VL-2397 Compared to Standard First-Line Treatment for Invasive Aspergillosis (IA) in Adults
Stopped early · Phase 2
Conditions studied: Invasive Aspergillosis, Invasive Pulmonary Aspergillosis
In brief
The purpose of the trial is to evaluate the safety and efficacy of a new antifungal with a novel mechanism of action in immunocompromised adults with invasive aspergillosis.
Key facts
- Study ID
- NCT03327727
- Run by
- Vical
- People needed
- 4
- Starts
- 2018-02-20
- Expected to finish
- 2019-01-14
- Last updated by the study team
- 2019-02-27
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Acute Leukemia (AML or ALL) patient or allo-HCT recipient with a diagnosis of IA
You may not qualify if…
- Pregnant or breastfeeding
- IA involving sites other than lungs and sinuses
- Graft failure, acute or extensive chronic GvHD
- Uncontrolled diabetes
Where it is running
- University of Alabama at Birmingham Hospital, Division of Infectious Diseases — Birmingham, Alabama, United States
- UC San Diego Moores Cancer Center — La Jolla, California, United States
- UC Davis Health, Dept. of Internal Medicine, Div. of Infectious Diseases — Sacramento, California, United States
- Christiana Care Health Services, Department of Medicine — Newark, Delaware, United States
- Medical College of Georgia at Augusta University — Augusta, Georgia, United States
- DMC Harper University Hospital — Detroit, Michigan, United States
- University of Minnesota, Department of Medicine — Minneapolis, Minnesota, United States
- Washington University School of Medicine, Division of Infectious Disease — St Louis, Missouri, United States
- The University of Texas Health Science Center, Department of Internal Medicine — Houston, Texas, United States
- Fred Hutchinson Cancer Research Center (FHCRC) — Seattle, Washington, United States
- Medical College of Wisconsin — Milwaukee, Wisconsin, United States
- University Hospital Antwerp (UZA), Department of Hematology — Edegem, Antwerp, Belgium
- General Hospital Saint-Jan, Department of Hematology — Bruges, Belgium
- Jules Bordet Institute, Department of Infectious Disease — Brussels, Belgium
- University Hospitals Leuven, Campus Gasthuisberg, Department of Hematology — Leuven, Belgium
- UCL Mont-Godinne University Hospitals, Department of Hematology — Yvoir, Belgium
- Hamilton Health Sciences, Infectious Disease Research — Hamilton, Ontario, Canada
- Toronto General Hospital — Toronto, Ontario, Canada
- McGill University Health Centre (MUHC), Division of Infectios Diseases — Montreal, Quebec, Canada
- Grenoble University Hospital Center, Department of Hematology — Grenoble, France
- South Lyon Hospital Center — Pierre-Bénite, France
- Hautepierre Hospital — Strasbourg, France
- University Hospital Jena — Jena, Germany
- Hospital Neuperlach - Municipal Hospital Munich GmbH, Clinic of Hematology and Oncology — Munich, Germany
- Chonnam National University — Hwasun, South Korea
Full record on ClinicalTrials.gov
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