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Completed Phase 4 Interventional Results available

Study Will Evaluate The Safety And Efficacy Of Anidulafungin In Patients With Candidemia Or Invasive Candidiasis

ClinicalTrials.gov ID: NCT00496197

Public ClinicalTrials.gov record NCT00496197. 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 Oct 23, 2026, 5:35 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

Phase IV Open Label Non Comparative Trial Of IV Anidulafungin Followed By Oral Azole Therapy For The Treatment Of Candidemia And Invasive Candidiasis

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to further evaluate the safety and effectiveness of intravenous anidulafungin (Eraxis™) in patients with a diagnosis of candidemia or invasive candidiasis, which is a fungus infection of the blood or tissue. Currently the drug is approved for treatment using a daily dose of IV medication until 14 days after the fungus disappears from the blood. This study will evaluate the effectiveness of intravenous anidulafungin when it is administered for 5-28 days followed by oral antifungal medication. Study patients will be assessed for response to treatment throughout the study drug treatment period.

Study identification

NCT ID
NCT00496197
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Pfizer
Industry
Enrollment
282 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 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
Jul 2007 (Type not available)
Primary completion
Jun 2010 (Actual)
Completion
Jun 2010 (Actual)
Last update posted
Oct 3, 2011

2007 – 2010

United States locations

U.S. sites
39
U.S. states
19
U.S. cities
28
Facility City State ZIP Site status
Pfizer Investigational Site Birmingham Alabama 35233 —
Pfizer Investigational Site Birmingham Alabama 35294 —
Pfizer Investigational Site Little Rock Arkansas 72205 —
Pfizer Investigational Site Los Angeles California 90033 —
Pfizer Investigational Site San Francisco California 94115 —
Pfizer Investigational Site San Francisco California 94143 —
Pfizer Investigational Site Newark Delaware 19713 —
Pfizer Investigational Site Newark Delaware 19718 —
Pfizer Investigational Site Wilmington Delaware 19801 —
Pfizer Investigational Site Washington D.C. District of Columbia 20010 —
Pfizer Investigational Site Jacksonville Florida 32209 —
Pfizer Investigational Site Miami Florida 33136 —
Pfizer Investigational Site Orlando Florida 32801 —
Pfizer Investigational Site Orlando Florida 32806 —
Pfizer Investigational Site Orlando Florida 32819 —
Pfizer Investigational Site Atlanta Georgia 30322 —
Pfizer Investigational Site Springfield Illinois 62701 —
Pfizer Investigational Site Springfield Illinois 62702 —
Pfizer Investigational Site Springfield Illinois 62703-9248 —
Pfizer Investigational Site Springfield Illinois 62703 —
Pfizer Investigational Site Baltimore Maryland 21205 —
Pfizer Investigational Site Baltimore Maryland 21287 —
Pfizer Investigational Site Detroit Michigan 48201 —
Pfizer Investigational Site Detroit Michigan 48202 —
Pfizer Investigational Site Royal Oak Michigan 48073 —
Pfizer Investigational Site Minneota Minnesota 55455 —
Pfizer Investigational Site Butte Montana 59701 —
Pfizer Investigational Site Camden New Jersey 08103 —
Pfizer Investigational Site Albany New York 12208 —
Pfizer Investigational Site Buffalo New York 14263 —
Pfizer Investigational Site Rochester New York 14642 —
Pfizer Investigational Site Greenville North Carolina 27834-6028 —
Pfizer Investigational Site Greenville North Carolina 27834 —
Pfizer Investigational Site Portland Oregon 97239 —
Pfizer Investigational Site Philadelphia Pennsylvania 19140 —
Pfizer Investigational Site Pittsburgh Pennsylvania 15213 —
Pfizer Investigational Site West Reading Pennsylvania 19611 —
Pfizer Investigational Site Charleston South Carolina 29414 —
Pfizer Investigational Site Houston Texas 77030 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00496197, 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 Oct 3, 2011 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00496197 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →