Last updated on November 2018

Study of Longitudinal Observation for Patient With X-linked Hypophosphatemic Rickets/Osteomalacia in Collaboration With Asian Partners

Are you eligible to participate in this study?

You may be eligible for this study if you meet the following criteria:

  • Conditions: Familial Hypophosphatemic Rickets
  • Age: - 100 Years
  • Gender: Male or Female

Inclusion Criteria:

  • Patients must meet at least one of the following:
    1. Documented PHEX gene mutation
    2. Documented PHEX gene mutation in at least one family member with X-linked genetic relationship
    3. Documented FGF23 >30 pg/mL
  • Typical clinical findings of rickets/osteomalacia
  • Written informed consent obtained from patients aged >=20 years or from parents or legally acceptable representatives of patients aged <20 years

Exclusion Criteria:

  • Participation in any clinical study (trial) at the time of informed consent
  • Any patient whose participation in the study is considered inappropriate by the investigator or the subinvestigator

Recruitment Status: Open

Brief Description Eligibility Contact Research Team

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