- Trials with a EudraCT protocol (23)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (27)
23 result(s) found for: Lacquer.
Displaying page 1 of 2.
EudraCT Number: 2006-006569-18 | Sponsor Protocol Number: V00074 VE 202 04A | Start Date*: 2007-03-16 | |||||||||||
Sponsor Name:PIERRE FABRE DERMATOLOGIE represented by INSTITUT DE RECHERCHE PIERRE FABRE | |||||||||||||
Full Title: EFFICACY AND SAFETY OF 8% CLOBETASOL NAIL LACQUER FORMULATION VERSUS VEHICLE IN NAIL PSORIASIS | |||||||||||||
Medical condition: NAIL PSORIASIS | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000544-26 | Sponsor Protocol Number: RD.03.SPR.29106 | Start Date*: 2013-12-10 | |||||||||||
Sponsor Name:Galderma R&D | |||||||||||||
Full Title: Determination of antifungal activity of Loceryl® Nail Lacquer 5% when used concomitantly with a cosmetic nail varnish compared to a Loceryl® Nail Lacquer 5% alone in treatment of toenail Distal Sub... | |||||||||||||
Medical condition: Mild to moderate toenail Distal Subungual Onychomycosis | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IS (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: 2015-001237-24 | Sponsor Protocol Number: RD.03.SPR.105082 | Start Date*: 2015-07-28 | |||||||||||
Sponsor Name:Galderma R&D | |||||||||||||
Full Title: Subject adherence and satisfaction for treatment of Onychomycosis with Loceryl® Nail Lacquer 5% versus Ciclopoli® Nail Lacquer. | |||||||||||||
Medical condition: Toenail Distal and Lateral Subungual Onychomycosis | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005895-42 | Sponsor Protocol Number: TLT-CLI-001 | Start Date*: 2009-03-02 | |||||||||||
Sponsor Name:TLT Medical Ltd. | |||||||||||||
Full Title: A study to determine the safety and efficacy of a terbinafine topical formulation system in subjects with onychomycosis in laser treated toenails versus ciclopirox lacquer in intact toenails | |||||||||||||
Medical condition: Distal/lateral Subungual onychomycosis (DSO) caused by dermatophytes | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IS (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000974-54 | Sponsor Protocol Number: RD.03.SPR.40026 | Start Date*: 2007-02-28 | |||||||||||
Sponsor Name:GALDERMA Research & Development | |||||||||||||
Full Title: A multi-centre, randomized, parallel groups, vehicle and active controlled study of amorolfine 4% and 10% nail lacquer new formulation in the topical treatment of distal and lateral subungual toena... | |||||||||||||
Medical condition: Distal and lateral subungual onychomycosis | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IS (Completed) CZ (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004825-87 | Sponsor Protocol Number: R00002 VE 201 | Start Date*: 2005-04-22 | |||||||||||
Sponsor Name:Pierre Fabre Dermatologie represented by Institut de Recherche Pierre Fabre | |||||||||||||
Full Title: Efficacy and safety of 0,1%, 0,5% and 1% TAZAROTENE nail lacquer formulation versus vehicle in nail psoriasis. International, multicenter, double-blind, randomized study of four parallel groups. | |||||||||||||
Medical condition: Psoriasis of the skin is frequently accompanied by nail changes: between 10 and 78% of psoriatic patients suffer from changes of the nails. More than 50% of patients with nail psoriasis have pain b... | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) DE (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001503-31 | Sponsor Protocol Number: RD.03.SPR.105078 | Start Date*: 2015-11-30 | |||||||||||
Sponsor Name:Galderma R&D | |||||||||||||
Full Title: Subject adherence and satisfaction for treatment of Onychomycosis with Loceryl® Nail Lacquer 5% versus Canesten® Fungal Nail Treatment Set | |||||||||||||
Medical condition: Mycological confirmed toenail Distal and Lateral Subungual Onychomycosis | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IS (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017642-32 | Sponsor Protocol Number: Nyreprofylakse1 | Start Date*: 2010-02-16 |
Sponsor Name:Odense University Hospital | ||
Full Title: Nyreprofylakse ved ST-segment elevation myokardie infarkt og primær PCI | ||
Medical condition: Decreased renal function in patients with STEMI undergoing acute PCI | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (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 | |||||||||||||
|
|||||||||||||
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: 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 | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-003913-12 | Sponsor Protocol Number: 22/589-EC_M. | Start Date*: 2023-03-07 |
Sponsor Name:COMPLUTENSE UNIVERSITY OF MADRID | ||
Full Title: Diode laser and photodynamic therapy Versus Ciclopirox Hydroxypropyl Chitosan. Randomised controlled clinical trial. | ||
Medical condition: Onychomycosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-011125-14 | Sponsor Protocol Number: RV4104A-2008-548 | Start Date*: 2009-07-06 | |||||||||||
Sponsor Name:Pierre Fabre Dermatologie | |||||||||||||
Full Title: A multicentre, randomized, controlled study of the efficacy, safety and cost-effectiveness of a sequential therapy with RV4104A ointment, ciclopiroxolamine cream and ciclopirox film-forming solutio... | |||||||||||||
Medical condition: Patients suffering from distal-lateral or lateral subungual onychomycosis of one great toenail (the target nail) without matrix involvement | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002707-10 | Sponsor Protocol Number: PM0731 | Start Date*: 2009-03-04 | |||||||||||
Sponsor Name:Polichem SA | |||||||||||||
Full Title: MULTICENTRE, RANDOMIZED, DOUBLE BLIND WITHIN FREQUENCY OF ADMINISTRATION, PLACEBO CONTROLLED, DOSE-FINDING, PARALLEL-GROUP, EFFICACY AND SAFETY STUDY OF 3 DOSES OF P-3058 NAIL LACQUER (5% o.d., 10%... | |||||||||||||
Medical condition: Mild to moderate distal subungual Onychomycosis due to Dermatophytes. | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) LV (Completed) IT (Completed) FR (Completed) PL (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 | |||||||||||||
|
|||||||||||||
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: 2007-004331-27 | Sponsor Protocol Number: P05205 | Start Date*: 2008-12-23 | |||||||||||
Sponsor Name:Schering-Plough Research Institute, a Division of Schering Corporation | |||||||||||||
Full Title: A Randomized, Double-Blind, Vehicle-Controlled, Multicenter Study to Evaluate the Safety and Efficacy of SCH 900340 5% Solution Compared with Vehicle Administered Topically in the Treatment of Dist... | |||||||||||||
Medical condition: Onychomycosis | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) IS (Prematurely Ended) BE (Completed) SE (Prematurely Ended) ES (Prematurely Ended) GB (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003334-33 | Sponsor Protocol Number: CRFB002FIT01 | Start Date*: 2013-12-16 | |||||||||||
Sponsor Name:NOVARTIS FARMA | |||||||||||||
Full Title: A 12-month, open-label, interventional, multicentre study to investigate the current criteria driving re-treatment with ranibizumab upon relapse in patients with visual impairment due to choroidal ... | |||||||||||||
Medical condition: Choroidal neovascularization secondary to pathologic myopia | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002427-90 | Sponsor Protocol Number: SD-AMO-00326-08 | Start Date*: 2008-10-20 | |||||||||||
Sponsor Name:SUBSTIPHARM Développement | |||||||||||||
Full Title: Etude en double aveugle de l’équivalence clinique et mycologique du Locéryl® (Amorolfine, solution filmogène à 5%) et de son générique dans le traitement des onychomycoses sans atteinte de la matr... | |||||||||||||
Medical condition: Tout patient présentant une onychomycose unguéale sans atteinte matricielle d’un doigt ou d’un orteil n’ayant jamais encore été traité par un antimycosique | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021662-30 | Sponsor Protocol Number: CRFB002F2301 | Start Date*: 2010-11-05 | |||||||||||||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||||||||||||
Full Title: A 12 month, phase III, randomized, double-masked, multi-center, active-controlled study to evaluate the efficacy and safety of two different dosing regimens of 0.5 mg ranibizumab vs. verteporfin PD... | |||||||||||||||||||||||
Medical condition: visual impairment due to choroidal neovascularization secondary to pathologic myopia | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: PT (Completed) LV (Completed) HU (Completed) LT (Completed) FR (Completed) ES (Completed) IT (Completed) AT (Completed) SK (Completed) DE (Completed) GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-002365-34 | Sponsor Protocol Number: PM1434 | Start Date*: 2015-10-08 | |||||||||||
Sponsor Name:Polichem S.A. | |||||||||||||
Full Title: A RANDOMIZED, DOUBLE-BLIND, VEHICLE-CONTROLLED, PARALLEL-GROUP TRIAL TO ASSESS THE EFFICACY, SAFETY AND TOLERABILITY OF P-3073 FOR TOPICAL TREATMENT OF NAIL PSORIASIS | |||||||||||||
Medical condition: Mild to moderate psoriatic fingernail/s | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) DE (Completed) CZ (Completed) PL (Completed) BG (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
