RecruitingPhase 4NCT02472665

Efficacy and Safety of Fanhdi®, a High-purity Von Willebrand Containing FVIII Concentrate, in Pediatric Patients With Von Willebrand Disease

Evaluation of the Pharmacokinetic Profile, Clinical Efficacy and Safety of the Von Willebrand Factor Contained in FANHDI® (Double-inactivated Human Anti-hemophilic Factor) in Pediatric Subjects With Severe Von Willebrand Disease


Sponsor

Grifols Therapeutics LLC

Enrollment

8 participants

Start Date

Dec 1, 2013

Study Type

INTERVENTIONAL

Conditions

Summary

Multicenter, prospective, non-controlled study in a pediatric cohort (\<6 years-old) with severe (type 2 or 3) hereditary Von Willebrand Disease (VWD).


Eligibility

Min Age: 2 MonthsMax Age: 6 Years

Inclusion Criteria3

  • Subjects diagnosed with severe (type 2 or 3) hereditary VWD (VWF:RCo<15-20 IU/dL), or VWF:Act<15-20 IU/dL.
  • Subjects under 6 years of age.
  • Signed informed consent form (ICF) provided by an authorized representative on behalf of the subject in accordance with local law and institutional policy.

Exclusion Criteria13

  • Subjects diagnosed with acquired VWD.
  • Subjects with active bleeding at the time of the first infusion or within 10 days prior to the infusion.
  • Subjects who have been treated with DDAVP or another FVIII containing VWF concentrate during the 5 days prior to the infusion of the Fanhdi. This treatment-free period may be reduced to 3 days for subjects with type 3 VWD.
  • Subject who are positive for anti-VWF or anti-FVIII antibodies (≥0.5 Bethesda Units) or has been positive in the history of their disease.
  • Subjects with a known allergies/intolerance to any substance contained in Fanhdi.
  • Subjects with a known history of anaphylactic reaction(s) to blood or blood components.
  • Subjects presenting severe platelet activity dysfunction due to the use of drugs (aspirin, other nonsteroidal anti-inflammatory drugs \[NSAIDs\], etc.) or a congenital or acquired platelet function disorder or other concomitant processes that may interfere with coagulation.
  • Subjects have a known previous infection with hepatitis A virus (HAV), hepatitis B virus (HBV), hepatitis C virus (HCV), or human immunodeficiency virus (HIV), or have clinical signs and symptoms consistent with current HAV, HBV, HCV or HIV infection.
  • Subjects presenting anemia (hemoglobin <11 g/dL).
  • Subjects diagnosed with metabolic diseases that are not clinically controlled, such as diabetes mellitus, which could potentially interfere with the interpretations of the study.
  • Participated in another clinical trial within 30 days prior to the screening visit or has received any investigational product (IP) within 3 months prior to the screening visit.
  • If it is anticipated that the subject will be treated with other products containing FVIII or VWF different from Fanhdi throughout the subject's participation.
  • Subjects who, in the opinion of the investigator, may have compliance problems with the protocol.

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Interventions

DRUGplasma-derived FVIII/VWF concentrate

1 single dose of 80 IU/kg VWF:RCo of Fanhdi will be administered


Locations(4)

Hospital Sant Joan de Déu Barcelona

Esplugues de Llobregat, Barcelona, Spain

Hospital Universitario La Paz

Madrid, Spain

Hospital Universitario Virgen del Rocío

Seville, Spain

Hospital Universitario Miguel Servet

Zaragoza, Spain

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NCT02472665


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