Assessing Different FVIII Doses and Frequencies in Immune Tolerance Induction (ITI) with ADVATE Among Hemophilia a Boys with Inhibitor (INITIATE Study)
Recruiting
Phase 4
Interventional Study
Hemophilia a with Inhibitor
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
At a Glance
- Age
- 0 – 18
- Sex
- Male
- Trial phase
- Phase 4
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 110 (estimated)
- Sponsor
- Runhui WU · Other
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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 effecti…
Trial Locations
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Eligibility Criteria
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
Contacts