- Trials with a EudraCT protocol (55)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
55 result(s) found for: Fungi.
Displaying page 1 of 3.
EudraCT Number: 2006-005003-33 | Sponsor Protocol Number: WSA-CS-003 | Start Date*: 2008-06-26 | |||||||||||
Sponsor Name:Astellas Global Pharma Development, Inc | |||||||||||||
Full Title: Open label study of isavuconazole in the treatment of patients with aspergillosis and renal impairment or of patients with invasive fungal disease caused by rare moulds, yeasts or dimorphic fungi. | |||||||||||||
Medical condition: Invasive fungal disease caused by Aspergillus species in patients with renal impairment as well as disease caused by rare moulds, yeasts or dimorphic fungi. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) BE (Completed) HU (Completed) CZ (Prematurely Ended) DE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003868-59 | Sponsor Protocol Number: WSA-CS-004 | Start Date*: 2011-05-12 | |||||||||||
Sponsor Name:Astellas Global Pharma Development, Inc. | |||||||||||||
Full Title: A phase III, double blind, randomized study to evaluate safety and efficacy of BAL8557 versus voriconazole for primary treatment of invasive fungal disease caused by Apsergillus species or other fi... | |||||||||||||
Medical condition: Invasive fungal disease caused by Aspergillus species or other filamentous fungi. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) HU (Completed) ES (Completed) NL (Completed) IT (Completed) GB (Completed) CZ (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005707-92 | Sponsor Protocol Number: 16-03/MicoFlu-C | Start Date*: 2016-11-07 | |||||||||||
Sponsor Name:Dermapharm AG | |||||||||||||
Full Title: Double-blind, randomised clinical study comparing efficacy and safety of Miconazole 2% Fluprednidene 0.1% Cream (Test) vs. Vobaderm® Cream (Reference) vs. Vehicle in patients with moderate to sever... | |||||||||||||
Medical condition: moderate to severely inflamed candidiasis of the skin | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001386-33 | Sponsor Protocol Number: APX001-202 | Start Date*: 2019-08-20 | |||||||||||
Sponsor Name:Amplyx Pharmaceuticals, Inc., a wholly owned subsidiary of Pfizer, Inc. | |||||||||||||
Full Title: A Phase 2, Open-Label Study to Evaluate the Safety and Efficacy of APX001 in the Treatment of Patients with Invasive Mold Infections Caused by Aspergillus Species or Rare Molds | |||||||||||||
Medical condition: Treatment of patients with invasive mold infections (IMIs) caused by Aspergillus species (spp.) or rare molds | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001010-42 | Sponsor Protocol Number: 19-01/MicoFlu-C | Start Date*: 2019-10-16 | |||||||||||
Sponsor Name:Dermapharm AG | |||||||||||||
Full Title: Double-blind, randomised clinical study comparing efficacy and safety of Miconazole 2%_Fluprednidene 0.1% Cream (Test) vs. Vobaderm® Cream (Reference) vs. Vehicle in patients with moderate to sever... | |||||||||||||
Medical condition: moderate to severely inflamed candidiasis of the skin | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003790-65 | Sponsor Protocol Number: 21-01/ClotriBet-S | Start Date*: 2022-02-11 | |||||||||||
Sponsor Name:Dermapharm AG | |||||||||||||
Full Title: Double-blind, randomised clinical study comparing efficacy and safety of Mecloderm® Ointment (Test) vs. Lotricomb® Ointment (Reference) vs. Vehicle in patients with moderate to severely inflamed ca... | |||||||||||||
Medical condition: moderate to severely inflamed candidiasis of the skin | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001290-17 | Sponsor Protocol Number: F901318/0032 | Start Date*: 2018-03-30 |
Sponsor Name:F2G Biotech GmbH (FN 483749 x) | ||
Full Title: An open-label single-arm Phase IIb study of F901318 as treatment of invasive fungal infections due to Lomentospora prolificans, Scedosporium spp., Aspergillus spp., and other resistant fungi in pat... | ||
Medical condition: invasive fungal infections due to Lomentospora prolificans, Scedosporium spp., Aspergillus spp., and other resistant fungi | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) ES (Ongoing) NL (Completed) DE (Completed) GB (GB - no longer in EU/EEA) PL (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-003416-31 | Sponsor Protocol Number: FAEDV-2012-01 | Start Date*: 2013-02-22 |
Sponsor Name:Fundación Academia Española de Dermatología y Venereología | ||
Full Title: Multicenter, randomized, open clinical trial comparing three sessions of methyl-aminolevulinate 16% (Metvix®) photodynamic therapy versus a group without photodynamic therapy to treat onychomycosis. | ||
Medical condition: onychomycosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-000801-39 | Sponsor Protocol Number: PsAer-IgY | Start Date*: 2011-08-31 | |||||||||||
Sponsor Name:Mukoviszidose Institute gGmbH | |||||||||||||
Full Title: Prospective randomized, placebo-controlled, double blind, multicenter study (phase III) to evaluate clinical efficacy and safety of avian polyclonal anti-Pseudomonas antibodies (IgY) in prevention ... | |||||||||||||
Medical condition: Cystic fibrosis (CF) is a chronic and progressive genetic disease of the body's exocrine glands. CF especially affects the respiratory system. A common effect leads to massive production of abnorma... | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) SE (Completed) BE (Completed) IT (Completed) IE (Completed) HU (Completed) AT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000561-31 | Sponsor Protocol Number: PM1331 | Start Date*: 2015-06-15 | |||||||||||
Sponsor Name:Polichem S.A. | |||||||||||||
Full Title: A MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PARALLEL, VEHICLE-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF P-3058 10% NAIL SOLUTION IN THE TREATMENT OF ONYCHOMYCOSIS | |||||||||||||
Medical condition: Mild to moderate distal subungual Onychomycosis caused by Dermatophytes | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) LV (Completed) BG (Completed) SE (Completed) DE (Completed) SK (Completed) BE (Completed) PL (Completed) CZ (Completed) LT (Completed) GR (Completed) IS (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002579-16 | Sponsor Protocol Number: CF001 | Start Date*: 2018-08-26 | |||||||||||
Sponsor Name:Karolinska University Hospital, Stockholm CF center | |||||||||||||
Full Title: Evaluation of the possible use of analysis of posaconazole in exhaled breath as a surrogate marker for the lung to monitor adequate dosages of posaconazole in CF patients treated for Aspergillus sp... | |||||||||||||
Medical condition: Cystic Fibrosis (CF) is the most common life–limiting autosomal recessive disease among people of European heritage. The condition is a result of a mutation in the cystic fibrosis transmembrane con... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 2017-003665-10 | Sponsor Protocol Number: RBH2017/001 | Start Date*: 2020-02-25 | |||||||||||
Sponsor Name:Royal Brompton and Harefield NHS Foundation Trust | |||||||||||||
Full Title: A single-centre study of the relationship between eosinophil activation and the lung microbiome in severe eosinophilic asthma (SEA) and the effect of benralizumab on these factors | |||||||||||||
Medical condition: Severe Eosinophilic Asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002408-42 | Sponsor Protocol Number: ASPER-III-19-1 | Start Date*: 2020-02-07 | |||||||||||
Sponsor Name:LABORATOIRES SMB S.A. | |||||||||||||
Full Title: A Phase 3, Double Blind, Multicentric, Randomised, Placebo-Controlled Study to Assess the Efficacy, Safety and Tolerability of Itraconazole Dry Powder for Inhalation for the Prevention of Invasive ... | |||||||||||||
Medical condition: prevention of invasive mould disease | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) BG (Prematurely Ended) ES (Prematurely Ended) PL (Prematurely Ended) BE (Completed) IT (Prematurely Ended) RO (Ongoing) | |||||||||||||
Trial results: View results |
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: 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: 2011-003087-70 | Sponsor Protocol Number: PM1125 | Start Date*: 2011-12-02 |
Sponsor Name:Polichem SA | ||
Full Title: Randomized, open-label, controlled study on the efficacy of Ciclopoli® (ciclopirox 8% nail lacquer) versus Loceryl® (amorolfine 5% nail lacquer) on the culture conversion to negative in patients w... | ||
Medical condition: distal subungual onychomycosis without lunula involvement due to fungal nail pathogens (dermatophytes, white yeasts and/or Scopulariopsis spp. and/or Fusarium spp.) affecting at least one big toenail | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: LV (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-000376-41 | Sponsor Protocol Number: VORIGENIPHARM | Start Date*: 2019-06-18 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Fundación de Investigación del Hospital Universitario La Paz (FIBHULP) | |||||||||||||||||||||||||||||||||||||||||||
Full Title: Randomized and multicenter clinical trial to evaluate the effectiveness and efficiency of a voriconazole preemptive genotyping strategy in patients with risk of aspergillosis. | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: Invasive fungal disease in the hematologic patient. | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004356-20 | Sponsor Protocol Number: DCS-002 | Start Date*: 2011-10-31 |
Sponsor Name:Pergamum AB | ||
Full Title: A randomised, parallel-group, double-blind, placebo-controlled study of DPK-060 to investigate clinical safety and efficacy in patients with acute external otitis | ||
Medical condition: Acute external otitis (EO) | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-003784-19 | Sponsor Protocol Number: RJ-CPX01 | Start Date*: 2017-07-21 | |||||||||||
Sponsor Name:Laboratorio Reig Jofre, SA | |||||||||||||
Full Title: Phase III, multicentre, randomised, double blind, parallel-group, clinical trial to evaluate the efficacy and safety of a new medicated nail lacquer for the treatment of toenail fungal infection | |||||||||||||
Medical condition: toenail onychomycosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
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