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Study identifier: NCT06202027 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Post Marketing Surveillance Study to Observe Safety and Effectiveness of CRYSVITA® in S. Korean Patients

Condition: FGF23-related Hypophosphataemic Rickets and Osteomalacia  ·  Sponsor: Kyowa Kirin Korea Co., Ltd.

PhaseN/A
Planned participants100
Who can joinAll sexes, 1 Day to no upper limit
Healthy volunteersNo

About this study

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

This description comes directly from the study's public registry record.

Talk to the study team

HaeMi Park  ·  +82-10-3378-3471  ·  haemi.park.m8@kyowakirin.com

Always discuss trial participation with your own doctor first.

Locations (13)

Wonju Severance Christian HospitalWŏnju, Gangwon-do, South KoreaRecruiting
Ajou University HospitalSuwon, Gyeonggi-do, South KoreaRecruiting
Yangsan Pusan National University HospitalYangsan, Gyeongsangnam-do, South KoreaRecruiting
Chonnam National University HospitalGwangju, Jeollanam-do, South KoreaRecruiting
Chungnam National University Sejong HospitalSejong, Sejong Special Self-Governing City, South KoreaRecruiting
Inje University Busan Paik HospitalBusan, South KoreaRecruiting
Pusan National University HospitalBusan, South KoreaRecruiting
Seoul National University HospitalSeoul, South KoreaRecruiting
Seoul National University HospitalSeoul, South KoreaRecruiting
Seoul National University HospitalSeoul, South KoreaRecruiting
Severance HospitalSeoul, South KoreaRecruiting
Severance HospitalSeoul, South KoreaRecruiting

+ 1 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06202027