- Trials with a EudraCT protocol (328)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (41)
328 result(s) found for: psoriasis.
Displaying page 3 of 17.
EudraCT Number: 2012-005288-29 | Sponsor Protocol Number: P1204LT | Start Date*: 2013-06-07 | |||||||||||
Sponsor Name:G. Pohl-Boskamp GmbH & Co. KG | |||||||||||||
Full Title: A single-center randomized, active-controlled, observer-blinded, parallel group trial to evaluate the efficacy and safety of a topical dimeticone formulation (Loion®) compared to 10% saliclylic aci... | |||||||||||||
Medical condition: psoriatic plaques in patients with chronic psoriasis capitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000335-27 | Sponsor Protocol Number: EPos | Start Date*: 2018-10-17 | |||||||||||
Sponsor Name:Universitätsklinikum Erlangen | |||||||||||||
Full Title: Early PsA on treatment strategy | |||||||||||||
Medical condition: Psoriasis vulgaris | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005512-21 | Sponsor Protocol Number: M20-326 | Start Date*: 2021-07-06 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Phase 3b Multicenter, Randomized, Open Label, Efficacy Assessor-Blinded Study of Risankizumab Compared to Apremilast for the Treatment of Adult Subjects with Moderate Plaque Psoriasis who are Can... | |||||||||||||
Medical condition: Moderate plaque psoriasis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004246-15 | Sponsor Protocol Number: CAIN457FDE04 | Start Date*: 2020-08-27 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A 28-week, randomized, double-blind, active-controlled, multicenter study to evaluate the efficacy of subcutaneously administered secukinumab compared to ustekinumab in adult patients with psoriati... | |||||||||||||
Medical condition: Psoriatic arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004022-15 | Sponsor Protocol Number: ANB019-003 | Start Date*: 2020-04-21 | |||||||||||
Sponsor Name:AnaptysBio Inc | |||||||||||||
Full Title: A Phase 2, Randomized, Placebo-controlled, Double-blind, Multiple Dose Study to Evaluate the Efficacy and Safety of ANB019 in Subjects with Palmoplantar Pustulosis | |||||||||||||
Medical condition: Palmoplantar pustulosis (PPP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003209-22 | Sponsor Protocol Number: UNI50001-203 | Start Date*: 2022-02-09 | |||||||||||
Sponsor Name:UNION therapeutics A/S | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Phase 2b Dose-Ranging Study to Evaluate the Efficacy and Safety of Orismilast in Adults with Moderate-to-Severe Plaque-Type Psoriasis | |||||||||||||
Medical condition: 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: 2020-004081-19 | Sponsor Protocol Number: 20-01/BetaSal-S | Start Date*: 2021-12-22 | |||||||||||
Sponsor Name:Dermapharm AG | |||||||||||||
Full Title: Double-blind, randomised clinical study comparing efficacy and safety of Betamethasone dipropionate 0.64 mg/g _ Salicylic acid 30 mg/g Ointment (Test) vs. Diprosalic(R) Ointment (Reference) vs. Veh... | |||||||||||||
Medical condition: Chronic stable plaque psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002098-40 | Sponsor Protocol Number: LP0133-1182 | Start Date*: 2016-02-10 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: A Phase 2a, Proof of Concept Trial, testing twice daily application of LEO 124249 ointment 30mg/g in the treatment of mild to moderate inverse psoriasis | |||||||||||||
Medical condition: inverse psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002793-39 | Sponsor Protocol Number: 0451 | Start Date*: 2018-03-13 | |||||||||||
Sponsor Name:Universitätsklinikum Erlangen | |||||||||||||
Full Title: Abatacept Bone Effects in Psoriatic Arthritis with Bone Biomarker – ABEPSA_BB | |||||||||||||
Medical condition: Psoriatic arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004254-22 | Sponsor Protocol Number: PASTOR2018 | Start Date*: 2020-03-20 | ||||||||||||||||
Sponsor Name:Charite University | ||||||||||||||||||
Full Title: Efficacy of Tofacitinib in Reduction of Inflammation Detected on MRI in Patients with Psoriatic ArthritiS PresenTing with Axial InvOlvement - a Randomized, Double-Blind, Placebo-Controlled, Mult... | ||||||||||||||||||
Medical condition: Psoriatic Arthritis with axial (spinal) involvement | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-005258-20 | Sponsor Protocol Number: CAIN457ADE06 | Start Date*: 2015-03-13 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A 24-week, randomized, controlled, multicenter, open-label study with blinded assessment of the efficacy of subcutaneous secukinumab compared to Fumaderm® in adults with moderate to severe plaque p... | |||||||||||||
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: 2007-005035-29 | Sponsor Protocol Number: VAL-010 | Start Date*: 2007-11-12 | |||||||||||
Sponsor Name:Valderm ApS | |||||||||||||
Full Title: A 13 day placebo- and reference-controlled, double-blind, monocentric, randomized, intraindividual comparative clinical phase IIa study, investigating the efficacy and tolerability of valrubicin cr... | |||||||||||||
Medical condition: Mild to Moderate Plaque Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018355-10 | Sponsor Protocol Number: H553000-1001 | Start Date*: 2010-06-18 | |||||||||||
Sponsor Name:Almirall Hermal GmbH | |||||||||||||
Full Title: An Investigator-blind, Controlled Study to Assess the Efficacy of Five Distinct Combinations of LAS 41004 in Different Concentrations Compared to Placebo and to Two Active Controls in a Psoriasis-P... | |||||||||||||
Medical condition: Plaque-type psoriasis (psoriasis vulgaris) for at least 6 months | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022281-27 | Sponsor Protocol Number: H553000-1005 | Start Date*: 2010-12-20 | |||||||||||
Sponsor Name:Almirall Hermal GmbH | |||||||||||||
Full Title: An Investigator-blind, Controlled Study to Assess the Efficacy and Safety of different formulations of LAS 41004 Compared to Placebo and to Active Control in a Psoriasis-Plaque-Test | |||||||||||||
Medical condition: Plaque-type psoriasis (psoriasis vulgaris) for at least 6 months | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003802-14 | Sponsor Protocol Number: CRC-PSO-SKINPEN-A-27 | Start Date*: 2016-11-25 | |||||||||||
Sponsor Name:Charité - Universitätsmedizin Berlin | |||||||||||||
Full Title: Skin penetration of anti-inflammatory compounds in lesional compared to non-lesional skin of psoriasis patients | |||||||||||||
Medical condition: Psoriasis vulgaris | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002795-96 | Sponsor Protocol Number: CBFH772A2201 | Start Date*: 2008-12-11 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A single center, phase I, partially blinded, placebo-controlled, first-in-man study to evaluate the safety, tolerability and Proof of Mechanism (PoM) of a single administration of BFH772 in healthy... | |||||||||||||
Medical condition: Plaque psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002649-69 | Sponsor Protocol Number: I1F-EW-RHBZ | Start Date*: 2015-12-09 | |||||||||||
Sponsor Name:Eli Lilly and Company Limited | |||||||||||||
Full Title: A 24-Week Multicenter, Randomized, Open-Label, Parallel Group Study Comparing the Efficacy and Safety of Ixekizumab to Fumaric Acid Esters and Methotrexate in Patients with Moderate-to-Severe Plaqu... | |||||||||||||
Medical condition: Moderate-to-Severe Plaque Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005777-20 | Sponsor Protocol Number: TMP-1115_01 | Start Date*: 2016-12-12 | |||||||||||
Sponsor Name:Fraunhofer Gesellschaft for its Institute Fraunhofer Institute for Translational Medicine and Pharmacology ITMP | |||||||||||||
Full Title: Impact of concomitant Methotrexate on efficacy, safety and adherence of Ustekinumab-treatment in patients with active Psoriatic Arthritis (MUST-Study) | |||||||||||||
Medical condition: active psoriatic arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005518-16 | Sponsor Protocol Number: U3P | Start Date*: 2021-05-10 | |||||||||||
Sponsor Name:Universitätsklinikum Erlangen | |||||||||||||
Full Title: U3P study - Upadacitinib in Psoriatic Arthritis Pain Processing | |||||||||||||
Medical condition: Psoriatic 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: 2011-000815-15 | Sponsor Protocol Number: BOS-1168-WEI-0080-I | Start Date*: 2011-08-02 |
Sponsor Name:Medizinische Fakultät der technischen Universität Muenchen | ||
Full Title: BOSTRIP (Investigator Initiated Trial) (Biomarkers of systemic treatment response in Psoriasis) Differential analysis of metabolomic profiles in patients with chronic plaque psoriasis underg... | ||
Medical condition: Psoriasis is a chronic hyperproliferative and inflammatory skin disease with its major subtype, chronic plaque-type psoriasis, affecting approximately 2% of individuals in Western populations. It m... | ||
Disease: | ||
Population Age: Elderly | Gender: | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
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