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May 15, 2026

Kyowa Kirin secures FDA approval for Crysvita dosing update

Kyowa Kirin has received approval from the US Food and Drug Administration (FDA) for a dosing update to the prescribing information for Crysvita (burosumab-twza), introducing a new option for adults with X-linked hypophosphataemia (XLH).

The recombinant, fully human monoclonal IgG1 antibody targets fibroblast growth factor 23 in XLH. Credit: Michele Ursi / Shutterstock.com.