Active, not recruitingPhase 3NCT06224907
Phase 3 Study for Efficacy and Safety Outcomes Data in Japanese Patients With Severe Hemophilia A
Studying Severe hemophilia A
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
- BioMarin Pharmaceutical
- Principal Investigator
- Medical Monitor, MDBioMarin Pharmaceutical
- Intervention
- Valoctocogene roxaparvovec(biological)
- Enrollment
- 6 target
- Eligibility
- 18 years · MALE
- Timeline
- 2023 – 2029
Study locations (4)
- Asahikawa Medical University Hospital, Hokkaido, Asahikawa, Japan
- Saitama Medical University Hospital, Saitama, Iruma-gun, Japan
- Nagoya University Hospital, Aichi, Nagoya, Japan
- Tokyo Medical University Hospital, Tokyo, Shinjuku-ku, Japan
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 NCT06224907 on ClinicalTrials.govOther trials for Severe hemophilia A
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