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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
A First-in-human Study of KK8123 in Adults With X-linked HypophosphatemiaBone Diseases, Metabolic, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Hypophosphatemia, Familial, Male Urogenital Diseases, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Rare Diseases, Rickets, X-Linked Hypophosphatemic, Urogenital Diseases, X-linked hypophosphatemic rickets, bone disorder, calcium metabolic disease, hereditary disease, hypophosphatemia, hypophosphatemic rickets, inborn errors of metabolism, inborn metal metabolism disorder, kidney disorder, metabolic disease, musculoskeletal system disorder, nutritional deficiency disease, nutritional disorder, phosphorus metabolism disease, renal tubular transport disease, rickets, urinary system disorder, vitamin D deficiency, vitamin deficiency disorderRecruitingPhase 1 / Phase 22026-09-21NCT06525636

2 results · Page 1 of 1

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OrganizationsLinked trials
Kyowa Kirin Co., Ltd.15
Kyowa Kirin, Inc.6

10 results · Page 1 of 1

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Research sitesCityCountryLinked trials
Bone Research and Education CenterOakvilleCanada1
Hoptial BictreLe Kremlin-BicêtreFrance1
Hospital Universitario La PazMadridSpain217
Indiana University School of Medicine University HospitalIndianapolisUnited States1
Institute of Osteology and Biomechanics (IOBM)HamburgGermany1
Mayo ClinicRochesterUnited States664
Universitaetsklinikum WurzburgWürzburgGermany1
University of California - San FranciscoSan FranciscoUnited States4
Vanderbilt University Medical CenterNashvilleUnited States427
Yale Center for XLH/ Yale University School of MedicineNew HavenUnited States1