- Trials with a EudraCT protocol (54)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
54 result(s) found for: Candidiasis, Oral.
Displaying page 1 of 3.
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: 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: 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: 2022-001210-19 | Sponsor Protocol Number: RCT-VCA-22 | Start Date*: 2022-11-28 | |||||||||||
Sponsor Name:Abel García García | |||||||||||||
Full Title: Efficacy of the Vacucis Candida® autovaccine in the management of chronic oral candidiasis. Randomized triple-blind randomized clinical trial. | |||||||||||||
Medical condition: Chronic oral candidiasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (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: 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: 2009-016655-21 | Sponsor Protocol Number: P-090756-01 | Start Date*: 2010-04-30 | |||||||||||
Sponsor Name:Ferrer Internacional, S.A | |||||||||||||
Full Title: A Multi-Centre, Randomized, Placebo-controlled, Parallel-Group, Double-Blinded Study to Compare the Therapeutic Efficacy, Safety and Tolerability of 3 Single Vaginal Doses of Arasertaconazole Nitra... | |||||||||||||
Medical condition: Vulvovaginal Candidiasis | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: CZ (Completed) HU (Completed) FR (Completed) LT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2024-000382-25 | Sponsor Protocol Number: SCY-078-120 | Start Date*: 2024-09-25 | |||||||||||
Sponsor Name:SCYNEXIS, Inc. | |||||||||||||
Full Title: A Phase 1, Open-Label Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Oral Ibrexafungerp (SCY-078) in Adolescent Female Subjects | |||||||||||||
Medical condition: Vulvovaginal candidiasis | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001270-26 | Sponsor Protocol Number: VMT-VT-1161-CL-012 | Start Date*: 2018-12-12 | |||||||||||
Sponsor Name:Mycovia Pharmaceuticals, Inc | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of VT-1161 Oral Capsules in the Treatment of Subjects with Recurrent Vulvovaginal Candidiasis | |||||||||||||
Medical condition: Recurrent Vulvovaginal Candidiasis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: CZ (Completed) BE (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000371-32 | Sponsor Protocol Number: 13-02/AM-MG | Start Date*: 2014-10-06 | |||||||||||
Sponsor Name:Dermapharm AG | |||||||||||||
Full Title: Randomised, double-blind, vehicle controlled trial comparing Amphotericin B 100.000 I.E./g oral gel vs. Ampho-Moronal® suspension vs. modified vehicle to suspension in adult patients with oropharyn... | |||||||||||||
Medical condition: Oropharyngeal candidiasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000925-27 | Sponsor Protocol Number: ProF-001_Phase_IIb/III | Start Date*: 2019-08-27 | |||||||||||
Sponsor Name:Profem GmbH | |||||||||||||
Full Title: A phase IIb/III, parallel-arm, randomized, active-controlled, double-blind, double-dummy, study in patients with recurrent vulvovaginal candidiasis to compare the clinical efficacy, safety and tole... | |||||||||||||
Medical condition: recurrent vulvovaginal candidiasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: AT (Completed) SK (Completed) | |||||||||||||
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: 2008-000718-63 | Sponsor Protocol Number: 13071 | Start Date*: 2008-09-02 | |||||||||||
Sponsor Name:Bayer Consumer Care AG | |||||||||||||
Full Title: An investigator-blinded, active-controlled phase 3 study to prove the non-inferior efficacy of a Clotrimazole ovule (500 mg) versus a Clotrimazole vaginal tablet (500 mg) in vaginal candidiasis | |||||||||||||
Medical condition: vaginal candidiasis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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: 2016-002808-19 | Sponsor Protocol Number: 030(4C)HO16241 | Start Date*: 2017-10-11 | |||||||||||
Sponsor Name:A.C.R.A.F. S.p.A. (Aziende Chimiche Riunite Angelini Francesco) | |||||||||||||
Full Title: Phase III study to evaluate the efficacy of a novel antimycotic vaginal pessary combination (containing Benzydamine HCl 6 mg and Econazole nitrate 150 mg) in the Treatment of uncomplicated vulvovag... | |||||||||||||
Medical condition: Uncomplicated vulvovaginal candidosis (VVC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BG (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003784-56 | Sponsor Protocol Number: NV012013 | Start Date*: 2014-04-15 |
Sponsor Name:VUAB Pharma a.s. | ||
Full Title: An open, randomized, clinical trial parallel-controlled with Mycostatin oral suspension, evaluating the efficacy of Nystatin oral gel and Nystatin oral suspension in adult patients with oropharynge... | ||
Medical condition: Laboratory confirmed efficacy of Nystatin in pharmaceutical forms for buccal use, in patients with oropharyngeal candidiasis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-002600-40 | Sponsor Protocol Number: SCY-078-304 | Start Date*: 2020-01-17 | |||||||||||
Sponsor Name:SCYNEXIS, Inc. | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Oral Ibrexafungerp (SCY-078) Compared to Placebo in Subjects with Recurrent Vulvova... | |||||||||||||
Medical condition: Recurrent Vulvovaginal Candidiasis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: PL (Completed) BG (Completed) | |||||||||||||
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: 2010-021502-38 | Sponsor Protocol Number: LO-10-02 | Start Date*: 2011-01-25 | ||||||||||||||||
Sponsor Name:Christine Fromer Stiftung | ||||||||||||||||||
Full Title: STUDIE ZUR MESSUNG DER VAGINALEN INTERLEUKINE BEI PATIENTINNEN MIT ZERVIKALEN NEOPLASIEN (CIN 1-3) ODER CHRONISCHER CANDIDIASIS VAGINALIS UNTER BEHANDLUNG MIT 4PHENYL-BUTYRATE | ||||||||||||||||||
Medical condition: Patienten mit diagnostizierter cervikaler Neoplasie (CIN1-3) oder chronisch - rezidivierender Vaginalcandidiasis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
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 |
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