- Trials with a EudraCT protocol (416)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
416 result(s) found for: Plaque Psoriasis.
Displaying page 1 of 21.
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: 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: 2015-003287-37 | Sponsor Protocol Number: EMR200588-002 | Start Date*: 2016-03-15 | |||||||||||
Sponsor Name:Merck KGaA | |||||||||||||
Full Title: A randomized, double-blind, confirmatory trial to evaluate the efficacy, safety and immunogenicity of MSB11022 compared with European Union-Approved Humira® in subjects with moderate to severe chro... | |||||||||||||
Medical condition: moderate to severe plaque psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) DE (Completed) GB (Completed) CZ (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003513-28 | Sponsor Protocol Number: PS0005 | Start Date*: 2015-03-27 | |||||||||||
Sponsor Name:UCB Biopharma, SPRL | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-blind, Parallel-group Study Followed by a Dose-blind Period and Open Label Follow-up to Evaluate the Efficacy and Safety of Certolizumab Pegol in Subjects... | |||||||||||||
Medical condition: Plaque Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) HU (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: 2011-002970-22 | Sponsor Protocol Number: I1F-MC-RHAZ(c) | Start Date*: 2012-05-31 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: Protocol I1F-MC-RHAZ A Multicenter Study with a Randomized, Double-Blind, Placebo-Controlled Induction Dosing Period Followed by a Randomized Maintenance Dosing Period and a Long- Term Extensio... | |||||||||||||
Medical condition: Moderate to severe chronic plaque psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) HU (Completed) PL (Completed) IT (Completed) DK (Completed) | |||||||||||||
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: 2021-004320-16 | Sponsor Protocol Number: 77242113PSO2002 | Start Date*: 2022-07-05 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Phase 2b Multicenter, Long-Term Extension, Dose-ranging Study to Evaluate the Efficacy and Safety of JNJ-77242113 for the Treatment of Moderate-to-Severe Plaque Psoriasis | |||||||||||||
Medical condition: Plaque Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Ongoing) PL (Completed) | |||||||||||||
Trial results: View results |
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: 2020-004061-39 | Sponsor Protocol Number: CNTO1959PSO4015 | Start Date*: 2021-10-22 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Phase 4, Interventional, Single-arm, Open-label Study Evaluating the Effect of Guselkumab on Cardiovascular Risk Surrogate Markers in Participants With Moderate to Severe Plaque Psoriasis | |||||||||||||
Medical condition: Plaque Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) SE (Completed) GR (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
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: 2016-000121-40 | Sponsor Protocol Number: CNTO1275PSO3013 | Start Date*: 2016-05-02 | |||||||||||
Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
Full Title: A Phase 3 Open-label Study to Assess the Efficacy, Safety, and Pharmacokinetics of Subcutaneously Administered Ustekinumab in the Treatment of Moderate to Severe Chronic Plaque Psoriasis in Pedia... | |||||||||||||
Medical condition: Moderate to Severe Chronic Plaque Psoriasis | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) HU (Completed) DE (Completed) PL (Completed) FR (Completed) NL (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001066-17 | Sponsor Protocol Number: CNTO1959PSO2001 | Start Date*: 2012-04-10 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Phase 2 Multicenter, Randomized, Placebo- and Active-Comparator-Controlled, Dose-Ranging Trial to Evaluate CNTO 1959 for the Treatment of Subjects with Moderate to Severe Plaque-type Psoriasis (X... | |||||||||||||
Medical condition: Moderate to Severe Plaque-type Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001891-31 | Sponsor Protocol Number: PS0010 | Start Date*: 2016-10-27 | |||||||||||
Sponsor Name:UCB Biopharma SPRL | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Dose Ranging Study to Evaluate the Safety, Efficacy, Pharmacokinectics, and Pharmacodynamics of Bimekizumab in Adult sub... | |||||||||||||
Medical condition: Chronic Plaque Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) CZ (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
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 |
EudraCT Number: 2011-006057-28 | Sponsor Protocol Number: CAIN457A2308 | Start Date*: 2012-06-11 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, double-blind, placebo controlled, multicenter study of subcutaneous secukinumab in prefilled syringes to demonstrate efficacy after twelve weeks of treatment, and to assess the safety... | |||||||||||||
Medical condition: Moderate to severe chronic plaque-type psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003486-14 | Sponsor Protocol Number: PS0002 | Start Date*: 2015-04-27 | |||||||||||
Sponsor Name:UCB Biopharma, SPRL | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-Blind, Parallel-group Study Followed by a Dose-blind Period and Open-label Follow-up to Evaluate the Efficacy and Safety of Certolizumab Pegol in Subjects... | |||||||||||||
Medical condition: Plaque Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) AT (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: 2016-001531-12 | Sponsor Protocol Number: LRP/LNP1955/2016/003 | Start Date*: 2016-08-16 | |||||||||||
Sponsor Name:Lupin Limited | |||||||||||||
Full Title: A Phase II, Dose Ranging, Exploratory Clinical Study to Assess the Efficacy, Pharmacodynamics, and Safety of LNP1955 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: HU (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 |
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