Status: Recruiting
Registry for Patients With X-Linked Hypophosphatemia
This is an international, multicentre, prospective, non-interventional, observational Registry of patients with X-Linked hypophosphatemia (XLH). The main objective of this XLH Registry is to collect data to characterise the treatment, progression and long-term outcomes of XLH in both adult and paediatric settings.
Participants needed: 1,343
Trial details
Biological sex: AllType: ObservationalSponsor: Kyowa Kirin Pharmaceutical Development LtdUpdated: Sep 19, 2024Locations: 118Duration: 10 Years
Eligibility criteria
Patients aged from ≥0 years of age at baseline [+2]
Patient or their legally designated representative does not have the cognitive c... [+2]