105
Participants
Start Date
June 30, 2007
Primary Completion Date
February 28, 2013
Study Completion Date
February 28, 2013
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"
Rho, Inc., Chapel Hill
BloodCenter of Wisconsin, Milwaukee
Skåne University Hospital, Malmo
Collaborators (1)
Versiti
OTHER
CSL Behring
INDUSTRY
Skane University Hospital
OTHER