New hope for kids with rare bone disease: testing Next-Generation treatment
NCT ID NCT06079372
Summary
This study is testing a new drug called ALXN1850 against the current standard treatment (asfotase alfa) in children aged 2 to under 12 who have a rare bone-weakening condition called hypophosphatasia (HPP). The main goal is to see if the new drug is as safe and well-tolerated as the standard one. Researchers will also check if it helps improve bone health, walking ability, and motor skills.
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Contacts and locations
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Locations
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Research Site
Hartford, Connecticut, 06106, United States
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Baltimore, Maryland, 21287, United States
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Minneapolis, Minnesota, 55455, United States
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Kansas City, Missouri, 64108, United States
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Durham, North Carolina, 27705, United States
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Nashville, Tennessee, 37212, United States
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Mar del Plata, B7600, Argentina
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South Brisbane, 4101, Australia
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Ottawa, Ontario, K1H 8L1, Canada
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Bunkyō City, 113-8431, Japan
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Minatoku, 105-8471, Japan
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Suita-shi, 565-0871, Japan
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Yonago-shi, 683-8504, Japan
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Altındağ, 06230, Turkey (Türkiye)
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Ankara, 06560, Turkey (Türkiye)
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Edirne, 22030, Turkey (Türkiye)
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Erzurum, 25240, Turkey (Türkiye)
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Istanbul, 34899, Turkey (Türkiye)
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Birmingham, B4 6NH, United Kingdom
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Manchester, United Kingdom
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Sheffield, S10 2TH, United Kingdom
Conditions
Explore the condition pages connected to this study.