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Tadekinig alfa is a recombinant human interleukin-18 (IL-18) binding protein that acts by specifically binding to and neutralizing IL-18, a pro-inflammatory cytokine implicated in several rare systemic inflammatory conditions. By restoring the balance between IL-18 and its natural inhibitor, Tadekinig alfa reduces pathological inflammation associated with diseases such as macrophage activation syndrome (MAS), hemophagocytic lymphohistiocytosis (HLH), NLRC4-macrophage activation syndrome (NLRC4-MAS), XIAP deficiency, adult-onset Still's disease (AoSD), and systemic juvenile idiopathic arthritis (sJIA). The drug is administered subcutaneously and has demonstrated favorable safety and efficacy profiles in clinical trials. Tadekinig alfa has received orphan drug designations in both the US and Europe for these indications[1][3][5][6][7].
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