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

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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

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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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01073618 on ClinicalTrials.gov