Safety and Efficacy of BAY94-9027 in Previously Treated Male Children With Haemophilia A

Bayer

Status and phase: Completed; Phase 3

Conditions: Hemophilia A

Treatments: Biological: BAY94-9027

Study type: Interventional

Funder types: Industry

Identifiers

NCT01775618

2012-004434-42 (EudraCT Number)

15912

Details and patient eligibility

About

Hemophilia A is an inherited blood disorder in which one protein, Factor VIII, needed to form blood clots is missing or not present in sufficient levels. Hemophilia A causes the clotting process to be slowed and the person experiences bleeds causing serious problems that could lead to disability. The current standard treatment for severe hemophilia A is infusion of FVIII to stop bleeding, or regular scheduled treatment to prevent bleeds from occuring. Due to the short half-life of FVIII, prophylaxis may require treatment as often as every other day.

In this trial safety and efficacy of a long-acting recombinant Factor VIII molecule is being evaluated in 50 male subjects, < 12 years of age, with severe Hemophilia A. These subjects will receive open label treatment with long-acting rFVIII for approximately 6 months (or longer until 50 exposure days) on a regular schedule at least once every 7-days. Doses and dose intervals may be adapted to the subject's clinical need. A second group of patients will receive open label treatment with the same drug for 12 weeks on a regular schedule of 2x/week. Patients will attend the treatment center for routine blood samples and will be required to keep an electronic diary.

Subjects will be offered participation in an optional extension study to collect observations for at least an additional 50 exposure days.

Enrollment: 73 patients

Sex: Male

Ages: Under 12 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Males < 12 years of age
• Subjects with severe hemophilia A
• Previously treated with FVIII for > 50 exposure days

Exclusion criteria

• Subjects with current evidence of or history of inhibitors to FVIII
• Any other inherited or acquired bleeding disorder
• Platelet counts < 100,000/mm^3
• Creatinine > 2x the upper limit of normal
• Aspartate aminotransferase (AST) / Alanine aminotransferase (ALT) > 5x the upper limit of normal

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Single Group Assignment

Masking: None (Open label)

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73 participants in 3 patient groups

Main study

Experimental group

Description:

Participants were treated and prophylaxis administered with BAY94-9027 at a dose of 25-60 international units/kilogram (IU/kg) twice per week or 45-60 IU/kg every 5 days or 60 IU/kg every 7 days as an intravenous (IV) infusion as per clinical needs of each subject up to at least 50 exposure days (EDs) and a minimum of at least 6 months.

Treatment:

Biological: BAY94-9027

Biological: BAY94-9027

Biological: BAY94-9027

Part 2 (Expansion group)

Experimental group

Description:

Participants were administered with BAY94-9027 at a dose of 25-60 IU/kg twice per week for prophylaxis for 12 weeks.

Treatment:

Biological: BAY94-9027

Biological: BAY94-9027

Biological: BAY94-9027

Extension study

Experimental group

Description:

Participants were treated and prophylaxis administered with BAY94-9027 at a dose of 25- 60 IU/kg twice per week or 45-60 IU/kg every 5 days or 60 IU/kg every 7 days as an IV infusion as per clinical needs of each subject for at least 50 EDs or until marketing authorization of the drug.

Treatment:

Biological: BAY94-9027

Biological: BAY94-9027

Biological: BAY94-9027