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KK8005 is an investigational therapeutic being developed by Kyowa Kirin for the treatment of X-linked hypophosphatemia (XLH). XLH is a rare genetic disorder characterized by excessive renal phosphate wasting due to elevated levels of fibroblast growth factor 23 (FGF23), leading to chronic hypophosphatemia and impaired bone mineralization. While Kyowa Kirin previously developed and marketed burosumab (KRN23), a monoclonal antibody targeting FGF23, KK8005 represents a newer addition to their pipeline. It is currently being evaluated in Phase 1/2 clinical trials to assess its safety, tolerability, and pharmacodynamic effects on serum phosphorus levels in adult patients with XLH.
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