- Trials with a EudraCT protocol (11)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
11 result(s) found for: Antiallergic.
Displaying page 1 of 1.
EudraCT Number: 2005-000025-35 | Sponsor Protocol Number: Al0204AV | Start Date*: 2005-04-05 |
Sponsor Name:Allergopharma Joachim Ganzer KG | ||
Full Title: A multicentre randomised placebo-controlled double-blind clinical trial for evaluation of safety and efficacy of specific immunotherapy with an aluminium hydroxide-adsorbed allergoid preparation of... | ||
Medical condition: IgE-mediated allergic diseases including allergic rhinitis/rhinoconjunctivitis, allergic bronchial asthma (GINA I and II) triggered by birch pollen allergens | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) FI (Completed) SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-000934-11 | Sponsor Protocol Number: Al0106ac | Start Date*: 2006-08-11 |
Sponsor Name:Alllergopharma Joachim Ganzer KG | ||
Full Title: A multicentre randomised placebo-controlled double-blind clinical trial for evaluation of safety and efficacacy of a specific immunotherapy with an aluminium hydroxide-adsorbed allergoid preparatio... | ||
Medical condition: IgE-mediated allergic disease in adults manifested as rhinitis/ rhinoconjunctivitis and/or allergic asthma bronchiale (GINA I and II) triggered by non eliminable house dust mite allergens. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-002835-27 | Sponsor Protocol Number: DRP-05-12 | Start Date*: 2012-09-07 |
Sponsor Name:Dr. Ritsert Pharma | ||
Full Title: Double-blind, randomized clinical study to determine the efficacy of Anestherit® 10% on histamine-induced pruritus and UVB-light induced slight sunburn in healthy subjects. | ||
Medical condition: Histamine-induced pruritus UVB-light-induced slight sunburn | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-002350-63 | Sponsor Protocol Number: SL300/2004/002/D | Start Date*: 2004-11-19 |
Sponsor Name:Stallergenes GmbH & Co.KG | ||
Full Title: Efficacy and Safety of Sublingual Immunotherapy with Ultra-Rush Titration in Children with Allergic Rhinoconjunctivitis to Tree Pollen, a Multicentre DBPC Trial | ||
Medical condition: Allergic rhinitis against birch pollen | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-004522-10 | Sponsor Protocol Number: Lais-Amb-11 | Start Date*: 2012-05-06 | |||||||||||
Sponsor Name:LOFARMA | |||||||||||||
Full Title: Study on the efficacy and safety of three different doses of Lais Ambrosia tablets in patients with allergic rhinoconjunctivitis to pollen of Ambrosia | |||||||||||||
Medical condition: rhinoconjunctivitis allergic to ragweed pollen | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001029-84 | Sponsor Protocol Number: AL0702rB | Start Date*: 2007-08-30 | ||||||||||||||||
Sponsor Name:Allergopharma Joachim Ganzer KG | ||||||||||||||||||
Full Title: A multicentre randomised, placebo-controlled, double-blind pivotal clinical trial for the evaluation of safety and efficacy of specific of immunotherapy with an aluminium hydroxide-adsorbed hypoall... | ||||||||||||||||||
Medical condition: ICD classification code: J45.0 and J30.1 | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) SE (Completed) FI (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-000083-27 | Sponsor Protocol Number: GT-08 | Start Date*: 2004-09-19 |
Sponsor Name:ALK-Abelló A/S | ||
Full Title: A randomised, parallel-group, double-blind, placebo-controlled Phase III trial assessing the efficacy and safety of ALK Grass Tablet Phleum pratense in subjects with seasonal grass pollen induced r... | ||
Medical condition: Rhinoconjunctivitis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) IT (Completed) ES (Completed) AT (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-004916-79 | Sponsor Protocol Number: SMART_10 | Start Date*: 2013-02-26 | |||||||||||
Sponsor Name:Lofarma S.p.A. | |||||||||||||
Full Title: Efficacy and Safety of sublingual immunotherapy with Allergoid LAIS® Grass tablets for patients with grass pollen-induced allergic rhinoconjunctivitis, a phase III study | |||||||||||||
Medical condition: Patients suffering from allergic rhinoconjunctivitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002129-43 | Sponsor Protocol Number: SMART_7 | Start Date*: 2013-12-09 | |||||||||||
Sponsor Name:Lofarma S.p.A. | |||||||||||||
Full Title: Efficacy and Safety of sublingual immunotherapy with Allergoid LAIS®Birch-Alder tablets for patients with tree pollen-induced allergic rhinoconjunctivitis A Phase III study | |||||||||||||
Medical condition: Patients suffering from allergic rhinoconjunctivitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004185-14 | Sponsor Protocol Number: CDPG103ADE01 | Start Date*: 2012-02-29 | |||||||||||||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||||||||||||
Full Title: A multicenter, randomized, double-blind, placebo-controlled, parallel-group study to evaluate the efficacy and safety of intraseasonal specific short-term immunotherapy with depigmented glutaraldeh... | |||||||||||||||||||||||
Medical condition: Allergic rhinitis and/or rhinoconjunctivitis with or without intermittent asthma. | |||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-018562-23 | Sponsor Protocol Number: 6078-PG-PSC-169 | Start Date*: 2010-09-15 | |||||||||||||||||||||
Sponsor Name:LETI Pharma GmbH | |||||||||||||||||||||||
Full Title: A Randomised, Double-Blind, Parallel Group, Multicentre Study to Assess the Efficacy and Safety of Four Concentrations of Depigoid® Phleum in Patients with Allergic Rhinitis and/or Rhinoconjunctivi... | |||||||||||||||||||||||
Medical condition: Allergic rhinitis and/or allergic rhinoconjunctivitis with or without intermittent asthma. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: CZ (Prematurely Ended) BG (Ongoing) HU (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
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