Skip to main content
TrialFinder
TrialFinder is for informational purposes only and does not provide medical advice. Always talk to your doctor about whether a trial is right for you.
RECRUITINGPhase 4INTERVENTIONAL

Assessing Different FVIII Doses and Frequencies in Immune Tolerance Induction (ITI) with ADVATE Among Hemophilia a Boys with Inhibitor (INITIATE Study)

Assessing Different FVIII Dose and Frequency in Immune Tolerance Induction (ITI) with ADVATE Among Hemophilia a Boys with Inhibitor (INITIATE Study): a Multicenter Open-label Non-randomized Clinical Trial

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

Hemophilia A is a blood coagulation disorder caused by deficient or dysfunctional clotting factor VIII (FVIII) leading to incomplete haemostasis. Patients with severe Hemophilia A are predisposed to recurrent bleeding episodes (BEs) in joints and soft tissues that culminate in debiltating arthropathy and long-term morbidity. Prophylaxis with plasma-derived or recombinant FVIII concentrates effectively restores FVIII levels in patients with Hemophilia A, and significantly reduces the risk of bleeding. A critical concern for patients receiving FVIII replacement therapy is the development of neutralising antibodies (inhibitors) against the treatment. Inhibitors develop in up to 40% of patients with severe Hemophilia A when first exposed to FVIII treatment, typically within the first 20-30 exposure days (EDs) although a residual risk remains until after 75 EDs. Inhibitors preclude the use of FVIII replacement therapy for prevention and treatment of bleeding. Eradication of inhibitors therefore remains an important objective for Hemophilia A patients with inhibitors. Immune tolerance induction (ITI) therapy is the only clinically proven strategy for inhibitor eradication, and at least one attempt should be offered to patients with inhibitors. However, while ITI is well-studied and has a 60- 80% success rate, treatment regimens can be expensive and burdensome to patients. There are limited data on the use of different dose regimen of FVIII ITI in China. The INITIATE Study was designed to observe treatment strategies in patients with hemophilia A with inhibitors, with a focus on evaluating the safety and effectiveness of different dose regimens of ITI. The INITIATE Study includes multiple groups to explore factors that may affect ITI outcomes, and to explore the effects of different treatment methods on patient ITI biomarkers (genomics, transcriptomics, proteins (antibodies).

Who May Be Eligible (Plain English)

Who May Qualify: - Severe hemophilia A (FⅧ:C \<2%); - Positive for FVIII inhibitors; - No allergic reactions to FVIII concentrates. Who Should NOT Join This Trial: - Presence of other coagulation-related diseases, - Hematological disorders, - autoimmune conditions (where your immune system attacks your own body)s - malignancies Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * Severe hemophilia A (FⅧ:C \<2%); * Positive for FVIII inhibitors; * No allergic reactions to FVIII concentrates. Exclusion Criteria: * Presence of other coagulation-related diseases, * Hematological disorders, * autoimmune diseases * malignancies

Treatments Being Tested

DRUG

Advate®

Non-daily dose FVIII 50IU/kg.QoD or 100IU/kg.QoD

DRUG

Advate®

Daily dose FVIII 50IU/kg.QD or 100IU/kg.QD

DRUG

Advate®

Low dose FVIII 50IU/kg.QD or 100IU/kg.QoD

DRUG

Advate®

Medium and high dose FVIII ≥100IU/kg.QD

DRUG

Advate®

Medium and high dose FVIII ≥100IU/kg.QD with immunosuppressant agent(s)

Locations (1)

Beijing Children's hospitial
Beijing, Beijing Municipality, China