The Von Willebrand Disease (VWD) International Prophylaxis Study

CompletedOBSERVATIONAL
Enrollment

105

Participants

Timeline

Start Date

June 30, 2007

Primary Completion Date

February 28, 2013

Study Completion Date

February 28, 2013

Conditions
Von Willebrand Disease
Interventions
DRUG

VWF/FVIII products

"Participants in the prospective phase of the study undergo an escalation of treatment from receipt of one to three levels of VWD product. All subjects enrolled will begin treatment on the level one and remain on this regimen for the duration of follow-up, or until they meet the criteria for escalation to level two or three (if indeed they do meet the criteria.)~Dosing for joint bleeding, epistaxis, and GI bleeding indications: 50 U RCo/kg once per week, 50 U RCo/kg twice per week, or 50 U RCo/kg three times per week.~Dosing for menorrhagia: 50 U RCo/kg on day 1 of menses for 2 cycles, 50 U RCo/kg on days 1 and 2 of menses for 2 cycles, or 50 U RCo/kg on days 1, 2, and 3 of menses"

Trial Locations (3)

27517

Rho, Inc., Chapel Hill

53201-2178

BloodCenter of Wisconsin, Milwaukee

SE-20502

Skåne University Hospital, Malmo

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Versiti

OTHER

collaborator

CSL Behring

INDUSTRY

lead

Skane University Hospital

OTHER

NCT00557908 - The Von Willebrand Disease (VWD) International Prophylaxis Study | Biotech Hunter | Biotech Hunter