Invasive Aspergillosis Clinical Trial
Official title:
A Multi-center, Open-label, Non-comparative Study to Evaluate the Efficacy and Safety of Micafungin Against Invasive Aspergillosis (CFDA Commitment)
The objective of this study is to evaluate the efficacy and safety of intravenous micafungin for the treatment of proven or probable fungal infections caused by Aspergillus sp. (Fungemia, respiratory mycosis, gastrointestinal mycosis) in adult patients in China.
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| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Recruiting |
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||
| Completed |
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Phase 3 | |
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Phase 1 | |
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Phase 2 | |
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N/A | |
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| Withdrawn |
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Phase 1 | |
| Withdrawn |
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Phase 1 | |
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Phase 1 | |
| Completed |
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Phase 1 | |
| Terminated |
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|
Phase 3 | |
| Active, not recruiting |
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N/A | |
| Terminated |
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Phase 3 | |
| Recruiting |
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Phase 3 | |
| Enrolling by invitation |
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| Not yet recruiting |
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Phase 3 | |
| Recruiting |
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| Terminated |
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N/A | |
| Recruiting |
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Surveillance for Nosocomial Infections in Pediatric Cancer Patients
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N/A | |
| Completed |
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|
Phase 4 |