- Trials with a EudraCT protocol (614)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (41)
614 result(s) found for: Psoriasis.
Displaying page 1 of 31.
| 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: 2009-010863-18 | 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: 2013-000164-28 | Sponsor Protocol Number: 8400-201 | Start Date*: 2013-04-04 | |||||||||||||||||||||
| Sponsor Name:Idera Pharmaceuticals, Inc. | |||||||||||||||||||||||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled, 12-week Dose-Ranging Trial of IMO-8400 in Patients with Moderate to Severe Plaque Psoriasis | |||||||||||||||||||||||
| Medical condition: Moderate to Severe Plaque Psoriasis | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2006-003252-38 | Sponsor Protocol Number: Hx-Inflam-302 | Start Date*: 2006-09-01 | |||||||||||
| Sponsor Name:Genmab A/S | |||||||||||||
| Full Title: An open label clinical pilot study with local injection of human antibody (HuMax-Inflam) for the treatment of inflammatory psoriasis | |||||||||||||
| Medical condition: inflammatory psoriasis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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: 2011-000571-13 | Sponsor Protocol Number: VIC-PSO1 | Start Date*: 2011-05-24 | |||||||||||
| Sponsor Name:Gentofte Hospital | |||||||||||||
| Full Title: The effect of GLP-1 in psoriasis | |||||||||||||
| Medical condition: Psoriasis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-004260-31 | Sponsor Protocol Number: HUM-05-096 | Start Date*: 2007-02-21 | |||||||||||
| Sponsor Name:UHL NHS Trust | |||||||||||||
| Full Title: An open label study of humira (adalimumab)in the treatment of patients with severe psoriasis | |||||||||||||
| Medical condition: Psoriasis | |||||||||||||
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| Population Age: | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-014364-18 | Sponsor Protocol Number: 579/09 | Start Date*: 2009-10-01 | |||||||||||
| Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
| Full Title: PSORIASIS AND CARDIOVASCULAR DISEASE: IMMUNOMODULATOR ROLE OF THE TREATMENT WITH ROSUVASTATIN IN PATIENTS WITH PSORIASIS OF MILD OR OF MODERATE-SEVERE SKIN DISEASE. | |||||||||||||
| Medical condition: PSORIASIS | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-007011-24 | Sponsor Protocol Number: 1583 | Start Date*: 2007-09-21 | |||||||||||
| Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
| Full Title: Assessment of endothelial function in patients with psoriasis before and after Etanercept treatment | |||||||||||||
| Medical condition: moderate to severe psoriasis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-003086-34 | Sponsor Protocol Number: CAIN457A3301 | Start Date*: 2013-12-04 | ||||||||||||||||
| Sponsor Name:Novartis Pharma Services AG | ||||||||||||||||||
| Full Title: A 52-week, multicenter, randomized, double-blind, placebo-controlled study of subcutaneous secukinumab to demonstrate efficacy as assessed by palmoplantar pustulosis Psoriasis Area and Severity Ind... | ||||||||||||||||||
| Medical condition: Moderate to severe chronic palmoplantar pustular psoriasis | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: SE (Completed) GB (Completed) AT (Completed) ES (Completed) DE (Completed) BE (Completed) IT (Completed) PL (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2016-002143-42 | Sponsor Protocol Number: 16013 | Start Date*: 2017-11-08 | |||||||||||
| Sponsor Name:Odense University Hospital | |||||||||||||
| Full Title: A designed Patient-centered Intervention to Improve medical Adherence in Topical Treatment of psoriasis - A Study protocol | |||||||||||||
| Medical condition: Psoriasis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-001556-67 | Sponsor Protocol Number: derhill2017/1 | Start Date*: 2017-05-17 | |||||||||||
| Sponsor Name:UZ Brussel | |||||||||||||
| Full Title: The effect of emollients on pruritus in psoriasis | |||||||||||||
| Medical condition: Psoriasis is traditionally considered a non-itchy skin disease. It seems that itch is an underestimated, and therefore undertreated aspect of psoriasis. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-002640-25 | Sponsor Protocol Number: RR12/10234 | Start Date*: 2013-02-07 | ||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:University of Leeds/Leeds Teaching Hospitals NHS Trust | ||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: A prospective, single-centre, feasibility study evaluating the prevalence of diagnostic clinical imaging features of subclinical enthesitis in patients with moderate to severe plaque psoriasis and ... | ||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Psoriatic disease (psoriasis and psoriatic arthritis). | ||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2016-001568-12 | Sponsor Protocol Number: 16-02/CalciBet-S | Start Date*: 2016-10-18 | |||||||||||||||||||||
| Sponsor Name:Dermapharm AG | |||||||||||||||||||||||
| Full Title: A multi-centre, randomised, double-blind, parallel-group phase III study to investigate the efficacy, safety, and tolerability of a generic calcipotriol-betamethasone ointment formulation compared ... | |||||||||||||||||||||||
| Medical condition: chronic stable plaque psoriasis | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: BG (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: 2008-005518-29 | Sponsor Protocol Number: 08F/BET01 | Start Date*: 2008-12-01 | |||||||||||
| Sponsor Name:Laboratoires GENEVRIER | |||||||||||||
| Full Title: An exploratory, open-label, intra-individual,active- controlled study comparing the efficacy and safety of Betesil versus Daivobet for the treatment of chronic plaque psoriasis | |||||||||||||
| Medical condition: Chronic plaque psoriasis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-004721-41 | Sponsor Protocol Number: CHUBX 2008/08 | Start Date*: 2008-10-07 | |||||||||||
| Sponsor Name:CHU de Bordeaux | |||||||||||||
| Full Title: Profil des populations leucocytaires chez les patients atteints de psoriasis répondeurs et non répondeurs au traitement par efaluzimab (anti-CD11A) : étude systémique et cutanée | |||||||||||||
| Medical condition: patients atteints de psoriasis modérés à sévère | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-000710-53 | Sponsor Protocol Number: RD.06.SPR.18131 | Start Date*: 2014-12-19 | |||||||||||
| Sponsor Name:GALDERMA R&D, LLC | |||||||||||||
| Full Title: A multicenter open label uncontrolled study of the long term safety and efficacy of calcitriol 3 mcg/g ointment applied twice daily for 26 weeks in pediatric subjects (2 to 16 years and 11 months o... | |||||||||||||
| Medical condition: Psoriasis | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) IT (Completed) BE (Completed) HU (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-007678-43 | Sponsor Protocol Number: P070602 | Start Date*: 2008-04-04 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: Evaluation de l'efficacité et de la tolérance de deux stratégies de prescription du Méthotrexate dans le traitement du psoriasis | |||||||||||||
| Medical condition: Psoriasis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-002738-39 | Sponsor Protocol Number: 04-7-011 | Start Date*: 2006-09-22 | |||||||||||
| Sponsor Name:Astelleas Pharma US, Inc. | |||||||||||||
| Full Title: A Phase 1 Open-Label Study of the Pharmacokinetics of Tacrolimus Cream B 0.1% after Twice Daily Topical Administration in Adolescents (≥ 12 to ≤ 17 Years of Age ) with Psoriasis | |||||||||||||
| Medical condition: Determination of pharmacokinetics and safety of tacrolimus in adolescents with plaque psoriasis | |||||||||||||
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| Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: LV (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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