- Trials with a EudraCT protocol (31)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
31 result(s) found for: Invasive candidiasis.
Displaying page 1 of 2.
EudraCT Number: 2008-006409-18 | Sponsor Protocol Number: 9463-EC-0002 | Start Date*: 2010-02-09 | ||||||||||||||||
Sponsor Name:Astellas Pharma Europe Ltd. | ||||||||||||||||||
Full Title: An Exploratory Study to Compare the Efficacy and Safety of Micafungin as a Pre-emptive Treatment of Invasive Candidiasis versus Placebo in High Risk Surgical Subjects - A Multicentre, Randomized, D... | ||||||||||||||||||
Medical condition: Invasive Candidiasis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) ES (Completed) HU (Completed) BE (Completed) GR (Completed) DE (Completed) FR (Completed) FI (Completed) IT (Completed) GB (Completed) DK (Completed) NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-014600-66 | Sponsor Protocol Number: IFN-gamma 001 | Start Date*: 2010-08-10 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:University Medical Center Nijmegen | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A multicentre, prospective, randomized open-label pilot study to assess the feasibility and preliminary efficacy of interferon gamma in combination with Anidulafungin for the treatment of candidemia | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Candida bloodstream infections/ candidemia | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-004504-36 | Sponsor Protocol Number: 801-00 | Start Date*: 2005-12-20 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Comparative Study to Evaluate the Safety, Tolerability, and Efficacy of 2 Dosing Regimens of Caspofungin in the Treatment of Invasive Candidiasis in Adults. | |||||||||||||
Medical condition: Candidiasis (invasive) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) BE (Completed) IT (Completed) PT (Completed) DE (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001491-39 | Sponsor Protocol Number: 03-0-192 | Start Date*: 2005-02-16 | |||||||||||
Sponsor Name:Astellas Pharma US, Inc. | |||||||||||||
Full Title: A PHASE 3, RANDOMIZED, DOUBLE-BLIND, COMPARATIVE STUDY OF MICAFUNGIN (FK463) VERSUS CASPOFUNGIN AS ANTIFUNGAL TREATMENT IN PATIENTS WITH INVASIVE CANDIDIASIS OR CANDIDEMIA | |||||||||||||
Medical condition: Invasive candidiasis or candidemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) GB (Completed) BE (Completed) AT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015159-26 | Sponsor Protocol Number: UKW-Inf-001 | Start Date*: 2011-03-14 | ||||||||||||||||||||||||||
Sponsor Name:Universitaetsklinikum Wuerzburg | ||||||||||||||||||||||||||||
Full Title: UKW-Inf-001: Prospective trial to evaluate pharmacokinetic, safety and efficacy of intermittent application of increased doses of caspofungin for antifungal prophylaxis in high risk patients. | ||||||||||||||||||||||||||||
Medical condition: Prophylaxis of invasive fungal infection, including life-threatening aspergillosis and candidiasis, is investigated in the study. Patient with acute myeloid leukemia or acute lymphatic leukemia wil... | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012848-16 | Sponsor Protocol Number: A1501085 | Start Date*: 2010-04-28 | |||||||||||||||||||||
Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, NY 10017, USA | |||||||||||||||||||||||
Full Title: A PROSPECTIVE, OPEN-LABEL, NON-COMPARATIVE STUDY TO ASSESS THE SAFETY, TOLERABILITY AND EFFICACY OF VORICONAZOLE FOR THE PRIMARY AND SALVAGE TREATMENT OF INVASIVE CANDIDIASIS, CANDIDEMIA, AND ESOPH... | |||||||||||||||||||||||
Medical condition: Invasive candidiasis, including candidemia (ICC), and esophageal candidiasis (EC) | |||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) HU (Prematurely Ended) SK (Completed) CZ (Prematurely Ended) BG (Completed) RO (Completed) Outside EU/EEA | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-000607-15 | Sponsor Protocol Number: GS-IT-131-0177 | Start Date*: 2007-12-06 | |||||||||||
Sponsor Name:GILEAD SCIENCES S.R.L. | |||||||||||||
Full Title: Phase II pilot multicenter study on efficacy and safety of liposomal amphotericin B (AmBisome) at 2 mg/kg/day in the treatment of candidemia and invasive candidiasis in nonneutropenic patients | |||||||||||||
Medical condition: CANDIDEMIA AND INVASIVE CANDIDIASIS | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016386-28 | Sponsor Protocol Number: ANIDULA-133 | Start Date*: 2010-01-05 | |||||||||||
Sponsor Name:University Medical Center Groningen | |||||||||||||
Full Title: Pharmacokinetics of critically ill patients with invasive candidiasis | |||||||||||||
Medical condition: invasive candidiasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000648-32 | Sponsor Protocol Number: SCY-078-302 | Start Date*: 2023-03-31 | ||||||||||||||||
Sponsor Name:SCYNEXIS, Inc. | ||||||||||||||||||
Full Title: A Phase 3, Multicenter, Prospective, Randomized, Double-blind Study of Two Treatment Regimens for Candidemia and/or Invasive Candidiasis: Intravenous Echinocandin followed by Oral Ibrexafungerp ver... | ||||||||||||||||||
Medical condition: Invasive Candidiasis/ Candidemia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GR (Trial now transitioned) FR (Trial now transitioned) ES (Temporarily Halted) BE (Trial now transitioned) BG (Trial now transitioned) IT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003793-13 | Sponsor Protocol Number: 2017_07 | Start Date*: 2018-03-22 | |||||||||||
Sponsor Name:centre hospitalier et universitaire de Lille | |||||||||||||
Full Title: Arrêt précoce du traitement antifongique empirique en réanimation guidé par dosages sériques de biomarqueurs fongiques : Etude randomisée contrôlée | |||||||||||||
Medical condition: INFECTION INVASIVE A CANDIDA | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004150-32 | Sponsor Protocol Number: A8851008 | Start Date*: 2008-11-18 | |||||||||||
Sponsor Name:Pfizer, Spain | |||||||||||||
Full Title: ESTUDIO PROSPECTIVO ABIERTO PARA EVALUAR LA FARMACOCINÉTICA, LA SEGURIDAD Y LA EFICACIA DE LA ANIDULAFUNGINA EN EL TRATAMIENTO DE NIÑOS Y ADOLESCENTES CON CANDIDIASIS INVASIVA, INCLUIDA LA CANDIDEM... | |||||||||||||
Medical condition: CANDIDIASIS INVASIVA, INCLUIDA CANDIDEMIA | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) FR (Completed) PT (Completed) IT (Completed) GR (Completed) Outside EU/EEA GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001566-26 | Sponsor Protocol Number: BDG-ETHIC | Start Date*: 2017-01-11 | |||||||||||
Sponsor Name:AOU DI BOLOGNA POLICLINICO S.ORSOLA-MALPIGHI | |||||||||||||
Full Title: A B-D-GLUCAN DRIVEN ANTIFUNGAL STEWARDSHIP APPROACH TO MANAGE EMPIRICAL THERAPY IN PATIENTS AT VERY HIGH RISK FOR INVASIVE CANDIDIASIS: A RANDOMIZED CONTROLLED TRIAL | |||||||||||||
Medical condition: invasive candidiasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004910-27 | Sponsor Protocol Number: MK-0991-074 | Start Date*: 2015-02-24 |
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | ||
Full Title: A Multicenter, Noncomparative, Open-label Study to Estimate the Safety, Efficacy, and Pharmacokinetics of MK-0991 (Caspofungin) in Japanese Children and Adolescents with Documented Candida or Asp... | ||
Medical condition: Candida or Aspergillus Infections | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2007-004854-97 | Sponsor Protocol Number: A8851019 | Start Date*: 2008-01-15 | |||||||||||
Sponsor Name:Pfizer Ltd | |||||||||||||
Full Title: OPEN-LABEL, NON-COMPARATIVE, STUDY OF INTRAVENOUS ANIDULAFUNGIN, FOLLOWED OPTIONALLY BY ORAL VORICONAZOLE OR FLUCONAZOLE THERAPY, FOR TREATMENT OF DOCUMENTED CANDIDEMIA/INVASIVE CANDIDIASIS IN INTE... | |||||||||||||
Medical condition: CANDIDAEMIA/INVASIVE CANDIDIASIS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) FR (Completed) BE (Completed) PT (Completed) NL (Completed) IT (Completed) SK (Completed) PL (Completed) CZ (Completed) DK (Completed) HU (Completed) DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002630-21 | Sponsor Protocol Number: CD101.IV.3.05 | Start Date*: 2019-01-10 | ||||||||||||||||
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 Intravenous Caspofungin Followed by Optional Oral Fluconazole Step-down in the... | ||||||||||||||||||
Medical condition: Candidemia; invasive candidiasis. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BG (Completed) DE (Completed) GR (Completed) FR (Completed) BE (Completed) IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002084-26 | Sponsor Protocol Number: MK0991-064 | Start Date*: 2017-01-27 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp. | |||||||||||||
Full Title: A Multicenter, Double-Blind, Randomized, Comparator-Controlled Study to Evaluate the Safety, Tolerability, and Efficacy of Caspofungin Versus Amphotericin B Deoxycholate in the Treatment of Invasiv... | |||||||||||||
Medical condition: Invasive Candidiasis | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Prematurely Ended) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003951-18 | Sponsor Protocol Number: WSA-CS-008 | Start Date*: 2007-05-29 | |||||||||||
Sponsor Name:Astellas Global Pharma Development, Inc. | |||||||||||||
Full Title: A phase III, double-blind, randomized study to evaluate the safety and efficacy of BAL8557 versus a Caspofungin followed by Voriconazole regimen in the treatment of candidemia and other invasive Ca... | |||||||||||||
Medical condition: Treatment of Candidemia and other invasive Candida infections | |||||||||||||
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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) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003617-34 | Sponsor Protocol Number: 41676 | Start Date*: 2013-01-30 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: Pharmacokinetics and optimal dosage of caspofungin in critically ill patients with suspected invasive candidiasis. | ||
Medical condition: suspected invasive candidiasis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-000424-32 | Sponsor Protocol Number: 045 | Start Date*: 2004-09-23 |
Sponsor Name:Merck Sharp & Dohme BV | ||
Full Title: A Multicenter, Open, Noncomparative Study to Estimate the Safety, Tolerability, and Efficacy of Caspofungin Acetate in the Treatment of Adults with Invasive Candida Infections (Excluding Patients w... | ||
Medical condition: Non-Blood Invasive Candidiasis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
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 |
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