- Trials with a EudraCT protocol (101)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
101 result(s) found for: Mycoses AND Fungal Diseases.
Displaying page 2 of 6.
EudraCT Number: 2007-004645-15 | Sponsor Protocol Number: P03579 | Start Date*: 2008-03-14 | ||||||||||||||||
Sponsor Name:Schering Plough Research Institute | ||||||||||||||||||
Full Title: Phase 1B Study of the Safety, Tolerance, and Pharmacokinetics of Oral Posaconazole in Immunocompromised Children With Neutropenia | ||||||||||||||||||
Medical condition: treatment and prophylaxis of invasive fungal infections; oropharyngeal candidiasis (OPC) and refractory OPC | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) DE (Prematurely Ended) NL (Prematurely Ended) GR (Prematurely Ended) Outside EU/EEA | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-002807-10 | Sponsor Protocol Number: 5592-097 | Start Date*: 2015-09-02 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Study of the Safety, Tolerability, and Pharmacokinetics of Intravenous (IV) and Powder for Oral Suspension Formulations of Posaconazole (POS) in Immunocompromised Pediatric Subjects with Neutropenia | |||||||||||||
Medical condition: Prophylaxis of invasive fungal infections in immunocompromised pediatric subjects with neutropenia or expected neutropenia. | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) NO (Completed) SE (Completed) DK (Completed) CZ (Completed) ES (Completed) BE (Completed) IT (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003087-20 | Sponsor Protocol Number: 800_OPBG_2014 | Start Date*: 2014-11-12 | |||||||||||||||||||||
Sponsor Name:IRCCS Ospedale Pediatrico Bambino Gesù | |||||||||||||||||||||||
Full Title: Determination of Plasmatic and CSF Levels Of High Doses Of Micafungin in Neonates Suffering from Systemic Candidiasis and/or Candida meningitis. | |||||||||||||||||||||||
Medical condition: Systemic Candidiasis and/or Candida Meningitis | |||||||||||||||||||||||
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Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
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: 2014-004183-38 | Sponsor Protocol Number: A1501007 | Start Date*: 2015-05-21 | |||||||||||
Sponsor Name:Pfizer, Inc. | |||||||||||||
Full Title: An open, intravenous multiple dose, multi-centre study to investigate the pharmacokinetics, safety and toleration of Voriconazole in children aged 2-12 years who require treatment for the preventio... | |||||||||||||
Medical condition: Systemic Fungal Infection | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003722-24 | Sponsor Protocol Number: MOB015B-II | Start Date*: 2012-10-17 |
Sponsor Name:Moberg Derma AB | ||
Full Title: An open, single-centre pilot study of efficacy and safety of topical MOB015B in the treatment of distal subungual onychomycosis (DSO) | ||
Medical condition: Distal subungual onychomycosis (DSO) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-003463-22 | Sponsor Protocol Number: CLOTOT3-16IA03 | Start Date*: 2020-04-29 | |||||||||||
Sponsor Name:Laboratorios Salvat, S.A. | |||||||||||||
Full Title: A Phase III, Multicenter, Randomized, Double-Blind Clinical Trial to Assess the Efficacy and Safety of Clotrimazole 1% Otic Solution Compared to Placebo for the Treatment of Fungal Otitis Externa (... | |||||||||||||
Medical condition: Fungal Otitis Externa (Otomycosis) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) PT (Completed) BG (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004184-21 | Sponsor Protocol Number: A1501037 | Start Date*: 2015-05-21 | |||||||||||
Sponsor Name:Pfizer, Inc. | |||||||||||||
Full Title: An open-label, intravenous to oral switch, multiple dose, multi-centre study to investigate the pharmacokinetics, safety and tolerability of Voriconazole in hospitalized children aged 2 to <12 year... | |||||||||||||
Medical condition: Systemic fungal infection | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000559-42 | Sponsor Protocol Number: S54931 | Start Date*: 2013-03-01 | |||||||||||
Sponsor Name:University Hospitals Leuven | |||||||||||||
Full Title: Plasma protein binding characteristics of voriconazole in specific subsets of patients | |||||||||||||
Medical condition: Patients suffering from an invasive fungal infection, treated with intravenous or oral voriconazole. | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002085-12 | Sponsor Protocol Number: S54252 | Start Date*: 2012-06-11 | |||||||||||
Sponsor Name:University Hospitals Leuven | |||||||||||||
Full Title: Pharmacokinetic evaluation of the voriconazole IV to oral switch | |||||||||||||
Medical condition: Adult and pediatric hematology patients treated with intravenous voriconazole to cure an invasive fungal infection, and ready to switch from intravenous to oral administration of voriconazole | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001396-37 | Sponsor Protocol Number: S52913 | Start Date*: 2012-03-29 | |||||||||||
Sponsor Name:University Hospitals Leuven, Belgium | |||||||||||||
Full Title: Determination of voriconazole in saliva - Validation in specifif subsets of patients. | |||||||||||||
Medical condition: patients suffering from an invasive fungal infection, treated with intravenous or oral voriconazole. | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005214-49 | Sponsor Protocol Number: 9463-EC-0001 | Start Date*: 2009-10-30 | |||||||||||
Sponsor Name:Astellas Pharma Europe Ltd | |||||||||||||
Full Title: Randomized, Open label, Non-inferiority Study of Micafungin versus Standard Care for the Prevention of Invasive Fungal Disease in High Risk Liver Transplant Recipients | |||||||||||||
Medical condition: Fungal infection. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) IE (Completed) HU (Completed) ES (Completed) FR (Completed) DE (Completed) PT (Completed) CZ (Completed) IT (Completed) SE (Completed) AT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003140-68 | Sponsor Protocol Number: MK5592-105-00 | Start Date*: 2012-10-29 | |||||||||||
Sponsor Name:MSD | |||||||||||||
Full Title: A Pharmacokinetic Analysis of Posaconazole in the Plasma and Alveolar Compartment of Lung Transplant Recipients | |||||||||||||
Medical condition: Invasive fungal infection (IFI) in lung transplant patients with and without cystic fibrosis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000780-24 | Sponsor Protocol Number: 9463-CL-2303 | Start Date*: 2012-07-24 |
Sponsor Name:Astellas Pharma Global Development, Inc. | ||
Full Title: A Phase 3, Randomized, Double-Blind, Multi-Center Study to Compare the Efficacy and Safety of Micafungin Versus Amphotericin B Deoxycholate for the Treatment of Neonatal Candidiasis | ||
Medical condition: Neonatal Candidiasis | ||
Disease: | ||
Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: GR (Completed) HU (Completed) BG (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-000381-29 | Sponsor Protocol Number: SCY-078-301 | Start Date*: 2017-07-17 |
Sponsor Name:SCYNEXIS, Inc. | ||
Full Title: Open-Label Study to Evaluate the Efficacy and Safety of Ibrexafungerp in Patients with Fungal Diseases that are Refractory to, Resistant to or Intolerant of Standard Antifungal Treatment (FURI) | ||
Medical condition: Patients > 18 years of age with a documented invasive and/or severe fungal disease that has been intolerant, resistant or refractory (rIFI) to Standard of Care (SoC) antifungal treatment. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) AT (Completed) ES (Ongoing) GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2018-000240-26 | Sponsor Protocol Number: PC_ASP_002 | Start Date*: 2019-05-17 | |||||||||||
Sponsor Name:Pulmocide Ltd | |||||||||||||
Full Title: An open-label, pilot study to assess safety, tolerability, pharmacokinetics and effects of inhaled PC945 in the pre-emptive treatment of Aspergillus fumigatus colonisation in lung transplant recipi... | |||||||||||||
Medical condition: Pre-emptive treatment of Aspergillus fumigatus colonisation in lung transplant recipients | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001133-14 | Sponsor Protocol Number: A1501088 | Start Date*: 2012-03-06 |
Sponsor Name:Pfizer Inc. 235 East 42nd Street, New York, NY 10017 | ||
Full Title: An Open Label, Intravenous to Oral Switch, Multiple Dose Study to Evaluate the Pharmacokinetics, Safety and Tolerability of Voriconazole in Immunocompromised Children Aged 2 to <12 Years who are at... | ||
Medical condition: Invasive fungal infections | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2012-001151-39 | Sponsor Protocol Number: A1501081 | Start Date*: 2012-03-06 |
Sponsor Name:Pfizer Inc. 235 East 42nd Street, New York, NY 10017 | ||
Full Title: An Open Label, Intravenous to Oral Switch, Multiple Dose Study to Evaluate the Pharmacokinetics, Safety and Tolerability of Voriconazole in Immunocompromised Adolescents Aged 12 to <17 Years who ar... | ||
Medical condition: Invasive fungal infections | ||
Disease: | ||
Population Age: Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2012-000904-14 | Sponsor Protocol Number: MICA_HDF | Start Date*: 2012-07-19 | |||||||||||
Sponsor Name:Medizinische Universität Wien | |||||||||||||
Full Title: PHARMACOKINETICS OF MICAFUNGIN DURING CONTINUOUS VENOVENOUS HEMOFILTRATION | |||||||||||||
Medical condition: Suspected or proven candida infection requiring parenteral antifungal therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000244-26 | Sponsor Protocol Number: PC-ASP-004 | Start Date*: 2018-08-21 | ||||||||||||||||
Sponsor Name:Pulmocide Ltd | ||||||||||||||||||
Full Title: A double-blind, placebo-controlled study to assess the effects of inhaled PC945 in the treatment of culture-positive Aspergillus or Candida fungal bronchitis in subjects with moderate to severe ast... | ||||||||||||||||||
Medical condition: Pulmonary aspergillosis and candidiasis of lung | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
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