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The primary objective of this study is to assess the safety and tolerability of KRN23 after a single intravenous (IV) and subcutaneous (SC) administration in XLH patients.
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Lead Sponsor
Kyowa Kirin Co., Ltd.
Collaborators
NCT03745521 · X-Linked Hypophosphatemia
NCT03775187 · X-linked Hypophosphatemia, Tumor-Induced Osteomalacia
NCT04188964 · X-linked Hypophosphatemia (XLH)
NCT02915705 · X-Linked Hypophosphatemia
NCT04842032 · X-linked Hypophosphatemia (XLH)
Yale University School of Medicine
New Haven, Connecticut
General Clinical Research Center, Indiana University School of Medicine
Indianapolis, Indiana
Duke Clinical Research Unit
Durham, North Carolina
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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