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Burosumab vs conventional therapy in children with X-linked hypophosphatemia: results of the open-label, phase 3 extension period
Department of Pediatrics, Faculty of Medicine, University of Ottawa, Ottawa Ontario, Canada.
Department of Paediatrics and Adolescent Medicine, Johannes Kepler University Linz, Linz, Austria; Institute of Metabolism and Systems Research, University of Birmingham, Edgbaston, Birmingham, United Kingdom.
Department of Surgery, Pediatrics, and Human Genetics, Shriners Hospitals for Children and McGill University, Montreal Quebec, Canada.
Department of Pediatrics, University of California, San Francisco CA, United States.
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2024 (English)In: JBMR Plus, E-ISSN 2473-4039, Vol. 8, no 1, article id ziad001Article in journal (Refereed) Published
Abstract [en]

In a randomized, open-label phase 3 study of 61 children aged 1-12 years old with X-linked hypophosphatemia (XLH) previously treated with conventional therapy, changing to burosumab every 2 weeks (Q2W) for 64 weeks improved the phosphate metabolism, radiographic rickets, and growth compared with conventional therapy. In this open-label extension period (weeks 64-88), 21 children continued burosumab Q2W at the previous dose or crossed over from conventional therapy to burosumab starting at 0.8 mg/kg Q2W with continued clinical radiographic assessments through week 88. Efficacy endpoints and safety observations were summarized descriptively for both groups (burosumab continuation, n = 6; crossover, n = 15). At week 88 compared with baseline, improvements in the following outcomes were observed in the burosumab continuation and crossover groups, respectively: mean (SD) RGI-C rickets total score (primary outcome), +2.11 (0.27) and +1.89 (0.35); mean (SD) RGI-C lower limb deformity score, +1.61 (0.91) and +0.73 (0.82); and mean (SD) height Z-score + 0.41 (0.50) and +0.08 (0.34). Phosphate metabolism normalized rapidly in the crossover group and persisted in the continuation group. Mean (SD) serum alkaline phosphatase decreased from 169% (43%) of the upper limit of normal (ULN) at baseline to 126% (51%) at week 88 in the continuation group and from 157% (33%) of the ULN at baseline to 111% (23%) at week 88 in the crossover group. During the extension period, treatment-emergent adverse events (AEs) were reported in all 6 children in the burosumab continuation group and 14/15 children in the crossover group. The AE profiles in the randomized and extension periods were similar, with no new safety signals identified. Improvements from baseline in radiographic rickets continued in the extension period among children with XLH who remained on burosumab. Children who crossed over from conventional therapy to burosumab demonstrated a rapid improvement in phosphate metabolism and improved rickets healing over the ensuing 22 weeks.

Place, publisher, year, edition, pages
Oxford University Press, 2024. Vol. 8, no 1, article id ziad001
Keywords [en]
burosumab, FGF23, phosphate, rare disease, x-linked hypophosphatemia
National Category
Endocrinology and Diabetes
Identifiers
URN: urn:nbn:se:oru:diva-113457DOI: 10.1093/jbmrpl/ziad001ISI: 001203133400006PubMedID: 38690124Scopus ID: 2-s2.0-85193424229OAI: oai:DiVA.org:oru-113457DiVA, id: diva2:1855338
Note

This study was sponsored and funded by Ultragenyx Pharmaceutical Inc. in partnership with Kyowa Kirin International plc. Medical writing support was provided by Ben Scott, PhD (Scott Medical Communications, LLC) and was funded by Ultragenyx Pharmaceutical Inc. Additional editorial support was provided by Jamie Ziobro, an employee and share holder of Ultragenyx Pharmaceutical Inc. At Indiana University, the research was done at the Indiana Clinical and Translational Sciences Institute, funded in part by UL1TR002529 from the National Institutes of Health, National Center for Advancing Translational Sciences, Clinical, and Translational Sciences Award. In Montreal and St. Louis, the work was also supported by the Shriners of North America. Dr. Ward is supported by a Tier 1 (Senior) Research Chair in Pediatric Bone Disorders from the University of Ottawa and Children's Hospital of Eastern Ontario Research Institute. 

Available from: 2024-04-30 Created: 2024-04-30 Last updated: 2025-01-20Bibliographically approved

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