granted authorization in Canada for Takhzyro (lanadelumab), as a treatment for hereditary angioedema (HAE).

The approval means the therapy may now be marketed for routine prevention of attacks of the rare and debilitating genetic disorder in adolescents and adults.

Takhzyro is a fully- human monoclonal antibody, given through injection. Patients can self-administer the therapy every two or four weeks.

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