- Trials with a EudraCT protocol (7)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
7 result(s) found for: Onycholysis.
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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 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019706-16 | Sponsor Protocol Number: PM0812 | Start Date*: 2010-07-27 | |||||||||||
Sponsor Name:POLICHEM | |||||||||||||
Full Title: A randomized, double blind, placebo controlled, parallel groups, pilot study to assess the effects of two new nail lacquers, cyclosporine 5% and calcipotriol 0.005%, in the treatment of nail psoriasis | |||||||||||||
Medical condition: Nail psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) LV (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... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) DE (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006338-17 | Sponsor Protocol Number: CL-067-II-01 | Start Date*: 2007-08-22 | |||||||||||
Sponsor Name:CPDS BERMUDA, LTD. | |||||||||||||
Full Title: OPEN-LABEL STUDY OF EFFICACY AND SAFETY OF 067 (TERBINAFINE IN TRANSFERSOME®) FOR THE TREATMENT OF ONYCHOMYCOSIS | |||||||||||||
Medical condition: Bilateral onychomycosis of the hallux nail (great toe) with positive mycosis culture and KOH microscopy as per central laboratory, otherwise healthy according to physical examination | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002788-88 | Sponsor Protocol Number: 20190529 | Start Date*: 2021-01-11 | |||||||||||
Sponsor Name:Amgen Inc. | |||||||||||||
Full Title: A Phase 3, Multicenter, Double-blind, Randomized, Placebo-controlled, Parallel Group Study to Evaluate the Efficacy, Safety and Pharmacokinetics of Apremilast in Children From 5 to Less Than 18 Yea... | |||||||||||||
Medical condition: Juvenile psoriatic arthritis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Trial now transitioned) BE (Trial now transitioned) FR (Trial now transitioned) NL (Trial now transitioned) IT (Trial now transitioned) PL (Trial now transitioned) GR (Trial now transitioned) PT (Trial now transitioned) LT (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000699-32 | Sponsor Protocol Number: EU-0208/REMICADEPSO1006 | Start Date*: 2011-09-28 | |||||||||||
Sponsor Name:UZ KULeuven, service of Rheumatology | |||||||||||||
Full Title: Nail involvement in psoriatic arthritis: a cross-sectional and observational prospective study. | |||||||||||||
Medical condition: psoriatic artritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002850-58 | Sponsor Protocol Number: CC-10004-PSOR-020 | Start Date*: 2019-02-19 | |||||||||||
Sponsor Name:Amgen Inc. | |||||||||||||
Full Title: A PHASE 4, MULTI-CENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY OF THE IMPACT OF APREMILAST (CC-10004) ON QUALITY OF LIFE, EFFICACY, AND SAFETY IN SUBJECTS WITH MANIFESTATIONS OF PLAQUE... | |||||||||||||
Medical condition: Plaque Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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