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
| 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
- 2009-08-01
- 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.