- Trials with a EudraCT protocol (12)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
12 result(s) found for: Pustular Palmoplantar Psoriasis.
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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: 2016-004573-40 | Sponsor Protocol Number: 1368-0015 | Start Date*: 2017-04-28 | |||||||||||
Sponsor Name:Boehringer Ingelheim AB | |||||||||||||
Full Title: Multi-center, double-blind, randomised, placebo-controlled, phase IIa study to investigate efficacy, safety, tolerability, pharmacokinetics and pharmacogenomics of multiple intravenous doses of BI ... | |||||||||||||
Medical condition: Palmoplantar Pustulosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) ES (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000189-41 | Sponsor Protocol Number: 1368-0024 | Start Date*: 2020-07-08 | |||||||||||
Sponsor Name:Boehringer Ingelheim RCV GmbH & Co KG | |||||||||||||
Full Title: An open-label, single arm, long term trial of Spesolimab treatment in patients with Palmoplantar Pustulosis (PPP) who have completed previous BI Spesolimab trials | |||||||||||||
Medical condition: Palmoplantar Pustulosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) BE (Completed) FR (Prematurely Ended) PL (Completed) CZ (Completed) GB (GB - no longer in EU/EEA) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003078-28 | Sponsor Protocol Number: 1368-0016 | Start Date*: 2019-07-01 | |||||||||||
Sponsor Name:SCS Boehringer Ingelheim Comm.V | |||||||||||||
Full Title: Multi-center, double-blind, randomised, placebo-controlled, phase IIb dose-finding study to evaluate efficacy and safety of different subcutaneous doses of BI 655130 in patients with moderate to ... | |||||||||||||
Medical condition: Palmoplantar Pustulosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) FR (Completed) CZ (Completed) PL (Completed) GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022843-39 | Sponsor Protocol Number: ATN117221 | Start Date*: 2011-04-08 | |||||||||||
Sponsor Name:GlaxoSmithKline R&D Ltd | |||||||||||||
Full Title: Efficacy of oral alitretinoin treatment in patients with palmo-plantar pustulosis (PPP) inadequately responding to standard topical treatment | |||||||||||||
Medical condition: Palmo-Plantar Pustulosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004451-20 | Sponsor Protocol Number: DER201702 | Start Date*: 2019-07-17 | |||||||||||
Sponsor Name:Rheinische Friedrich-Wilhelms-Universität Bonn | |||||||||||||
Full Title: A multicenter, open label, single-arm pilot study to evaluate the efficacy and safety of guselkumab in patients with moderate to severe palmoplantar pustulosis (PPP) | |||||||||||||
Medical condition: Adult men and women with palmoplantar pustulosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003029-31 | Sponsor Protocol Number: RIST4721-202 | Start Date*: 2022-04-27 | |||||||||||
Sponsor Name:Aristea Therapeutics Inc. | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Dose Ranging Phase 2 Study to Evaluate the Efficacy and Safety of RIST4721 in Subjects with Palmoplantar Pustulosis | |||||||||||||
Medical condition: Palmoplantar Pustulosis (PPP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) CZ (Prematurely Ended) HU (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003922-70 | Sponsor Protocol Number: TUD-PPPDD1-021 | Start Date*: 2007-11-28 | |||||||||||
Sponsor Name:Technische Universität Dresden | |||||||||||||
Full Title: Uncontrolled, open Phase IIa study to investigate efficacy and safety of efalizumab in patients with moderate to severe palmoplantar pustular psoriasis (PPP) | |||||||||||||
Medical condition: moderate to severe palmoplantar pustular psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
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: 2018-003206-58 | Sponsor Protocol Number: CNTO1959PSO3013 | Start Date*: 2019-06-29 | |||||||||||
Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
Full Title: A Phase 3b, Multicenter, Interventional, Randomized, Placebo controlled Study Investigating the Efficacy and Safety of Guselkumab for the Treatment of Palmoplantar-non-Pustular Psoriasis | |||||||||||||
Medical condition: Palmoplantar non-Pustular Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) ES (Ongoing) GB (GB - no longer in EU/EEA) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003600-23 | Sponsor Protocol Number: APRICOT | Start Date*: 2016-04-01 | |||||||||||
Sponsor Name:Guy's and St Thomas NHS Foundation Trust | |||||||||||||
Full Title: Treatment of Pustular Psoriasis with the IL-1 receptor antagonist anakinra: a randomised, placebo controlled trial and associated mechanistic studies | |||||||||||||
Medical condition: Acral Pustular Psoriasis, specifically but not limited to Palmo-Plantar Pustulosis will be the target population for therapeutic intervention with Anakinra in this study. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-006931-25 | Sponsor Protocol Number: N/A | Start Date*: 2022-03-24 | |||||||||||
Sponsor Name:Bispebjerg and Frederiksberg Hospital, University of Copenhagen | |||||||||||||
Full Title: Efficacy and safety of oral roflumilast in the treatment of palmoplantar pustulosis – a randomised controlled trial | |||||||||||||
Medical condition: Palmoplantar pustulosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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