Prevalence of Inhibitor Development in Hemophilia A Patients Receiving Coageight: A Multicenter Cross-sectional Observational Study
NCT07791836 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 262
Last updated 2026-08-28
Summary
This is a cross-sectional, observational, multi-center study to assess the prevalence of inhibitor development in hemophilia A patients receiving Coageight (rFVIII-Fc, AryoGen Pharmed Co.).
Conditions
Interventions
- DRUG
-
efmoroctocog alfa
This study assesses patients with a history of at least 10 exposure days (EDs) to recombinant factor VIII with Fc fusion (Coageight) within the 12 months prior to enrollment.
Sponsors & Collaborators
-
AryoGen Pharmed Co.
lead INDUSTRY
Eligibility
- Min Age
- 2 Years
- Sex
- MALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-08-23
- Primary Completion
- 2027-02-20
- Completion
- 2027-02-20
Countries
- Iran
Study Locations
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