RecruitingPhase 3NCT07080905
Phase 3, Open-label, Single-dose Study of CSL222 in Adolescent Male Subjects (≥ 12 to < 18 Years of Age) With Severe or Moderately Severe Hemophilia B
Studying Hemophilia B
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
- CSL Behring
- Principal Investigator
- Study DirectorCSL Behring
- Intervention
- CSL222 (Adeno-associated viral vector serotype 5 [AAV5]-hFIXco-Padua)(genetic)
- Enrollment
- 20 enrolled
- Eligibility
- MALE
- Timeline
- 2025 – 2033
Study locations (8)
- Center for Inherited Blood Disorders, Orange, California, United States
- University of Florida, Gainesville, Florida, United States
- Arthur M. Blank Hospital - Children's Healthcare of Atlanta, Atlanta, Georgia, United States
- University of Michigan Medical Center, Ann Arbor, Michigan, United States
- St. Jude Children's Research Hospital, Memphis, Tennessee, United States
- Chaim Sheba Medical Center, Ramat Gan, Israel
- St Thomas Hospital, London, United Kingdom
- John Radcliffe Hospital - Oxford University Hospitals NHS, Oxford, United Kingdom
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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