Overview

Comparison of Outcomes Between Low Dose Emicizumab and Factor VIII in Clinically Severe Hemophilia A

Status:
Recruiting
Trial end date:
2024-06-21
Target enrollment:
0
Participant gender:
Male
Summary
- To outcome between low dose Emicizumab and low dose prophylaxis with FVIII concentration - To study pharmacokinetic, side effect of low dose Emicizumab
Phase:
Phase 2/Phase 3
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Chulalongkorn University
Treatments:
Antibodies, Bispecific
Criteria
Inclusion Criteria:

- Severe or moderate Hemophilia A with baseline FVIII:C of <3 IU/dl or severe bleeding
phenotype

- Receiving low dose FVIII prophylaxis for at least 6 months

Exclusion Criteria:

- Detectable FVIII inhibitor at screening

- Detectable FVIII inhibitor at screening Having other underlying diseases: Juvenile
rheumatoid arthritis, metabolic bone diseases, or other conditions mimicking or
causing joint diseases