Non-Interventional Post Marketing Surveillance Study To Observe The Safety And Efficacy Of Vfend® IV
NCT01073618 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 692
Last updated 2012-06-07
Summary
This is non-interventional study of voriconazole IV formulation in clinical use, which was mandated by the Korean government agency following the approval of Vfend in the Republic of Korea.
Conditions
- Serious Fungal Infections
Interventions
- DRUG
-
voriconazole IV
6 mg/kg iv q 12 hours (loading) then maintenance
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Pfizer CT.gov Call Center · Pfizer
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2006-03-31
- Primary Completion
- 2009-10-31
- Completion
- 2009-10-31
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