Registry for Patients With X-Linked Hypophosphatemia
NCT03193476 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 1343
Last updated 2024-09-19
Summary
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.
Conditions
- X-Linked Hypophosphatemia
Sponsors & Collaborators
-
Iqvia Pty Ltd
collaborator INDUSTRY -
Kyowa Kirin Pharmaceutical Development Ltd
lead INDUSTRY
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-09-12
- Primary Completion
- 2029-02-01
- Completion
- 2029-07-01
Countries
- Belgium
- Bulgaria
- Czechia
- Denmark
- France
- Germany
- Hungary
- Ireland
- Israel
- Italy
- Latvia
- Netherlands
- Norway
- Portugal
- Slovakia
- Slovenia
- Spain
- Sweden
- Switzerland
- United Kingdom
Study Locations
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