- Trials with a EudraCT protocol (328)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
328 result(s) found for: psoriasis.
Displaying page 1 of 17.
EudraCT Number: 2014-004798-17 | Sponsor Protocol Number: CAIN457F2301T | Start Date*: 2015-05-26 | ||||||||||||||||
Sponsor Name:Universitätsklinikum Erlangen | ||||||||||||||||||
Full Title: Evaluation of inflammatory and structural joint damage in patients with psoriasis and psoriatic arthritis treated with secukinumab: A phase 2, single arm, single centre mode of action study (Psoria... | ||||||||||||||||||
Medical condition: Psoriasis or prosiatric arthritis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-002588-40 | Sponsor Protocol Number: CAIN457ADE02T | Start Date*: 2016-05-31 | |||||||||||
Sponsor Name:University Hospital Schleswig-Holstein | |||||||||||||
Full Title: Exploratory Evaluation of Biomarkers associated with Treatment Response to Cosentyx (Secukinumab) in Psoriasis Patients | |||||||||||||
Medical condition: moderate-to-severe psoriasis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
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: 2022-003477-36 | Sponsor Protocol Number: KKS-303 | Start Date*: 2023-06-27 | ||||||||||||||||
Sponsor Name:Justus-Liebig University Giessen - KKS Marburg-Giessen | ||||||||||||||||||
Full Title: Safety and immunogenicity of SHIngrix VAccination in patients suffering from Psoriasis or Psoriatic arthritis (SHIVAP) | ||||||||||||||||||
Medical condition: Psoriasis vulgaris and/or psoriatric arthritis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002141-39 | Sponsor Protocol Number: CDP870-040 | Start Date*: 2005-10-25 | |||||||||||
Sponsor Name:UCB Pharma S.A. | |||||||||||||
Full Title: Multicenter, dose response, randomized, double blin, parallel, 3 arms, placebo controlled clinical trial to evaluate the efficacy and the safety of subcutaneous CDP870 (certolizumab pegol) at 2 dif... | |||||||||||||
Medical condition: Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002446-36 | Sponsor Protocol Number: BP40635 | Start Date*: 2018-11-05 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: AN OPEN LABEL PHASE 2A TRIAL ASSESSING THE CLINICAL EFFICACY AND SAFETY OF RO5459072 IN MODERATE TO SEVERE PSORIASIS | |||||||||||||
Medical condition: Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016261-28 | Sponsor Protocol Number: H 521 000 - 0915 | Start Date*: 2010-01-26 | ||||||||||||||||
Sponsor Name:Almirall Hermal GmbH | ||||||||||||||||||
Full Title: Randomized, observer-blind, multi-center, reference-controlled phase IIb study to evaluate the efficacy of topically applied LAS41002 lotion in the treatment of scalp psoriasis | ||||||||||||||||||
Medical condition: Psoriasis vulgaris on the scalp | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-002532-24 | Sponsor Protocol Number: 0155/2018 | Start Date*: 2018-12-27 | |||||||||||
Sponsor Name:HELM AG | |||||||||||||
Full Title: A phase III, multicentre, randomised, double-blind, parallel-group trial to evaluate the efficacy and safety of a generic gel (calcipotriol + betamethasone 50 μg/g + 0.5 mg/g gel) compared to origi... | |||||||||||||
Medical condition: mild to moderate plaque-type psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002368-15 | Sponsor Protocol Number: PS0016 | Start Date*: 2016-11-15 | |||||||||||
Sponsor Name:UCB Biopharma SPRL | |||||||||||||
Full Title: A Multicenter, Randomized, Subject-Blind, Investigator-Blind Study to Evaluate the Time Course of Pharmacodynamic Response, Safety and Pharmacokinetics of Bimekizumab in Adult Subjects With Moderat... | |||||||||||||
Medical condition: Chronic Plaque Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
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: 2012-002998-62 | Sponsor Protocol Number: ROF-PSOR_104 | Start Date*: 2012-12-13 | |||||||||||
Sponsor Name:Takeda Pharma A/S | |||||||||||||
Full Title: A Randomized, Single-Center, Observer-Blind, Vehicle- and Active Comparator-Controlled Phase 1b Study to Assess the Effect and Local Safety and Tolerability Of Roflumilast and BYK321084 – Phosphod... | |||||||||||||
Medical condition: Mild to moderate, chronical, stable Psoriasis vulgaris | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (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: 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: 2007-007037-39 | Sponsor Protocol Number: BF-37-CT-002 | Start Date*: 2008-02-14 | |||||||||||
Sponsor Name:Biofrontera Bioscience GmbH | |||||||||||||
Full Title: A Phase II Proof-of-Concept, Randomized, Double-blind, Vehicle-controlled Study, Including an Open-label Comparison to an Active Control, To Assess the Efficacy and Safety/Tolerability of Topical R... | |||||||||||||
Medical condition: Patients with stable plaque-type psoriasis with plaques of sufficient size of at least 2 cm in diameter for five comparable treatment areas | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002934-57 | Sponsor Protocol Number: PS0018 | Start Date*: 2017-02-22 | |||||||||||
Sponsor Name:UCB Biopharma SPRL | |||||||||||||
Full Title: A multicenter, 48-week, open-label extension study to assess the long-term safety, tolerability, and efficacy of bimekizumab in adult subjects with moderate to severe chronic plaque psoriasis. | |||||||||||||
Medical condition: Chronic Plaque Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002212-16 | Sponsor Protocol Number: CAIN457ADE03 | Start Date*: 2015-01-22 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: Exploratory study on the kinetics of psoriasis symptoms, pruritus intensity and lesional biomarkers in patients with moderate to severe plaque-type psoriasis treated with subcutaneous secukinumab (... | |||||||||||||
Medical condition: chronic moderate to severe plaque type psoriasis | |||||||||||||
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Population Age: Adults, Elderly | 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: 2008-000197-20 | Sponsor Protocol Number: R013 | Start Date*: 2008-11-28 | |||||||||||
Sponsor Name:Revotar Biopharmaceuticals AG | |||||||||||||
Full Title: Multi-center, randomized, double-blind, placebo-controlled Phase 2 study to evaluate the safety and efficacy of Bimosiamose 5% Cream for the treatment of patients with chronic plaque type psoriasis | |||||||||||||
Medical condition: chronic plaque-type psoriasis (psoriasis vulgaris) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
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