- Trials with a EudraCT protocol (1,923)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,923 result(s) found for: Skin Diseases AND Skin Disease.
Displaying page 40 of 97.
| EudraCT Number: 2017-002581-51 | Sponsor Protocol Number: AK002-006 | Start Date*: 2018-01-10 | |||||||||||
| Sponsor Name:Allakos Inc. | |||||||||||||
| Full Title: An Open-Label, Pilot Study to Assess the Efficacy and Safety Of AK002 (Siglec-8) in Patients with Antihistamine-Resistant Chronic Urticaria | |||||||||||||
| Medical condition: Patients with different types of chronic urticaria resistant to standard dose antihistamines | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-005092-14 | Sponsor Protocol Number: GT-24 | Start Date*: 2013-03-12 | |||||||||||
| Sponsor Name:ALK-Abelló S.A. | |||||||||||||
| Full Title: Molecular and Cellular Mechanism in the course of Immunotherapy with a Phleum pratense oral lyophilisate | |||||||||||||
| Medical condition: Treatment of grass pollen induced rhinitis and conjunctivitis in adult patients with clinically relevant symptoms and diagnosed witha positive skin-prick test and / or specific IgE test to grass po... | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-004669-16 | Sponsor Protocol Number: C2501004 | Start Date*: 2019-09-23 | |||||||||||
| Sponsor Name:Pfizer Inc | |||||||||||||
| Full Title: A PHASE 2, RANDOMIZED, DOUBLE BLIND, PLACEBO-CONTROLLED, STUDY TO EVALUATE THE SAFETY AND EFFICACY OF PF-06826647 IN PARTICIPANTS 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: PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-001368-40 | Sponsor Protocol Number: M-41008-41 | Start Date*: 2017-09-13 | |||||||||||
| Sponsor Name:Almirall S.A. | |||||||||||||
| Full Title: Open clinical study to assess long-term efficacy and safety of dimethyl fumarate in adults with moderate to severe chronic plaque psoriasis in real practice (DIMESKIN 1 Trial) | |||||||||||||
| Medical condition: Moderate-severe chronic plaque psoriasis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-005388-30 | Sponsor Protocol Number: T525-STD-043 | Start Date*: 2022-11-21 | |||||||||||
| Sponsor Name:Inmunotek, S.L. | |||||||||||||
| Full Title: Quercus ilex and Quercus robur allergenic extracts. Determination of the in vivo allergenic potency in histamine equivalent units (HEP). | |||||||||||||
| Medical condition: Allergy to Quercus ilex and Quercus robur pollen | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-023757-11 | Sponsor Protocol Number: myDC/pDCinstageIIImelanoma | Start Date*: 2014-11-06 |
| Sponsor Name:Radboud University Nijmegen Medical Centre | ||
| Full Title: Myeloid and plasmacytoid blood dendritic cells for immunotherapy of stage III melanoma patients scheduled for radical lymph node dissection | ||
| Medical condition: melanoma patients with regional lymph node metastases (stage III) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-002255-42 | Sponsor Protocol Number: MK-3222-010 | Start Date*: 2013-01-10 | |||||||||||
| Sponsor Name:Sun Pharma Global FZE | |||||||||||||
| Full Title: A 64-Week, Phase 3, Randomized, Placebo-Controlled, Parallel Design Study to Evaluate the Efficacy and Safety/Tolerability of Subcutaneous Tildrakizumab (SCH 900222/MK-3222), Followed by an Optiona... | |||||||||||||
| Medical condition: Moderate-to-Severe Chronic Plaque Psoriasis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-000284-48 | Sponsor Protocol Number: EDP1815-208 | Start Date*: 2022-06-06 | |||||||||||
| Sponsor Name:EVELO Biosciences Inc | |||||||||||||
| Full Title: A Long-Term Extension Trial in participants with Atopic Dermatitis who participated in previous Phase 2 and 3 EDP1815 trials | |||||||||||||
| Medical condition: Mild, moderate, and severe atopic dermatitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-006885-19 | Sponsor Protocol Number: ARQ-151-313 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Arcutis Biotherapeutics, Inc. | |||||||||||||
| Full Title: A Phase 3, Multicenter, Open-Label Extension Study of the Long-Term Safety of ARQ-151 Cream 0.15% and ARQ-151 Cream 0.05% in Subjects with Atopic Dermatitis | |||||||||||||
| Medical condition: Atopic Dermatitis | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-003567-22 | Sponsor Protocol Number: Zincox12 | Start Date*: 2012-12-05 | |||||||||||
| Sponsor Name:A.O. UNIVERSITARIA INTEGRATA DI VERONA | |||||||||||||
| Full Title: Efficacy of topical application of zinc oxide ointment compared with zinc oxide paste and tocoferol, for treating diaper dermatitis in infant: a randomized, controlled, triple blind study | |||||||||||||
| Medical condition: Diaper dermatitis | |||||||||||||
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| Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-004750-39 | Sponsor Protocol Number: LEOSIC | Start Date*: 2022-07-08 | |||||||||||
| Sponsor Name:Herlev Gentofte Hospital - Department of Dermatology and Allergy | |||||||||||||
| Full Title: The role of Interleukin-1B targeted therapy for patients suffering with allergic contact dermatitis: A randomized controlled trial with Anakinra vs. Placebo. | |||||||||||||
| Medical condition: Allergic contact dermatitis. Patients with nickel allergy to be specific | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-005389-32 | Sponsor Protocol Number: T521-STD-044 | Start Date*: 2023-03-13 | |||||||||||
| Sponsor Name:Inmunotek, S.L. | |||||||||||||
| Full Title: Juniperus oxycedrus and Cupressus arizonica allergen extracts. Determination of the in vivo allergenic potency in histamine equivalent units (HEP). | |||||||||||||
| Medical condition: Allergy to Cupressaceae: Juniperus oxycedrus and Cupressus arizonica | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-005083-34 | Sponsor Protocol Number: CAPI2017NL10 | Start Date*: 2017-08-23 |
| Sponsor Name:University Medical Center Utrecht | ||
| Full Title: Conestat alfa as prophylactic treatment for idiopathic non-histaminergic acquired angioedema | ||
| Medical condition: The medical condition to be investigated is idiopathic non-histaminergic angioedema (InH-AAE). This disease is characterized by recurrent episodes with swelling of the subcutis and mucous membranes... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-001353-16 | Sponsor Protocol Number: BAY63-2521/16277 | Start Date*: 2015-04-17 | |||||||||||
| Sponsor Name:Bayer AG | |||||||||||||
| Full Title: A Randomised, Double-Blind, Placebo-Controlled Phase II Study to Investigate the Efficacy and Safety of Riociguat in Patients With Diffuse Cutaneous Systemic Sclerosis (dcSSc) | |||||||||||||
| Medical condition: diffuse cutaneous systemic sclerosis (dcSSc) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) DE (Completed) NL (Completed) BE (Completed) ES (Completed) CZ (Completed) HU (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-004705-26 | Sponsor Protocol Number: LPS15497 | Start Date*: 2020-03-24 | |||||||||||
| Sponsor Name:Sanofi Aventis Groupe | |||||||||||||
| Full Title: A randomized double blind placebo controlled study evaluating the effect of dupilumab on sleep in adult patients with moderate to severe atopic dermatitis | |||||||||||||
| Medical condition: Atopic dermatitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) FR (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-002513-36 | Sponsor Protocol Number: ASP-1929-301 | Start Date*: 2019-08-16 | |||||||||||
| Sponsor Name:Rakuten Aspyrian, Inc. | |||||||||||||
| Full Title: A Phase 3, Randomized, Double-Arm, Open-Label, Controlled Trial of ASP-1929 Photoimmunotherapy Versus Physician’s Choice Standard of Care for the Treatment of Locoregional, Recurrent Head and Neck ... | |||||||||||||
| Medical condition: Locoregional, recurrent head and neck squamous cell carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) GR (Completed) BE (Completed) ES (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-001136-21 | Sponsor Protocol Number: B7451013 | Start Date*: 2018-10-22 | |||||||||||
| Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, NY 10017 | |||||||||||||
| Full Title: A Phase 3 Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multi-Center Study to Evaluate the Efficacy and Safety of PF-04965842 Monotherapy in Subjects Aged 12 Years and Older, with M... | |||||||||||||
| Medical condition: Moderate to severe atopic dermatitis | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BG (Completed) HU (Completed) CZ (Completed) GB (Completed) DE (Completed) PL (Completed) LV (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-005450-45 | Sponsor Protocol Number: P04684 | Start Date*: 2006-08-30 | |||||||||||
| Sponsor Name:Schering-Plough Research Institute | |||||||||||||
| Full Title: Double-Blind, Randomized, Placebo-Controlled, Parallel-Group, Multicenter/ Multinational, Efficacy and Safety Study of Desloratadine 5 mg in the Treatment of Subjects With Allergic Rhinitis Who Mee... | |||||||||||||
| Medical condition: Persistent Allergic Rhinitis (Allergic Rhinitis) | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) PT (Completed) ES (Completed) DE (Completed) HU (Completed) SE (Completed) GR (Completed) DK (Completed) IT (Completed) BE (Completed) NL (Completed) Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-003200-39 | Sponsor Protocol Number: 13/0077 | Start Date*: 2014-04-01 | ||||||||||||||||||||||||||
| Sponsor Name:University College London | ||||||||||||||||||||||||||||
| Full Title: A phase II, single centre, randomised, placebo-controlled, 3-part trial to assess the safety, tolerability and efficacy of Zibotentan in patients with renal disease secondary to scleroderma | ||||||||||||||||||||||||||||
| Medical condition: Renal complications of systemic sclerosis (scleroderma renal crisis and chronic kidney disease). | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2017-001765-25 | Sponsor Protocol Number: CASM981CUS09 | Start Date*: 2017-09-28 |
| Sponsor Name:Novartis | ||
| Full Title: An Investigation of the Safety and Efficacy of Elidel® 1% Cream in Atopic Disease Modification, Assessed in a 3-year Randomized Doubleblind Vehicle Controlled Phase to Evaluate Effects on Atopic De... | ||
| Medical condition: Atopic Dermatitis | ||
| Disease: | ||
| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
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