Drug intelligence / Profile preview

lanadelumab

Development stage
Approved
Lead developer
Takeda
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Subcutaneous
01

Overview

Lanadelumab is a fully human monoclonal antibody used for the routine prevention of recurrent attacks of hereditary angioedema (HAE) in patients aged 2 years and older. It works by selectively inhibiting plasma kallikrein, a serine protease involved in the generation of bradykinin, which is responsible for the swelling and pain associated with HAE attacks. By blocking plasma kallikrein activity, lanadelumab reduces bradykinin production and helps prevent HAE symptoms. The drug is administered as a subcutaneous injection and provides sustained control over plasma kallikrein activity[1][5][7]. Lanadelumab was developed to address the underlying pathophysiology of HAE related to C1 esterase inhibitor deficiency or dysfunction[6][8].

Brand names
Takhzyro
Other names
lanadelumab-flyo
02

Targets

KLKB1 (Plasma kallikrein)

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