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Burosumab in X-linked hypophosphatemia: a profile of its use in the USA
Burosumab (Crysvita(®)), a fully human IgG1 monoclonal antibody directed at fibroblast growth factor 23 (FGF23), is indicated for the treatment of X-linked hypophosphatemia (XLH), a condition associated with excessive FGF23 production. It directly addresses the excessive FGF23 activity in patients w...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer International Publishing
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6223702/ https://www.ncbi.nlm.nih.gov/pubmed/30459508 http://dx.doi.org/10.1007/s40267-018-0560-9 |
Sumario: | Burosumab (Crysvita(®)), a fully human IgG1 monoclonal antibody directed at fibroblast growth factor 23 (FGF23), is indicated for the treatment of X-linked hypophosphatemia (XLH), a condition associated with excessive FGF23 production. It directly addresses the excessive FGF23 activity in patients with XLH by binding to FGF23, and inhibiting its signaling. This leads to increased gastrointestinal phosphate absorption and renal phosphate reabsorption, thereby improving serum phosphate levels, and, ultimately, bone mineralization and the risk of bone disease. In clinical trials, subcutaneous burosumab increased serum phosphorus levels in pediatric and adult patients with XLH, as well as significantly improving the severity of rickets in children, and improving pain, stiffness, physical functioning, and fracture/pseudofracture healing in adults. Burosumab is well tolerated by children and adults with XLH, with most treatment-emergent adverse events being of mild to moderate severity. |
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