- Trials with a EudraCT protocol (205)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
205 result(s) found for: Fungal infections.
Displaying page 1 of 11.
EudraCT Number: 2008-007712-14 | Sponsor Protocol Number: 1120081 | Start Date*: 2009-01-17 | |||||||||||
Sponsor Name:Erasme Hospital | |||||||||||||
Full Title: Monitoring of serum concentrations of posaconazole given as prophylaxis or therapy. | |||||||||||||
Medical condition: fungal infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003717-33 | Sponsor Protocol Number: P02095 | Start Date*: 2005-09-13 | |||||||||||
Sponsor Name:SCHERING-PLOUGH | |||||||||||||
Full Title: Open-Label, limited access protocol of Posaconazole in invasive fungal infections. | |||||||||||||
Medical condition: Profilaxys of invasive mycotic infections in high risk neutropenic patients. | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002848-93 | Sponsor Protocol Number: UMCN-AKF13.02 | Start Date*: 2014-01-23 | |||||||||||
Sponsor Name:Radboud University Medical Centre | |||||||||||||
Full Title: Pharmacokinetics of micafungin (Mycamin ®) as antifungal prophylaxis given twice weekly intravenously compared to micafungin given daily to patients at risk for developing an invasive fungal disease. | |||||||||||||
Medical condition: prophylaxis for patients at high risk for invasive fungal diseases | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001182-87 | Sponsor Protocol Number: UMCN-AKF16.01 | Start Date*: 2017-01-10 | |||||||||||
Sponsor Name:Radboud University Medical Centre | |||||||||||||
Full Title: Pharmacokinetics of posaconazole (Noxafil(R)) as prophylaxis for invasive fungal disease | |||||||||||||
Medical condition: prophylaxis for patients at high risk for invasive fungal diseases | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-003745-40 | Sponsor Protocol Number: GS-IT-131-0151 | Start Date*: 2005-02-07 | |||||||||||
Sponsor Name:GILEAD SCIENCES S.R.L. | |||||||||||||
Full Title: Phase II pilot study on safety of administration of 3mg/kg/day three times a week until day 22 (21 days after transplantation day) and 7 mg/kg weekly from day 29 to the end of treatment ( day 50-8t... | |||||||||||||
Medical condition: Fungal Infection High risk patients undergoing allogeneic stem-cell transplantation. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000501-20 | Sponsor Protocol Number: A1501082 | Start Date*: 2017-03-09 | |||||||||||
Sponsor Name:Pfizer, Inc. | |||||||||||||
Full Title: Voriconazole In High-Risk Patients With Invasive Fungal Infections In Slovakia. An Open, Prospective, Non-comparative Study | |||||||||||||
Medical condition: Invasive Fungal Infections | |||||||||||||
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Population Age: In utero, Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-008382-35 | Sponsor Protocol Number: AIFA - FARM07YPBW | Start Date*: 2010-04-08 | |||||||||||
Sponsor Name:Azienda Ospedaliera di Perugia | |||||||||||||
Full Title: Open , multicenter, randomized trial comparing two therapeutic approaches for the treatment of invasive fungal infections in neutropenic onco-hematologic patients.Empiric vs. ``presumptive`` (pree... | |||||||||||||
Medical condition: opportunistic fungal infections in neutropenic onco-hematologic patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019562-91 | Sponsor Protocol Number: GS-EU-131-0247 | Start Date*: 2010-12-13 | |||||||||||
Sponsor Name:Gilead Sciences International Ltd | |||||||||||||
Full Title: A Phase 3, Double-Blind, Multicenter, Randomized, Placebo Controlled Study to Assess the Efficacy, Safety and Tolerability of Prophylactic Liposomal Amphotericin B (AmBisome®) for the Prevention of... | |||||||||||||
Medical condition: Invasive fungal infections (IFI) in subjects with Acute Lymphoblastic Leukemia (ALL) undergoing remission induction chemotherapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) PT (Completed) ES (Completed) DE (Completed) GR (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-006868-24 | Sponsor Protocol Number: UMCN-AKF-21.05 | Start Date*: 2022-08-02 | |||||||||||
Sponsor Name:Radboud university medical centre | |||||||||||||
Full Title: Pharmacokinetics of fluconazole given orally or intravenously as prophylaxis or therapy to children and adolescents with invasive fungal infections (FOCUS) | |||||||||||||
Medical condition: Invasive fungal disease | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002800-40 | Sponsor Protocol Number: A1501073 | Start Date*: 2006-02-09 | |||||||||||
Sponsor Name:Pfizer Ltd | |||||||||||||
Full Title: Prospective, Open-label, Comparative, Multicenter Study of Voriconazole Compared to Itraconazole for the Primary Prophylaxis of Invasive Fungal Infections (IFI) in Subjects with Allogeneic Hematopo... | |||||||||||||
Medical condition: Prophylaxis against invasive fungal infection following allogeneic hematopoietic stem cell transplantation. | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) CZ (Completed) ES (Completed) PT (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003306-33 | Sponsor Protocol Number: UMCN-AKF-14.04 | Start Date*: 2017-01-17 | |||||||||||
Sponsor Name:Radboud university medical center | |||||||||||||
Full Title: Liposomal amphotericin B (Ambisome) pharmacokinetics given as a single intravenous dose to obese patients (ASPEN). | |||||||||||||
Medical condition: Prophylaxis for patients at risk for invasive fungal infection due to gastric bypass surgery. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002271-97 | Sponsor Protocol Number: F901318C21 | Start Date*: 2017-04-07 | |||||||||||
Sponsor Name:F2G Limited | |||||||||||||
Full Title: An open label phase IIa clinical study to evaluate the safety and pharmacokinetics of oral F901318 (combined with fluconazole and posaconazole) for antifungal prophylaxis in patients undergoing che... | |||||||||||||
Medical condition: Invasive fungal disease in patients with acute myeloid leukemia under chemotherapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002613-35 | Sponsor Protocol Number: UMCN-AKF-18.07 | Start Date*: 2018-11-05 | |||||||||||
Sponsor Name:Radboud university medical centre | |||||||||||||
Full Title: Fluconazole pharmacokinetics, including bioavailability, in Obese subjects after an Intravenous and oral Administration (FOLIA). | |||||||||||||
Medical condition: Pharmacokinetics of fluconazole in obese subjects. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000919-33 | Sponsor Protocol Number: F901318C20 | Start Date*: 2016-10-12 | |||||||||||
Sponsor Name:F2G Limited | |||||||||||||
Full Title: An open label phase IIa clinical study to evaluate the safety and pharmacokinetics of intravenous and oral F901318 (combined with caspofungin) for antifungal prophylaxis in patients undergoing chem... | |||||||||||||
Medical condition: Infasive fungal disease in patients with acute myeloid leukemia under chemotherapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001633-41 | Sponsor Protocol Number: 18-01/Cic-C | Start Date*: 2019-06-18 | |||||||||||
Sponsor Name:Dermapharm AG | |||||||||||||
Full Title: Double-blind, randomised clinical study comparing efficacy and safety of Ciclopirox Olamine Cream 10 mg/g (Test) vs. Batrafen® Cream (Reference) vs. Vehicle in patients with skin mycoses | |||||||||||||
Medical condition: dermatomycoses | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000386-32 | Sponsor Protocol Number: F901318/0041 | Start Date*: 2022-01-21 | |||||||||||
Sponsor Name:F2G Ltd. | |||||||||||||
Full Title: A Phase III, adjudicator-blinded, randomised study to evaluate the efficacy and safety of treatment with olorofim versus treatment with AmBisome® followed by standard of care (SOC) in patients with... | |||||||||||||
Medical condition: invasive fungal infections due to Aspergillus spp. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) FR (Trial now transitioned) BE (Trial now transitioned) NL (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016936-11 | Sponsor Protocol Number: FAR01-2009 | Start Date*: 2011-05-12 | |||||||||||||||||||||||||||||||
Sponsor Name:Servicio de Farmacia. Hospital Universitario de Bellvitge. | |||||||||||||||||||||||||||||||||
Full Title: Estudio farmacocinético-farmacodinámico poblacional tras la administración oral o intravenosa de voriconazol en paciente crítico (fase IV) | |||||||||||||||||||||||||||||||||
Medical condition: paciente crítico en tratamiento con voriconazol oral o endovenoso | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002644-23 | Sponsor Protocol Number: MB_PDT_1 | Start Date*: 2020-07-23 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Dept. of Dermatology, Zealand University Hospital, Roskilde | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Photodynamic therapy of antifungal resistant dermatophytes | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Competent patients over 18 years old with mycological verified antifungal resistant dermatophytosis | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003172-39 | Sponsor Protocol Number: Mica1/2012 | Start Date*: 2013-05-23 |
Sponsor Name:Medizinische Universität Innsbruck, Abteilung für Hygiene und Medizinische Mikrobiologie | ||
Full Title: Micafungin-Deescaltion study: Evalutating the rate of breakthrough infections of micafungin followed by fluconazole versus fluconazole (or other azoles) in febrile patients | ||
Medical condition: All patients who are suspicious of suffering from invasive fungal infections are included. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-004981-85 | Sponsor Protocol Number: CD101.IV.3.08 | Start Date*: 2020-04-06 | |||||||||||
Sponsor Name:Cidara Therapeutics, Inc. | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-Blind Study of the Efficacy and Safety of Rezafungin for Injection Versus the Standard Antimicrobial Regimen to Prevent Invasive Fungal Diseases in Adults... | |||||||||||||
Medical condition: Invasive Fungal Diseases in Adults undergoing Allogeneic Blood and Marrow Transplantation (BMT) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) BE (Trial now transitioned) NL (Ongoing) GB (GB - no longer in EU/EEA) FR (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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