- Trials with a EudraCT protocol (156)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
156 result(s) found for: Psoriasis vulgaris.
Displaying page 1 of 8.
EudraCT Number: 2008-006004-36 | Sponsor Protocol Number: ACE-PSORIASIS-1 | Start Date*: 2008-12-16 | |||||||||||
Sponsor Name:ACE ApS | |||||||||||||
Full Title: Efficacy and tolerability of captopril ointment 0,1%, 0,3% and 1,0% in psoriasis vulgaris. A randomised, double-blind, placebocontrolled, doseescalating, intra-individual clinical study | |||||||||||||
Medical condition: Patients with psoriasis vulgaris | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000556-95 | Sponsor Protocol Number: LP0053-1004 | Start Date*: 2017-01-03 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: LEO 90100 twice weekly maintenance regimen for psoriasis vulgaris | |||||||||||||
Medical condition: Psoriasis vulgaris | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) FR (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006026-25 | Sponsor Protocol Number: DK040CP | Start Date*: 2007-03-16 | |||||||||||
Sponsor Name:Coloplast A/S, Consumer Products | |||||||||||||
Full Title: Psoriasis Investigation of 4 different treatment regimes | |||||||||||||
Medical condition: Psoriasis vulgaris | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-010863-18 | Sponsor Protocol Number: NL26548.101.09 | Start Date*: 2010-06-25 | |||||||||||||||||||||
Sponsor Name:Amphia ziekenhuis | |||||||||||||||||||||||
Full Title: The additive effect of short contact tar-derivates to UVB therapy in “en plaque” psoriasis: a prospective single blind unicenter randomized clinical trial | |||||||||||||||||||||||
Medical condition: Psoriasis patient getting UVB lighttherapy in a dermatological daycare center | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001630-14 | Sponsor Protocol Number: DRN0307 | Start Date*: 2007-10-30 | |||||||||||
Sponsor Name:University Medical Centre St. Radboud, Department of Dermatology | |||||||||||||
Full Title: Safety and efficacy of efalizumab in combination with methotrexate in patients with severe psoriasis: a comparative study. | |||||||||||||
Medical condition: Moderate to severe chronic plaque psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-007069-35 | Sponsor Protocol Number: 301106 | Start Date*: 2007-01-22 | |||||||||||
Sponsor Name:University Medical Centre St Radboud, Department of Dermatology | |||||||||||||
Full Title: Evaluation of Neodymium YAG laser-treatment compared to topical treatment with betamethasondipropionaat/calcipotriol ointment (Dovobet) for patients with chronic plaque type psoriasis | |||||||||||||
Medical condition: Chronic localized Psoriasis vulgaris | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000943-17 | Sponsor Protocol Number: NL54557.091.15 | Start Date*: 2016-02-11 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Radboudumc | ||||||||||||||||||||||||||||||||||||||
Full Title: Tight control dose reductions of biologics in psoriasis patients with low disease activity: a randomized pragmatic trial. | ||||||||||||||||||||||||||||||||||||||
Medical condition: Adult Patients diagnosed psoriasis vulgaris | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-017858-12 | Sponsor Protocol Number: LEO 22811-S22 | Start Date*: 2010-05-11 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: A phase 2a proof of concept study comparing three doses of an oral solution of LEO 22811 with a placebo oral solution for the treatment of psoriasis vulgaris | |||||||||||||
Medical condition: Psoriasis vulgaris | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000462-21 | Sponsor Protocol Number: 266-02/06 (AVT-02/2/PSO/02) | Start Date*: 2008-01-15 | |||||||||||
Sponsor Name:Avontec GmbH | |||||||||||||
Full Title: A multicenter, randomized, double-blind, placebo-controlled, intraindividual-comparison phase IIa trial to evaluate the efficacy and safety of 2% AVT-02 UE ointment in the treatment of mild to mode... | |||||||||||||
Medical condition: psoriasis vulgaris | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002765-31 | Sponsor Protocol Number: 066-007/08 (AVT-02/2/PSO/03) | Start Date*: 2008-06-18 | |||||||||||
Sponsor Name:Avontec GmbH | |||||||||||||
Full Title: A multicenter, randomized, double-blind, placebo-controlled, intraindividual-comparison phase IIa trial to evaluate the efficacy and safety of 2% AVT-02 UE ointment in an every other day treatment ... | |||||||||||||
Medical condition: psoriasis vulgaris | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002317-40 | Sponsor Protocol Number: 280210BS | Start Date*: 2008-10-17 | |||||||||||
Sponsor Name:Perrigo Israel Pharmaceuticals Ltd. | |||||||||||||
Full Title: A phase IIa, multi-center, randomized, double-blind, vehicle-controlled study to determine antipsoriatic efficacy and safety of topical CEP-701 (lestaurtinib) cream formulations in patients with ps... | |||||||||||||
Medical condition: Chronic plaque type psoriasis of mild to moderate severity, at least one plaque with a treatment area of approximately 25 - 50 cm2 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001126-90 | Sponsor Protocol Number: H 1000 2925-06/08 | Start Date*: 2006-07-06 | |||||||||||
Sponsor Name:Hermal Kurt Herrmann GmbH & Co. OHG | |||||||||||||
Full Title: Evaluation of safety and efficacy of Curatoderm® Emulsion in the treatment of patients with mild to moderate plaque psoriasis | |||||||||||||
Medical condition: Patients with mild to moderate plaque type Psoriasis vulgaris. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010963-18 | Sponsor Protocol Number: LEO80190-O25 | Start Date*: 2009-09-29 | |||||||||||
Sponsor Name:LEO Pharmaceutical Products Ltd. A/S (LEO Pharma A/S) | |||||||||||||
Full Title: A phase 3 study comparing an ointment containing calcipotriol 25 mcg/g plus hydrocortisone 10 mg/g (LEO 80190 ointment) with hydrocortisone 10 mg/g ointment, both applied once daily in the treatmen... | |||||||||||||
Medical condition: Psoriasis vulgaris on the face and on the intertriginous areas. | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003215-78 | Sponsor Protocol Number: MBL 0202 INT | Start Date*: 2005-11-16 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: Calcipotriol plus Betamethasone Dipropionate Gel Compared to Betamethasone Dipropionate in the Gel Vehicle, Calcipotriol in the Gel Vehicle and the Gel Vehicle alone in Psoriasis Vulgaris. | |||||||||||||
Medical condition: Psoriasis vulgaris on the trunk and/or limbs | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) IE (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000685-12 | Sponsor Protocol Number: MC2-01-C6 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:MC2 Therapeutics Ltd | |||||||||||||
Full Title: A Multicentre, Open-label, Single-group Maximal Use Trial, Evaluating the Safety and Pharmacokinetic Profile of the Active Ingredients and their Metabolites after application of MC2-01 Cream in Ado... | |||||||||||||
Medical condition: Extensive Psoriasis Vulgaris | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) CZ (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000106-37 | Sponsor Protocol Number: 37.07.-92906 | Start Date*: 2008-08-28 | |||||||||||
Sponsor Name:Klinik für Dermatologie und Allergologie der RUB, St. Josef Hospital | |||||||||||||
Full Title: Studies on the combined treatment using etanercept and ultraviolet B for patients with moderate to severe psoriasis vulgaris | |||||||||||||
Medical condition: Psoriasis vulgaris (Plaque-Typ) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000253-30 | Sponsor Protocol Number: LP0075-34 | Start Date*: 2012-11-08 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: An exploratory study evaluating the efficacy of cromoglicate cream compared to cream vehicle in the treatment of itch in psoriasis | |||||||||||||
Medical condition: itchy psoriasis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005279-25 | Sponsor Protocol Number: LP0058-1072 | Start Date*: 2016-06-22 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: LEO 32731 for the Treatment of Moderate to Severe Psoriasis Vulgaris A phase 2a proof of concept study comparing an oral tablet formulation of LEO 32731 with a corresponding placebo tablet in pati... | |||||||||||||
Medical condition: Psoriasis Vulgaris | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002141-24 | Sponsor Protocol Number: H 527000 - 0805 | Start Date*: 2008-05-26 | |||||||||||
Sponsor Name:Almirall Hermal GmbH | |||||||||||||
Full Title: A phase II, single-center, randomized, controlled, observer-blind study to determine the non-inferiority of a topical mometasone formulation vs a marketed comparator by evaluation of the anti-psori... | |||||||||||||
Medical condition: volunteers with psoriasis vulgaris in a cronic stable phase and stable plaques with an area sufficient for 3 treatment fields | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007525-39 | Sponsor Protocol Number: CAIN457A2211 | Start Date*: 2009-08-26 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, double-blind, placebo controlled, multicenter regimen finding study of subcutaneously administered AIN457, assessing Psoriasis Area and Severity Index (PASI) response in patients with... | |||||||||||||
Medical condition: Moderate to severe plaque-type psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IS (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
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