- Trials with a EudraCT protocol (14)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
14 result(s) found for: Mycology.
Displaying page 1 of 1.
EudraCT Number: 2006-000775-15 | Sponsor Protocol Number: TERBI 06/05 | Start Date*: 2006-09-11 |
Sponsor Name:PLIVA - ISTRAĊ½IVANJE I RAZVOJ d.o.o. | ||
Full Title: Double blind, comparative, randomized, placebo controlled, clinical study of therapeutic equivalence and tolerability of the topical preparation Terbinafine cream 1% (Pliva Croatia) with the medica... | ||
Medical condition: Uncomplicated Tinea pedis. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-001493-34 | Sponsor Protocol Number: OM01 | Start Date*: 2014-12-02 |
Sponsor Name:photonamic GmbH & Co. KG | ||
Full Title: Evaluation of the suitability of PD P 506 A in the photodynamic therapy of Distal Subungual Onychomycosis (DSO) of the great toenail. | ||
Medical condition: Onychomycosis (OM) is a chronic fungal infection of the finger- or toenails and one of the commonest dermatological conditions. It accounts for one third of fungal skin infections and constitutes a... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-001204-39 | Sponsor Protocol Number: MOB015B-III | Start Date*: 2016-09-15 | |||||||||||
Sponsor Name:Moberg Pharma AB (publ) | |||||||||||||
Full Title: A multi-centre, randomized, two-armed, parallel group and evaluator-blinded study of efficacy and safety of topical MOB015B in the treatment of mild to moderate distal subungual onychomycosis (DSO) | |||||||||||||
Medical condition: Distal Subungual Onychomycosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) PL (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001263-32 | Sponsor Protocol Number: 241011BS | Start Date*: 2006-07-21 |
Sponsor Name:York Pharma GmbH | ||
Full Title: Phase III study to evaluate the anti-mycotic efficacy of a topical Abafungin formulation in patients with tinea pedis | ||
Medical condition: Patients with tinea pedis interdigitalis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) DE (Completed) IS (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-005595-17 | Sponsor Protocol Number: PMPed-004 | Start Date*: 2014-02-11 | |||||||||||
Sponsor Name:Polichem S.A. | |||||||||||||
Full Title: Multicentre, open label study to assess the tolerability of P-3058 nail solution in paediatric patients affected by mild-to-moderate onychomycosis | |||||||||||||
Medical condition: Onychomycosis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) DE (Completed) BE (Completed) LV (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003570-10 | Sponsor Protocol Number: CSFO327N2303 | Start Date*: 2007-03-02 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, open-label, active-controlled, multicenter, parallel group study to assess the efficacy, safety and tolerability of topical 10% terbinafine hydrogen chloride (HCl) formulation versus ... | |||||||||||||
Medical condition: mild to moderate toenail onychomycosis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IS (Completed) FI (Completed) HU (Completed) ES (Completed) FR (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003508-21 | Sponsor Protocol Number: CSFO327N2302 | Start Date*: 2006-10-20 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, double-blind, vehicle-controlled, multicenter, parallel group study to assess the efficacy, safety, and tolerability of topical terbinafine hydrogen chloride (HCl) formulation for 24 ... | |||||||||||||
Medical condition: Onychomycosis (mild to moderate) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002949-11 | Sponsor Protocol Number: 601-0014 | Start Date*: 2019-08-05 | |||||||||||
Sponsor Name:Pulmatrix, Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Multi-Center, Placebo-Controlled Phase 2 Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Itraconazole Administered as a Dry Powder for Inhalation (PU... | |||||||||||||
Medical condition: Asthma with Allergic Bronchopulmonary Aspergillosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003506-25 | Sponsor Protocol Number: CSFO327N2301 | Start Date*: 2007-03-01 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, double-blind, vehicle-controlled, multicenter, parallel group study to assess the efficacy, safety, and tolerability of topical terbinafine hydrogen chloride (HCl) formulation for 24 ... | |||||||||||||
Medical condition: Onychomycosis (mild to moderate) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IS (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003106-41 | Sponsor Protocol Number: CHDR1733 | Start Date*: 2018-09-05 | |||||||||||
Sponsor Name:Maruho Co., Ltd. | |||||||||||||
Full Title: A phase 2, randomized, vehicle and ketoconazole-controlled, evaluator-blinded, study to explore the efficacy, pharmacodynamics and safety of omiganan 1.75% topical gel BID in patients with mild to ... | |||||||||||||
Medical condition: Mild to moderate facial seborrheic dermatitis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005275-10 | Sponsor Protocol Number: A1501080 | Start Date*: 2009-03-24 | |||||||||||||||||||||
Sponsor Name:Pfizer Inc, 235 East 42nd Street, New York, NY 10017 | |||||||||||||||||||||||
Full Title: A PROSPECTIVE, OPEN-LABEL, NON-RANDOMIZED, MULTI-CENTER STUDY TO INVESTIGATE THE SAFETY AND TOLERABILITY OF VORICONAZOLE AS PRIMARY THERAPY FOR TREATMENT OF INVASIVE ASPERGILLOSIS AND MOLDS SUCH AS... | |||||||||||||||||||||||
Medical condition: Treatment of proven or probable invasive aspergillosis (IA) and rare molds such as Scedosporium or Fusarium species. | |||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Completed) HU (Completed) CZ (Prematurely Ended) ES (Prematurely Ended) DE (Completed) BG (Prematurely Ended) Outside EU/EEA | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-018793-21 | Sponsor Protocol Number: CL-067-III-01 | Start Date*: 2010-05-05 | |||||||||||
Sponsor Name:Celtic Pharma Development Services Bermuda Limited | |||||||||||||
Full Title: A Randomized, Double-blind, Vehicle- and Placebo-Controlled, Multicenter Trial in Patients with Mild to Moderate Distal Subungual Toenail Onychomycosis to Investigate the Efficacy, Tolerability, an... | |||||||||||||
Medical condition: Clinically diagnosed distal subungual onychomycosis of the toenails caused by dermatophytes confirmed by positive mycology (culture and potassium hydroxide [KOH] visualization) (tinea unguium). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IS (Completed) DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014652-30 | Sponsor Protocol Number: SPK-843-03/01 | Start Date*: 2009-10-29 | |||||||||||||||||||||
Sponsor Name:PRO APARTS SRL | |||||||||||||||||||||||
Full Title: Efficacy, safety and pharmacokinetics of SPK-843 in the treatment of pulmonary mycosis.Phase III Open clinical study | |||||||||||||||||||||||
Medical condition: pulmonary mycosis(cryptococcosis o aspergillosis) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002289-33 | Sponsor Protocol Number: 601-0018 | Start Date*: 2023-02-01 | ||||||||||||||||
Sponsor Name:Pulmatrix, Inc. | ||||||||||||||||||
Full Title: A Randomized, Double-Blind, Multicenter, Placebo-Controlled Study to Evaluate the Effect of Dose and Duration of Treatment of Itraconazole Administered as a Dry Powder for Inhalation (PUR1900) on S... | ||||||||||||||||||
Medical condition: Allergic bronchopulmonary aspergillosis (ABPA) in patients with asthma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
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