RecruitingPHASE2, PHASE3NCT05710692
Study to Evaluate the Safety, PK, PD, and Efficacy of PRX-102 in Japanese Patients With Fabry Disease
Studying Fabry disease
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
- Chiesi Farmaceutici S.p.A.
- Intervention
- PRX-102 1 mg/kg every 2 weeks(drug)
- Enrollment
- 16 enrolled
- Eligibility
- 13-70 years · All sexes
- Timeline
- 2023 – 2029
Study locations (10)
- Fukuoka University Chikushi Hospital, Chikushino-shi, Fukuoka, Japan
- Tohoku University Hospital, Sendai, Miyagi, Japan
- University of the Ryukyu Hospital, Nishihara, Okinawa, Japan
- Osaka University Hospital, Suita, Osaka, Japan
- Juntendo University Hospital, 3-1-3 Hongo, Bunkyo-ku, Tokyo, Bunkyo-ku, Tokyo, Japan
- Tokyo Jikei University Hospital, Minato-ku, Tokyo, Japan
- Keio University Hospital, Shinjuku-ku, Tokyo, Japan
- Asahikawa Medical University Hospital, Asahikawa, Japan
- Niigata University Medical & Dental Hospital, Niigata, Japan
- National Hospital Organization Okayama Medical Center, Okayama, Japan
Collaborators
ICON plc
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.
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