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ClinicalTrials.gov record
Withdrawn Phase 4 Interventional

A Study to Evaluate the Effectiveness of Voriconazole + Micafungin Versus Voriconazole Alone for Invasive Aspergillosis

ClinicalTrials.gov ID: NCT00423163

Public ClinicalTrials.gov record NCT00423163. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 4:33 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Double-Blind, Randomized Controlled Trial of Voriconazole (VFEND®) Plus Micafungin (MYCAMINE™) Versus Voriconazole Plus Placebo in the Treatment of Patients With Proven or Probable Invasive Aspergillosis

Study identification

NCT ID
NCT00423163
Recruitment status
Withdrawn
Study type
Interventional
Phase
Phase 4
Lead sponsor
Astellas Pharma Inc
Industry
Enrollment
Not listed

Conditions and interventions

Interventions

  • micafungin Drug
  • voriconazole Drug

Drug

Eligibility (public fields only)

Age range
2 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 31, 2007
Primary completion
Not listed
Completion
Not listed
Last update posted
Sep 1, 2015

Started 2007

United States locations

U.S. sites
44
U.S. states
23
U.S. cities
44
Facility City State ZIP Site status
Not listed Birmingham Alabama
Not listed Fountain Valley California
Not listed Los Angeles California
Not listed Palo Alto California
Not listed Sacramento California
Not listed San Francisco California
Not listed Denver Colorado
Not listed Washington D.C. District of Columbia
Not listed Miami Florida
Not listed Atlanta Georgia
Not listed Chicago Illinois
Not listed Beech Grove Indiana
Not listed Indianapolis Indiana
Not listed Kansas City Kansas
Not listed Wichita Kansas
Not listed Lexington Kentucky
Not listed Baltimore Maryland
Not listed Bethesda Maryland
Not listed Boston Massachusetts
Not listed Charlestown Massachusetts
Not listed Worcester Massachusetts
Not listed Ann Arbor Michigan
Not listed Detroit Michigan
Not listed Grand Rapids Michigan
Not listed Minneapolis Minnesota
Not listed Rochester Minnesota
Not listed Omaha Nebraska
Not listed Albany New York
Not listed New York New York
Not listed Rochester New York
Not listed Winston-Salem North Carolina
Not listed Akron Ohio
Not listed Cincinnati Ohio
Not listed Columbus Ohio
Not listed Portland Oregon
Not listed Philadelphia Pennsylvania
Not listed Pittsburgh Pennsylvania
Not listed Dallas Texas
Not listed Houston Texas
Not listed San Antonio Texas
Not listed Charlottesville Virginia
Not listed Fairfax Virginia
Not listed Richmond Virginia
Not listed Madison Wisconsin

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00423163, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 1, 2015 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00423163 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →