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  • Ultomiris, a successor to Soliris, was approved in Korea
  • by Lee, Tak-Sun | translator Choi HeeYoung | May 27, 2020 06:04am
It is administered once every 8 weeks as the number of administrations is shorter than that of a comparative drug
Handok acquired a domestic item license for paroxysmal nocturnal hemoglobinuria (PNH) treatment 'Ultomiris'. Ultomiris is a product that was expected as a successor to Soliris, and is a drug developed by Alexion, like Soliris.

In particular, it has attracted attention in that it has increased convenience by significantly reducing the number of doses than Soliris.

On the 21st, the MFDS approved a license for Ultomiris (Ravulizumab) by Handok as a treatment for paroxysmal nocturnal hemoglobinuria (PNH) in adults on the 21st.

Ultomiris is a drug approved by the U.S. Food and Drug Administration (FDA) in December 2018 and the European Medicines Agency (EMA) in July 2018. In Korea, a phase III clinical trial has b
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