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Study identifier: NCT05710692 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Study to Evaluate the Safety, PK, PD, and Efficacy of PRX-102 in Japanese Patients With Fabry Disease

Condition: Fabry Disease  ·  Sponsor: Chiesi Farmaceutici S.p.A.

PhasePhase 2/Phase 3
Planned participants16
Who can joinAll sexes, 13 Years to 70 Years
Healthy volunteersNo

About this study

The aim of this study is to evaluate the safety and efficacy of pegunigalsidase alfa in Japanese patients (adults and adolescents) affected by Fabry disease. It is planned of a total of approximately 16 male and female Fabry disease patients between the ages of 13 and 70 years to be part of the study. The study is conducted in Japan.

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

Talk to the study team

Chiesi Clinical Trial  ·  +3905212791  ·  clinicaltrials_info@chiesi.com

Always discuss trial participation with your own doctor first.

Locations (10)

Fukuoka University Chikushi HospitalChikushino-shi, Fukuoka, JapanWithdrawn
Tohoku University HospitalSendai, Miyagi, JapanRecruiting
University of the Ryukyu HospitalNishihara, Okinawa, JapanRecruiting
Osaka University HospitalSuita, Osaka, JapanRecruiting
Juntendo University Hospital, 3-1-3 Hongo, Bunkyo-ku, TokyoBunkyo-ku, Tokyo, JapanRecruiting
Tokyo Jikei University HospitalMinato-ku, Tokyo, JapanRecruiting
Keio University HospitalShinjuku-ku, Tokyo, JapanRecruiting
Asahikawa Medical University HospitalAsahikawa, JapanRecruiting
Niigata University Medical & Dental HospitalNiigata, JapanRecruiting
National Hospital Organization Okayama Medical CenterOkayama, JapanNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT05710692