- Trials with a EudraCT protocol (34)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
34 result(s) found for: allergopharma.
Displaying page 1 of 2.
EudraCT Number: 2006-005304-14 | Sponsor Protocol Number: AL0205PR | Start Date*: 2007-01-09 | |||||||||||
Sponsor Name:Allergopharma Joachim Ganzer KG | |||||||||||||
Full Title: Design of optimally-diagnostic skin test solutions for diagnosis of sensitisation to a 6-grass pollen mixture, house dust mite (Dermatophagoides pteronyssinus), birch pollen and mugwort pollen and ... | |||||||||||||
Medical condition: Sensitisation to one or more allergens of 6-grass pollen mixture (Holcus lanatus, Dactylis glomerata, Lolium perenne, Phleum pratense, Poa pratensis, Festuca elatior), house dust mite (Dermatophago... | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-007096-32 | Sponsor Protocol Number: PREV1234 | Start Date*: 2009-01-07 |
Sponsor Name:Medizinische Universität Wien, Univ. Kinderklinik | ||
Full Title: Prevention od new sensitization by sublingual immunotherapy in children 2-4 years of age with allergic mono-sensitization | ||
Medical condition: Children (2-4years of age) from atopy prone families with an allergic sensitization as defined by positive skin prick test or positive allergen-specific IgE to grass pollen or house dust mite aller... | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-001914-41 | Sponsor Protocol Number: AL1201AV | Start Date*: 2012-10-19 | ||||||||||||||||
Sponsor Name:Allergopharma Joachim Ganzer KG | ||||||||||||||||||
Full Title: Open label phase II multicentre clinical trial to evaluate safety during shortened uptitration of an allergoid grass pollen preparation in adult patients with IgE mediated allergic rhinitis / rhino... | ||||||||||||||||||
Medical condition: ICD classificationcode: J 45.0 and J30.1 Patients with IgE mediated allergic rhinitis / rhinoconjunctivitis with or without controlled bronchial asthma | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-003095-12 | Sponsor Protocol Number: AL1303AV | Start Date*: 2014-03-19 | ||||||||||||||||
Sponsor Name:Allergopharma GmbH & Co. KG | ||||||||||||||||||
Full Title: Double-blind phase IV multicentre clinical trial to evaluate and compare specific and non specific effects of SCIT by use of an Environmental Challenge Chamber after treatment with Allergovit® gras... | ||||||||||||||||||
Medical condition: Patients suffering from seasonal allergic rhinoconjunctivitis with or without controlled asthma during the birch and grass pollen season | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-005452-16 | Sponsor Protocol Number: AL0705AV | Start Date*: 2008-03-10 |
Sponsor Name:Allergopharma Joachim Ganzer KG an afilliate of Merck KGaA, Darmstadt | ||
Full Title: A multicentre randomised placebo-controlled, double-blind clinical trial for eval¬ua¬tion of safety and efficacy of pre-seasonal specific immunotherapy with a hypoallergenic extract of a 6 grass an... | ||
Medical condition: IgE-mediated allergic diseases including symptoms of allergic rhinoconjunctivitis, controlled allergic bronchial asthma, triggered by grass/rye pollen allergens | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: PT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2020-004328-41 | Sponsor Protocol Number: AL0001nh | Start Date*: 2021-05-04 | ||||||||||||||||
Sponsor Name:Allergopharma GmbH & Co. KG | ||||||||||||||||||
Full Title: A multicentre, randomized, open label clinical trial for the safety evaluation of a short dose escalation scheme using one strength for allergen immunotherapy with an aluminium-hydroxide adsorbed n... | ||||||||||||||||||
Medical condition: moderate to severe allergic rhinitis or rhinoconjunctivitis with or without asthma | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-002317-34 | Sponsor Protocol Number: AL2101av | Start Date*: 2021-12-20 | ||||||||||||||||
Sponsor Name:Allergopharma GmbH & Co. KG | ||||||||||||||||||
Full Title: A multicenter, randomized, open label clinical trial for safety evaluation of an allergen immunotherapy with an accelerated dose escalation schedule using one strength of an aluminium hydroxide ads... | ||||||||||||||||||
Medical condition: moderate to severe seasonal allergic rhinitis or rhinoconjunctivitis with or w/o asthma caused by birch pollen allergens | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-000597-29 | Sponsor Protocol Number: 2017-02-CHRMT | Start Date*: 2021-06-02 |
Sponsor Name:Centre Hospitalier Régional Metz-Thionville | ||
Full Title: Interest of Nasal Provocation Tests for Diagnosis of House Mites Allergic Rhinitis | ||
Medical condition: mite allergenic rhinitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000548-25 | Sponsor Protocol Number: AL1605av | Start Date*: 2018-06-18 | |||||||||||||||||||||||||||||||
Sponsor Name:Allergopharma GmbH & Co. KG | |||||||||||||||||||||||||||||||||
Full Title: A multicentre, randomized, open label clinical trial for safety evaluation of an accelerated high dose escalation schedule with one strength for an allergen immunotherapy with an aluminium hydroxid... | |||||||||||||||||||||||||||||||||
Medical condition: Patients with moderate to severe seasonal rhinitis or rhinoconjunctivitis with or without asthma | |||||||||||||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) ES (Completed) PL (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-002248-29 | Sponsor Protocol Number: AL1009ac | Start Date*: 2012-03-07 |
Sponsor Name:Allergopharma Joachim Ganzer KG | ||
Full Title: A multicentre randomised placebo-controlled double-blind clinical trial for evaluation of the optimal dose for safety and efficacy of specific immunotherapy with an aluminium hydroxide-adsorbed All... | ||
Medical condition: Controlled allergic bronchial asthma + rhinitis/rhinoconjunctivitis induced by house dust mite | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: PL (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-000674-58 | Sponsor Protocol Number: AL1011av | Start Date*: 2011-07-28 | ||||||||||||||||
Sponsor Name:Allergopharma Joachim Ganzer KG | ||||||||||||||||||
Full Title: Double-blind, placebo controlled study to investigate the dose response of an allergoid preparation of Phleum pratense in adult patients with IgE mediated allergic Rhinitis / Rhinoconjunctivitis wi... | ||||||||||||||||||
Medical condition: ICD classification code: J 45.0 and J 30.1 | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
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: 2012-003281-40 | Sponsor Protocol Number: 2712 | Start Date*: 2012-10-23 |
Sponsor Name:Universitätsklinikum Freiburg | ||
Full Title: Efficacy of gencydo nasal spray on early nasal response after allergen exposition in patients with grass pollen allergy: a randomized, placebo controlled cross over study | ||
Medical condition: Hay fever caused by grass pollen allergy | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-003892-35 | Sponsor Protocol Number: AL 0104 av | Start Date*: 2005-04-01 |
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 disease in adults and children manifested as bronchial asthma (GINA II and III) +/-allergic rhinitis/rhinoconjunctivitis, triggered by non-eliminable house dust mite allergens. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-000188-15 | Sponsor Protocol Number: AL1402ac | Start Date*: 2017-01-09 | |||||||||||||||||||||
Sponsor Name:Allergopharma GmbH & Co. KG | |||||||||||||||||||||||
Full Title: A multicenter randomized double-blind placebo-controlled clinical trial for evaluation of efficacy and safety of specific immunotherapy with an aluminium hydroxide-adsorbed allergoid preparation o... | |||||||||||||||||||||||
Medical condition: allergic bronchial asthma and allergic rhinitis or rhinoconjunctivitis | |||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: PL (Completed) LT (Completed) DE (Completed) ES (Completed) LV (Completed) AT (Completed) HR (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-005645-31 | Sponsor Protocol Number: 205540 | Start Date*: 2016-10-14 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: A randomised, double-blind (sponsor open) placebo-controlled, parallel group, 8-week treatment study to investigate the safety, pharmacodynamics, and effect of the TLR7 agonist, GSK2245035, on the... | |||||||||||||
Medical condition: Mild allergic asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000594-24 | Sponsor Protocol Number: 12/014/TAR | Start Date*: 2012-04-19 | |||||||||||
Sponsor Name:Royal Sussex County Hospital | |||||||||||||
Full Title: An open study to investigate the effects of injection immunotherapy on allergen-specific T and B cell responses in adult patients with seasonal allergic rhinitis. | |||||||||||||
Medical condition: Allergic Rhinitis due to birch or grass pollen | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002808-18 | Sponsor Protocol Number: AL0701rP | Start Date*: 2007-10-31 | ||||||||||||||||
Sponsor Name:ALLERGOPHARMA JOACHIM GANZER KG | ||||||||||||||||||
Full Title: A double-blind placebo controlled dose-response study for evaluation of safety and efficacy of immunotherapy with a cocktail of recombinant major allergens of Timothy Grass Pollen (Phleum pratense)... | ||||||||||||||||||
Medical condition: ICD classification code: J45.0 and J30.1 | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-011504-36 | Sponsor Protocol Number: AL0906rP | Start Date*: 2010-02-02 | ||||||||||||||||
Sponsor Name:Allergopharma Joachim Ganzer KG | ||||||||||||||||||
Full Title: Randomised double blind placebo controlled pivotal study to evaluate efficacy and safety of rPhleum in adult and adolescent patients suffering from rhinoconjunctivitis +/- controlled Asthma | ||||||||||||||||||
Medical condition: ICD classification code: J45.0 and J 30.1 Rhiniconjunctivitis +/- asthma bronchiale | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) GB (Completed) PL (Completed) FR (Completed) ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-005400-28 | Sponsor Protocol Number: AL1502AV | Start Date*: 2016-06-20 | |||||||||||||||||||||||||||||||
Sponsor Name:Allergopharma GmbH & Co. KG | |||||||||||||||||||||||||||||||||
Full Title: Open label phase II multicenter clinical trial to evaluate safety during accelerated dose escalation of an allergoid birch pollen preparation in patients with IgE mediated allergic rhinitis or rhin... | |||||||||||||||||||||||||||||||||
Medical condition: Patients with seasonal rhinitis or rhinoconjunctivitis with or without controlled asthma during the birch pollen season | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
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