The purpose of this study is to evaluate the safety and effectiveness of micafungin in combination with AmBisome as first-line therapy in the treatment of invasive aspergillosis.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
2
IV
IV
Unnamed facility
Washington D.C., District of Columbia, United States
Unnamed facility
Atlanta, Georgia, United States
Unnamed facility
Ann Arbor, Michigan, United States
Unnamed facility
Detroit, Michigan, United States
Incidence of treatment response defined as complete or partial response
Time frame: Day 28, end of combined therapy and Day 84
Clinical Response
Time frame: Day 28, end of combined therapy and Day 84
Radiological Response
Time frame: Day 28, end of combined therapy and Day 84
Mycological Response
Time frame: Day 28, end of combined therapy and Day 84
Survival at Day 84
Time frame: Day 84
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Unnamed facility
St Louis, Missouri, United States
Unnamed facility
Memphis, Tennessee, United States
Unnamed facility
Houston, Texas, United States