Neutropenia Clinical Trial
Official title:
Phase I/II Study of the Safety, Tolerance and Pharmacokinetics of Anidulafungin in Immunocompromised Children With Fever and Neutropenia
Verified date | October 2008 |
Source | Pfizer |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Food and Drug Administration |
Study type | Interventional |
Anidulafungin is a medicine being developed for treatment of adults with certain kinds of fungal infections. This study is evaluating anidulafungin in children and adolescents who have fever and a low white blood cell count (neutropenia).
Status | Completed |
Enrollment | 25 |
Est. completion date | June 2004 |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 2 Years to 17 Years |
Eligibility |
- Children ages 2-17 years with fever and neutropenia. - The expected duration of neutropenia should be 10 days and due to cytotoxic chemotherapy or aplastic anemia. |
Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | Versicor | King of Prussia | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
Pfizer | Vicuron Pharmaceuticals |
United States,
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