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)

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