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An Investigator-sponsored study on rFVIIa prophylaxis in children with haemophilia A and inhibitors - ENJOIH 01

Conditions
Haemophilia A
MedDRA version: 12.1Level: LLTClassification code 10056492Term: Haemophilia A with anti factor VIII
Registration Number
EUCTR2009-010172-21-IT
Lead Sponsor
Dott.ssa Elena Santagostino
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
Male
Target Recruitment
50
Inclusion Criteria

Male patients with haemophilia A who have been treated with factor VIII on demand or on prophylaxis and who have developed inhibitors to factor VIII. Age < 8 years. ≤ 2 years from the time of first inhibitor detection. High-responding inhibitors (historical peak > 5 BU/mL) and known anamnestic response in case of negative inhibitor titre. Candidates to start ITI. Maximal two bleedings in the same joint within the last 6 months before entering the study or maximal six joint bleeds in the same joint within 2 years. Adequate venous access for daily infusion and capable (patient or caregiver) of reconstituting and injecting the study drug (as judged by the Investigator). Informed consent by parents or legal guardians.
Are the trial subjects under 18? yes
Number of subjects for this age range:
F.1.2 Adults (18-64 years) no
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

ITI already started. Known or suspected hypersensitivity to the active substance or any of the excipients of the study drug, or to mouse, hamster or bovin protein... Administration of any investigational product within 30 days prior to randomisation. Other coagulation disorders than congenital haemophilia A. Family history of thrombosis at an early age (< 40 years), known thrombophilia, any previous thrombosis including catheter-related deep vein thrombosis, previous neonatal thrombosis. Known pseudo tumours. Known severe liver disease. Platelet count < 50,000 platelets/?L at screening. Surgery within one month or planned major and/or orthopaedic surgery.

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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