Legal status In December 2024, the
Committee for Medicinal Products for Human Use of the
European Medicines Agency adopted a positive opinion, recommending the granting of a marketing authorization for the medicinal product Andembry, intended for the prevention of recurrent attacks of hereditary angioedema. Garadacimab was designated an orphan medicine by the EMA. Garadacimab was approved for medical use in the United States in June 2025.
Names Garadacimab is the
international nonproprietary name. Garadacimab is sold under the brand name Andembry. == References ==