The USA’s Institute for Clinical and Economic Review (ICER) yesterday released a Draft Evidence Report assessing the comparative clinical effectiveness and value of therapies for long-term prophylaxis against hereditary angioedema attacks.
The ICER’s report includes four therapies for the prevention of hereditary angioedema attacks including lanadelumab, from Ireland-headquartered Shire (LSE: SHP), which is currently under review by the US Food and Drug Administration with an approval decision expected in August 2018,
The other three, which are already marketed, are: Haegarda (C1 esterase inhibitor human)from CSL Behring, a subsidiary of Australia's CSL Limited (ASX: CSL); Cinryze (C1 esterase inhibitor [human]), also from Shire; and Ruconest (recombinant human C1 inhibitor), from Netherlands-based Pharming (Euronext: PHARM).
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