Trials / Terminated
TerminatedNCT00805740
An Evaluation Of The Effectiveness And Safety Of Anidulafungin Compared To Caspofungin For The Treatment Of Deep Tissue Infection Due To Candida
Efficacy And Safety Of Eraxis/Ecalta (Anidulafungin) Compared To Cancidas (Caspofungin) In Patients With Candida Deep Tissue Infection
- Status
- Terminated
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 41 (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 serious Candida infection. It is expected that anidulafungin will be at least as safe and as effective as the comparator drug, caspofungin.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Active anidulafungin | Subjects in this arm will receive active anidulafungin and placebo caspofungin |
| DRUG | Active Caspofungin | Subjects in this arm will receive active caspofungin and placebo anidulafungin |
Timeline
- Start date
- 2009-04-01
- Primary completion
- 2012-06-01
- Completion
- 2012-06-01
- First posted
- 2008-12-10
- Last updated
- 2013-08-01
- Results posted
- 2013-08-01
Locations
18 sites across 9 countries: United States, Belgium, Bulgaria, Canada, Netherlands, Portugal, Romania, Russia, Switzerland
Source: ClinicalTrials.gov record NCT00805740. Inclusion in this directory is not an endorsement.