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Sponsor: Pfizer
Conditions: Invasive Aspergillosis, Mucormycosis
Interventions: Isavuconazole
Countries: France, Germany, Italy, Spain, United Kingdom
This is a non-interventional medical chart review study aiming to examine the effectiveness, safety, and treatment patterns of isavuconazole in 5 European countries (France, Germany, Italy, Spain, and United Kingdom). Eligible patients are adults who have been treated with isavuconazole in routine practice at participating sites since 15 October, 2015 or since the date of launch in the country if it is after 15 October, 2015 until 30 June, 2019. As this is an observational study, patients will be treated based on the standard of care at the discretion of their physician. No drugs will be supplied for this study and patients will receive treatment through standard local practice.
Sex: ALL
Age: 18 Years to —
Healthy volunteers: No
Study type: OBSERVATIONAL
Inclusion Criteria: 1. Hospitalized patient must be aged ≥ 18 years at the time of isavuconazole initiation 2. Patient must have a record of a diagnosis of invasive aspergillosis or mucormycosis in their medical record at the time isavuconazole was initiated (regardless of whether this diagnosis is suspected or confirmed ) 3. Patient must have received at least one dose of isavuconazole during the eligibility period (October 15, 2015, to June 30, 2019) Exclusion Criteria: 1\. Patients who did not receive at least one dose of isavuconazole for treatment of invasive aspergillosis or mucormycosis within the eligibility period
- Limoges, France
- Paris, France
- Strasbourg, France
- Cologne, Germany
- Frankfurt, Germany
- Munich, Germany
- Ulm, Germany
- Turin, Piedmont, Italy
- Barcelona, Spain
- Barcelona, Spain
- Madrid, Spain
- Santander, Spain
- Zaragoza, Spain
- Cambridge, United Kingdom
- London, United Kingdom