CompletedPhase 2NCT02456038
Safety and Efficacy of Asfotase Alfa in Patients With Hypophosphatasia (HPP)
Studying Hypophosphatasia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Translational Research Center for Medical Innovation, Kobe, Hyogo, Japan
- Principal Investigator
- Keiichi OzonoOsaka University Hospital
- Intervention
- Asfotase Alfa (ALXN1215)(drug)
- Enrollment
- 13 target
- Eligibility
- All sexes
- Timeline
- 2014 – 2015
Study locations (12)
- Kurume University Hospital, Kurume, Fukuoka, Japan
- National Hospital Organization Nagara Medical Center, Gifu, Gifu, Japan
- Hiroshima University Hospital, Hiroshima, Hiroshima, Japan
- Hokkaido University Hospital, Sapporo, Hokkaido-prefecture, Japan
- Tohoku University Hospital, Sendai, Miyagi, Japan
- Niigata University Medical & Dental Hospital, Niigata, Niigata, Japan
- Osaka Medical Center and Research Institute for Maternal and Child Health, Izumi, Osaka, Japan
- Osaka University Hospital, Suita, Osaka, Japan
- Saitama Children's Medical Center, Saitama, Saitama, Japan
- Hamamatsu University Hospital, Hamamatsu, Shizuoka, Japan
- Nippon Medical School Hospital, Bunkyo-ku, Tokyo, Japan
- Showa General Hospital, Kodaira, Tokyo, Japan
Collaborators
Osaka University Graduate School of Medicine
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT02456038 on ClinicalTrials.govOther trials for Hypophosphatasia
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