Trials / Completed
CompletedNCT00168090
Study of Safety and Efficacy of Antihemophilic Factor/Von Willebrand Factor Complex in Surgical Subjects With Von Willebrand Disease (vWD)
Study of Safety and Efficacy of Antihemophilic Factor/Von Willebrand Factor Complex (Humate-P®) Using Individualized Dosing in Pediatric and Adult Surgical Subjects With Von Willebrand's Disease.
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 30 (planned)
- Sponsor
- CSL Behring · Industry
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to test the safety and effectiveness of Humate-P® to prevent bleeding in patients with von Willebrand Disease who are undergoing surgery.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Blood coagulation Factor VIII and vWF, human |
Timeline
- Start date
- 2001-10-01
- Completion
- 2006-05-01
- First posted
- 2005-09-14
- Last updated
- 2011-02-11
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00168090. Inclusion in this directory is not an endorsement.