Clinical Context

Hereditary angioedema is a rare genetic disorder characterized by recurrent episodes of severe swelling, which can be life-threatening if it affects the airway. The condition is caused by a deficiency or dysfunction of the C1 inhibitor protein, leading to uncontrolled production of bradykinin, a peptide that increases vascular permeability. Current standard treatments include C1 inhibitor replacement therapies and newer medications, such as monoclonal antibodies targeting plasma kallikrein. However, many patients experience breakthrough attacks despite these therapies, highlighting the need for more effective prophylactic options. The approval of donidalorsen aims to address this gap by providing a novel mechanism of action through antisense oligonucleotide therapy targeting prekallikrein, thereby reducing the frequency of angioedema attacks.