Clinical Trials Directory

Trials / Terminated

TerminatedNCT00806351

An Evaluation Of The Effectiveness And Safety Of Anidulafungin Compared To Caspofungin For The Treatment Of Serious Fungal Infection Due To Candida In Patients With A Dysfunctional Immune System

Efficacy And Safety Of Eraxis/Ecalta (Anidulafungin) Compared To Cancidas (Caspofungin) In Neutropenic Patients With Invasive Candida Infection

Status
Terminated
Phase
Phase 3
Study type
Interventional
Enrollment
21 (actual)
Sponsor
Pfizer · Industry
Sex
All
Age
16 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to gather information on the use of anidulafungin for the treatment of Candida infection in patients with an abnormal immune system. It is expected that anidulafungin will be at least as safe and as effective as the comparator drug, caspofungin.

Conditions

Interventions

TypeNameDescription
DRUGActive AnidulafunginSubjects in this arm will receive active anidulafungin and placebo caspofungin
DRUGActive CaspofunginSubjects in this arm will receive active caspofungin and placebo anidulafungin

Timeline

Start date
2009-08-01
Primary completion
2011-10-01
Completion
2011-10-01
First posted
2008-12-10
Last updated
2012-12-20
Results posted
2012-12-20

Locations

10 sites across 6 countries: Bosnia and Herzegovina, France, Italy, Poland, Russia, Slovakia

Source: ClinicalTrials.gov record NCT00806351. Inclusion in this directory is not an endorsement.