- Trials with a EudraCT protocol (244)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18)
244 result(s) found for: Rhinoconjunctivitis.
Displaying page 1 of 13.
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: 2008-003864-20 | Sponsor Protocol Number: P05234 | Start Date*: 2009-04-14 | |||||||||||
Sponsor Name:Schering Plough Research Institute, a Division of Schering Corporation | |||||||||||||
Full Title: A Multicenter, Double-Blind, Randomized, Placebo-Controlled, Parallel-Group Study Evaluating the Efficacy and Long-Term Safety of Ragweed (Ambrosia artemisiifolia) Sublingual Tablet (SCH 39641) in ... | |||||||||||||
Medical condition: Rhinoconjunctivitis due to ragweed allergy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000031-59 | Sponsor Protocol Number: TT-02 | Start Date*: 2012-09-12 | |||||||||||
Sponsor Name:ALK-Abelló A/S | |||||||||||||
Full Title: A dose-response evaluation of ALK tree AIT | |||||||||||||
Medical condition: Subjects with a documented clinically relevant history of moderate to severe birch pollen induced allergic rhinoconjunctivitis (with or without asthma) with symptoms despite having received symptom... | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) FI (Completed) NO (Completed) SE (Completed) NL (Completed) PL (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000455-12 | Sponsor Protocol Number: SU-G-01 | Start Date*: 2021-03-05 | |||||||||||
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 5-grass mix SLIT-drops in adults with grass pollen-induced rhinoconjunctivitis | |||||||||||||
Medical condition: Grass pollen-induced allergic rhinoconjunctivitis for two years or more with or without asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) LT (Completed) LV (Completed) CZ (Completed) PL (Completed) FR (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: 2011-000120-15 | Sponsor Protocol Number: AV-G-02 | Start Date*: 2011-11-08 | |||||||||||
Sponsor Name:ALK-Abelló A/S | |||||||||||||
Full Title: AVANZ Phleum pratense maintenance dose | |||||||||||||
Medical condition: Grass pollen induced allergic rhinoconjunctivitis with or without asthma. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006009-26 | Sponsor Protocol Number: GT-18 | Start Date*: 2008-06-06 | |||||||||||
Sponsor Name:ALK-Abelló A/S | |||||||||||||
Full Title: A Phase III trial assessing the pharmacodynamic efficacy and the tolerability of Grazax® treatment initiated in the grass pollen season in subjects with seasonal grass pollen induced rhinoconjuncti... | |||||||||||||
Medical condition: Grass pollen induced rhinoconjunctivitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003861-17 | Sponsor Protocol Number: AB0803 | Start Date*: 2008-08-18 | |||||||||||
Sponsor Name:Artu Biologicals Europe B.V. | |||||||||||||
Full Title: A double-blind, randomised, placebo controlled, phase I/IIa dose escalation study to investigate the safety and tolerability of Oralgen Birch Pollen immunotherapy in patients with allergic rhinocon... | |||||||||||||
Medical condition: Allergic rhinoconjunctivitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002477-31 | Sponsor Protocol Number: AB0602/1 | Start Date*: 2007-05-23 | |||||||||||
Sponsor Name:Artu Biologicals Europe B.V. | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, multi-centre, multi-national Phase II / III follow-up study to assess long-term efficacy and safety of three different dose regimens of Oralgen® Gras... | |||||||||||||
Medical condition: Allergic rhinoconjunctivitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) LT (Completed) HU (Completed) DE (Completed) CZ (Completed) SK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003065-14 | Sponsor Protocol Number: 6078-PG-PSC-141 | Start Date*: 2007-02-26 | |||||||||||
Sponsor Name:LETI Pharma GmbH | |||||||||||||
Full Title: Investigation of a preseasonal rush treatment scheme with Depigoid® Grass Mix as an add-on therapy in patients with allergic rhinitis and/or rhinoconjunctivitis sensitized to grass pollen | |||||||||||||
Medical condition: Intermittent rhinitis and/or rhinoconjunctivitis with or without asthma bronchial caused by clinical relevant sensitisation against grass pollen. | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003415-46 | Sponsor Protocol Number: GT-12 | Start Date*: 2006-11-10 |
Sponsor Name:ALK-Abello, Group Clinical Development | ||
Full Title: A phase III trial investigating the efficacy and safety of Grazax in children aged 5-16 years with grass pollen induced rhinoconjunctivitis with or without asthma | ||
Medical condition: IgE Mediated allergy (hay fever, rhinoconjunctivitis) to grass pollen (Timothy grass, Phleum pratense) with or without asthma | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-004583-30 | Sponsor Protocol Number: BIA-DPT-P2-001 | Start Date*: 2012-01-16 |
Sponsor Name:BIAL Industrial Farmaceutica | ||
Full Title: A MULTICENTER, PHASE II, RANDOMISED, DOUBLE?BLIND, PLACEBO CONTROLED CLINICAL TRIAL OF THE SUBCUTANEOUS IMMUNOTHERAPY IN DIFFERENT DOSES WITH PARALLEL GROUPS IN SUBJECTS WITH ALLERGIC RHINOCONJUNCT... | ||
Medical condition: Allergic rhinoconjunctivitis with or without associated asthma. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-005868-10 | Sponsor Protocol Number: 6043-PG-PSC-153 | Start Date*: 2007-07-24 | |||||||||||
Sponsor Name:Laboratorios LETI S.L. | |||||||||||||
Full Title: Ensayo clínico, multicéntrico, aleatorizado, doble ciego controlado con placebo, de inmunoterapia subcutánea con extracto despigmentado y polimerizado de polen de Phleum pratense en pacientes con h... | |||||||||||||
Medical condition: Rinoconjuntivitis moderada-severa (con o sin asma episódico) inducida por hipersensibilidad frente al polen de gramíneas. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004341-27 | Sponsor Protocol Number: MK-3641-008 | Start Date*: 2016-01-05 |
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | ||
Full Title: A Phase III, Randomized, Placebo-Controlled Clinical Trial to Study the Efficacy and Safety of MK-3641, a Ragweed (Ambrosia artemisiifolia) Sublingual Immunotherapy Tablet, in Children With a Histo... | ||
Medical condition: Rhinoconjunctivitis due to ragweed allergy | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: HU (Completed) HR (Completed) Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2015-004821-15 | Sponsor Protocol Number: TT-04 | Start Date*: 2016-03-18 | |||||||||||
Sponsor Name:ALK Abello A/S | |||||||||||||
Full Title: Efficacy and safety of the SQ tree SLIT-tablet in subjects with moderate to severe allergic rhinitis and/or conjunctivitis induced by pollen from the birch group | |||||||||||||
Medical condition: Allergic Rhinoconjunctivitis induced by birch pollen | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) SE (Completed) CZ (Completed) FI (Completed) DE (Completed) PL (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004214-96 | Sponsor Protocol Number: MEIN/15/Bil-PSR/002 | Start Date*: 2017-02-02 | |||||||||||
Sponsor Name:MENARINI INTERNATIONAL OPERATIONS LUXEMBOURG SA | |||||||||||||
Full Title: Bilastine and inflammation: an explorative study in subjects affected by Parietaria J.-induced Rhinoconjunctivitis – The Bi-FLO study | |||||||||||||
Medical condition: Rhinoconjunctivitis induced by Parietaria J. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004639-39 | Sponsor Protocol Number: CYT003-QbG10 09 | Start Date*: 2008-10-03 | |||||||||||
Sponsor Name:Cytos Biotechnology AG | |||||||||||||
Full Title: Double-blind, Placebo-controlled Dose-finding Study with CYT003-QbG10 in Adult Patients with Rhinoconjunctivitis due to House Dust Mite Allergy. | |||||||||||||
Medical condition: Adult patients with perennial allergic rhinoconjunctivitis due to house dust mite | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) DE (Completed) LV (Completed) LT (Completed) GR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003593-18 | Sponsor Protocol Number: GT-19 | Start Date*: 2008-09-04 | |||||||||||
Sponsor Name:ALK-Abelló A/S | |||||||||||||
Full Title: A Phase III trial evaluating the tolerability of Grazax treatment in combination with antihistamine in subjects with seasonal grass pollen induced rhinoconjunctivitis | |||||||||||||
Medical condition: Grass pollen induced rhinoconjunctivitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001459-22 | Sponsor Protocol Number: BIA-PAR-DEPOT | Start Date*: 2015-02-20 |
Sponsor Name:Bial Industrial Farmacéutica S.A. | ||
Full Title: OPEN CLINICAL TRIAL, MULTICENTER, WITH SUBCUTANEOUS IMMUNOTHERAPY IN DEPOT PRESENTATION, IN PATIENTS WITH ALLERGY RHINOCONJUNCTIVITIS SENSITIZED TO PARIETARIA JUDAICA | ||
Medical condition: PATIENTS WITH RHINOCONJUNCTIVITIS SENSITISED TO PARIETARIA JUDAICA | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-002781-31 | Sponsor Protocol Number: PQBirch301 | Start Date*: 2017-02-16 | |||||||||||
Sponsor Name:Allergy Therapeutics (UK) Ltd | |||||||||||||
Full Title: A multi-centre, double-blind, randomised, placebo-controlled, parallel-group study to evaluate the efficacy and safety of Birch Modified Allergen Tyrosine adsorbed + MPL in the prevention of season... | |||||||||||||
Medical condition: Seasonal allergic rhinoconjunctivitis due to birch pollen | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) SE (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
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