Post Marketing Surveillance Study to Observe Safety and Effectiveness of CRYSVITA® in S. Korean Patients
NCT06202027 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 100
Last updated 2025-08-29
Summary
The objective of this post-marketing surveillance (PMS) study is to assess the safety and effectiveness of CRYSVITA injection 10, 20, and 30mg, equivalent to in routine clinical settings
Conditions
- FGF23-related Hypophosphataemic Rickets and Osteomalacia
Interventions
- DRUG
-
FGF23-related hypophosphataemic rickets and osteomalacia
FGF23-related hypophosphataemic rickets and osteomalacia
Sponsors & Collaborators
-
Kyowa Kirin Korea Co., Ltd.
lead INDUSTRY
Principal Investigators
-
HaeMi Park · Kyowa Kirin Korea Co., Ltd.
Eligibility
- Min Age
- 1 Day
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2023-08-11
- Primary Completion
- 2031-06-16
- Completion
- 2031-07-16
Countries
- South Korea
Study Locations
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