CompletedNCT00701545
A Canadian Study to Assess the Safety of Humate-P® Ivr (Infusion Volume Reduced)
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
- David G. Barnes, Dr.CSL Behring Canada
- Enrollment
- 21 target
- Eligibility
- All sexes
- Timeline
- 2008 – 2009
Study locations (1)
- Toronto, Canada
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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