CompletedPHASE2, PHASE3NCT00941616
Study of a pd VWF/FVIII Concentrate, Biostate®, in Subjects With Von Willebrand Disease
Studying Von Willebrand disease
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- CSL Behring
- Principal Investigator
- Program Director, Clinical R&DCSL Behring
- Intervention
- Biostate®(biological)
- Enrollment
- 22 target
- Eligibility
- 12 years · All sexes
- Timeline
- 2009 – 2012
Study locations (5)
- Study Site, Sofia, Bulgaria
- Study Site, Warsaw, Poland
- Study Site, Wroclaw, Poland
- Study Site, Barnaul, Russia
- Study Site, Lviv, Ukraine
Collaborators
Parexel
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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