Last updated on July 2019

Study Evaluating "Real World" Treatment Pattern in Previously Treated Hemophilia A Patients Receiving KOVALTRY (Octocog Alfa) for Routine Prophylaxis

Are you eligible to participate in this study?

You may be eligible for this study if you meet the following criteria:

  • Conditions: Hemophilia A
  • Age: - 100 Years
  • Gender: Male

Inclusion Criteria:

  • Male patients diagnosed with moderate to severe hemophilia A ( 5% FVIII:C (Factor VIII Coagulant activity))
  • Any age
  • 50 exposure days (EDs) to any FVIII product
  • Patients with or without history of inhibitors
  • Patient with previous history of inhibitors, with at least 2 consecutive negative inhibitor tests and on standard prophylaxis therapy for at least 1 year prior to study entry
  • No current evidence of FVIII inhibitor or clinical suspicion of FVIII inhibitor
  • Evidence of FVIII inhibitor as measured by the Nijmegen-modified Bethesda assay[<0.6 Bethesda units (BU/mL)] or Bethesda assay [< 1.0 BU/mL] in 2 on consecutives samples
  • Documented or clinical suspicion of shortened FVIII half-life (< 6 hrs)
  • Currently on or plan to start prophylaxis therapy with KOVALTRY
  • Written informed consent

Exclusion Criteria:

  • Patients participating in an investigational program with interventions outside of routine clinical practice
  • Patients with an additional diagnosis of any bleeding/coagulation disorder other than hemophilia A
  • Patients on Immune Tolerance Induction (ITI) treatment at the time of enrollment

Recruitment Status: Open

Brief Description Eligibility Contact Research Team

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