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X-linked Hypophosphatemia (XLH)
Clinical trial pipeline · Data from ClinicalTrials.gov
See which X-linked Hypophosphatemia (XLH) trials may be worth asking aboutClinical trial pipeline · Data from ClinicalTrials.gov
See which X-linked Hypophosphatemia (XLH) trials may be worth asking aboutNorth America
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X-linked hypophosphataemia (XLH) is a rare, hereditary condition. The genetic defect leads to low blood phosphate levels and vitamin D suppression. Phosphate is…
A first-in-human study of KK8123 in adults with X-linked hypophosphatemia.
This is an international, multicentre, prospective, non-interventional, observational Registry of patients with X-Linked hypophosphatemia (XLH). The main object…
The goal of this National Registry is to is to collect information from patients with rare kidney diseases, so that it that can be used for research. The purpo…
MOSAIC aims to determine whether oro-dental morphological anomalies, particularly palatal morphology, associated with rare bone and cartilage diseases can be pr…
The purpose of this study is to better understand how X-linked hypophosphatemia (XLH) affects the body and daily life. Phosphate levels are critical in managing…