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Thursday, May 17, 2018

Ultragenyx Phase 3 study meets primary endpoints

Ultragenyx Pharmaceutical announced that the Phase 3 study of Crysvita met its primary endpoint demonstrating that Crysvita was superior to oral phosphate and active vitamin D in improving rickets in children with X-linked hypophosphatemia, or XLH, after 40 weeks of treatment. The study also showed improvement in important metabolic and functional measures with Crysvita treatment, and a safety profile similar to that observed in other Crysvita pediatric XLH studies. Crysvita is an antibody that blocks fibroblast growth factor 23, or FGF23, a hormone that causes phosphate urinary excretion and suppresses active vitamin D production by the kidney.

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