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  • HAE treatment 'Takhzyro' closer to reimbursement
  • by Eo, Yun-Ho | translator Hong, Ji Yeon | Nov 10, 2025 06:08am
Has passed the Drug Reimbursement Evaluation Committee (DREC) of HIRA after receiving domestic approval in 2021
Demonstrated reduction in the number of HAE attacks through the Phase 3 trial¡¦expected to become the new treatment option
 ¡ã Product photo of Takhzyro (lanadelumab)
A hereditary angioedema (HAE) treatment, 'Takhzyro,' appears closer to insurance reimbursement listing, approximately five years after acquiring domestic approval in South Korea.

Takeda Korea's Takhzyro (lanadelumab) has recently passed the Drug Reimbursement Evaluation Committee (DREC). This is the first achievement since receiving approval from the Ministry of Food and Drug Safety (MFDS) in February 2021.

Attention has been drawn to whether Takhzyro will successfully undergo drug pricing negotiations with the National Health Insurance Service (NHIS) to become a new treatment option for the HAE area, where treatments are lacking.

HAE is a rare disorder caused by dysfunction of the C1-esterase inhibitor (C1
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