A Long-Term Follow-Up Study in Severe Hemophilia A Subjects Who Received BMN 270 in a Prior BioMarin Clinical Trial (270-401)
Part of paid clinical trials in Los Angeles, California.
- Sponsor
- BioMarin Pharmaceutical
- Study ID
- NCT05768386
- Status
- Enrolling By Invitation
Conditions
- Hemophilia A
Eligibility Criteria
- Sex
- MALE
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Study Details
The BMN 270 clinical development program consists of multiple interventional studies designed to assess the safety and efficacy of a single infusion of BMN 270 for at least 5 years post-infusion. This long-term follow-up study is needed to help further understand the long-term safety of BMN 270 beyond 5 years and to assess the durability of efficacy.
Key Dates
- Start date
- Jan 1, 2023
- Status verified
- Jan 2026
- Primary completion
- Jan 31, 2040
- Completion
- Jan 31, 2040
Study Design
- Enrollment
- 172 participants (estimated)
Primary Outcome Measure
Evaluate the long-term safety of BMN 270 [ Time Frame: Duration of study (10 years) ]
Locations (13)
Find similar trials in Los Angeles, CA
By research site
Orthopedic Institute for Children, Orthopedic Hemophilia Treatment Center· Los Angeles, CAUC Davis Hemophilia Treatment Center· Sacramento, CAUniversity of California San Diego, Hemophilia & Thrombosis Treatment Center· San Diego, CAUniversity of California San Francisco - Moffit Hospital, Outpatient Hematology Clinic· San Francisco, CAUCN Hemophilia and Thrombosis Center· Shandon, CAHemophilia and Thrombosis Center at the University of Colorado Anschutz Medical Campus· Aurora, CO
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