- Trials with a EudraCT protocol (198)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
198 result(s) found for: Histamine.
Displaying page 7 of 10.
EudraCT Number: 2019-003036-23 | Sponsor Protocol Number: 19SM5101 | Start Date*: 2019-12-02 | |||||||||||||||||||||||||||||||
Sponsor Name:Imperial College London | |||||||||||||||||||||||||||||||||
Full Title: Mechanisms of adverse effects of long-acting beta-agonists in asthma | |||||||||||||||||||||||||||||||||
Medical condition: Asthma | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003066-34 | Sponsor Protocol Number: 101-PG-PSC-150 | Start Date*: 2007-01-23 | |||||||||||
Sponsor Name:LETI Pharma GmbH | |||||||||||||
Full Title: A randomized, double blinded, placebo controlled multicenter study for the efficacy and safety of Depigoid® House dust mites (HDM) in patients suf-fering from moderate to severe atopic eczema. | |||||||||||||
Medical condition: Moderate to severe atopic eczema with or without rhinitis and/or rhinoconjunctivitis caused by clinical relevant IgE-mediated sensitization against House dust mites (HDM) leading to aggravation of ... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003063-34 | Sponsor Protocol Number: GSDL_DE_17 | Start Date*: 2017-12-11 | |||||||||||
Sponsor Name:Lofarma S.p.A. | |||||||||||||
Full Title: A double-blind, placebo-controlled dose-escalation study of carbamylated monomeric tree pollen drops in patients with a history of allergic rhinoconjunctivitis. | |||||||||||||
Medical condition: Treatment of tree pollen-induced allergic rhinoconjunctivitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-005079-21 | Sponsor Protocol Number: LOTAB_2b_HDM | Start Date*: 2018-08-23 | |||||||||||
Sponsor Name:Lofarma S.p.A. | |||||||||||||
Full Title: A Prospective, Multicenter, Double-Blind, Placebo-Controlled, Dose-Finding Phase-II Study for the Efficacy and Safety of LAIS® House Dust Mites Sublingual Tablets in Patients with Mite-Induced Alle... | |||||||||||||
Medical condition: Patients Suffering from Mite-Induced Allergic Rhino-Conjunctivitis Without or With Controlled Asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005084-32 | Sponsor Protocol Number: D6230C00001 | Start Date*: 2015-06-05 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, parallel group, multi-centre Phase IIa study in asthma patients comparing the efficacy and safety of once daily inhaled Interferon beta-1a to placebo... | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002047-18 | Sponsor Protocol Number: SM/0044 | Start Date*: 2015-01-14 | |||||||||||
Sponsor Name:HAL Allergy B.V. | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled study to determine tolerability and safety of different dosages of SUBLIVAC FIX Mite mixture in patients with allergic rhinitis / rhinoconjunctivitis ... | |||||||||||||
Medical condition: Patients, 18-60 years of age, suffering from house dust mites-induced persistent allergic rhinitis/rhinoconjunctivitis with or without concomitant at least partly controlled asthma. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-002252-36 | Sponsor Protocol Number: T502-SIT-045 | Start Date*: 2021-10-27 | |||||||||||
Sponsor Name:Inmunotek S.L. | |||||||||||||
Full Title: A prospective, randomized, double-blind placebo-controlled multicentre study with 10 000 mTU/mL mannan-conjugated birch pollen allergoids administered subcutaneously to patients with birch pollen-i... | |||||||||||||
Medical condition: Treatment of birch pollen-induced allergic rhinitis or rhinoconjunctivitis. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001291-38 | Sponsor Protocol Number: Salsa | Start Date*: 2018-08-08 | |||||||||||
Sponsor Name:Radboud University Medical Center | |||||||||||||
Full Title: In vivo efficacy of Salbutamol Sandoz versus salbutamol Ventolin GSK in children with asthma | |||||||||||||
Medical condition: Asthma in children | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002522-23 | Sponsor Protocol Number: T502-SIT-020 | Start Date*: 2019-08-21 | |||||||||||
Sponsor Name:Inmunotek S.L. | |||||||||||||
Full Title: A prospective, randomized, double-blind placebo-controlled dose-finding study of different regimens of mannan-conjugated allergoids of birch pollen allergens administered subcutaneously to patients... | |||||||||||||
Medical condition: Treatment of birch pollen-induced allergic rhinitis or rhinoconjunctivitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-006681-21 | Sponsor Protocol Number: FVGEXACT@home2021 | Start Date*: 2022-11-17 | |||||||||||
Sponsor Name:Franciscus Gasthuis & Vlietland | |||||||||||||
Full Title: Expertise Asthma COPD Program with Digital Support | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000353-20 | Sponsor Protocol Number: VR475/3/001 | Start Date*: 2015-10-01 | |||||||||||
Sponsor Name:Vectura Limited | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, parallel group study to evaluate the efficacy and safety of two doses of nebulised budesonide delivered by the VR475 Inhalation System, with an open-... | |||||||||||||
Medical condition: Uncontrolled Asthma | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) BG (Completed) PL (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000571-85 | Sponsor Protocol Number: AN-EPI3333 | Start Date*: 2017-06-15 |
Sponsor Name:ANTHERA Pharmaceuticals, Inc. | ||
Full Title: A Phase 3, Randomized, Open-Label, Assessor-Blind, Non-Inferiority, Active-Comparator Study Evaluating the Efficacy and Safety of Liprotamase in Subjects with Cystic Fibrosis-Related Exocrine Pancr... | ||
Medical condition: Pancreatic Exocrine Insufficiency due to Cystic Fibrosis | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: HU (Prematurely Ended) ES (Prematurely Ended) PL (Prematurely Ended) GB (Prematurely Ended) LT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2011-001360-21 | Sponsor Protocol Number: CD-RI-CAT-354-1049 | Start Date*: 2011-09-07 | |||||||||||
Sponsor Name:AstraZeneca AB R&D Mölndal | |||||||||||||
Full Title: A Phase 2b, Randomized, Double-blind Study to Evaluate the Efficacy of Tralokinumab in Adults with Uncontrolled, Severe Asthma | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) CZ (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002911-33 | Sponsor Protocol Number: ABT-gpASIT011 | Start Date*: 2018-12-18 | |||||||||||
Sponsor Name:ASIT biotech S.A. | |||||||||||||
Full Title: A multicentre, international, randomised, double-blind, placebo controlled study to demonstrate the clinical efficacy and safety of subcutaneous immunotherapy with gpASIT+™ in patients with grass p... | |||||||||||||
Medical condition: Treatment of seasonal grass pollen-induced rhinoconjunctivitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) CZ (Prematurely Ended) HU (Prematurely Ended) BE (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002088-18 | Sponsor Protocol Number: H3A106104 | Start Date*: 2006-10-12 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: An open label, dose escalation study with a double blind randomised placebo controlled withdrawal to examine the effects of the histamine H3 antagonist GSK189254 in patients with narcolepsy. | |||||||||||||
Medical condition: Narcolepsy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) NL (Prematurely Ended) AT (Completed) FI (Prematurely Ended) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001251-40 | Sponsor Protocol Number: MEA115588 | Start Date*: 2012-10-16 |
Sponsor Name:GlaxoSmithKline Research and Development Limited | ||
Full Title: MEA115588 A randomised, double-blind, double-dummy, placebo-controlled, parallel-group, multi-centre study of the efficacy and safety of mepolizumab adjunctive therapy in subjects with severe uncon... | ||
Medical condition: Subjects with severe, refractory, uncontrolled asthma with elevated blood eosinphils | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) GB (Completed) DE (Completed) ES (Completed) IT (Completed) Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2018-002242-36 | Sponsor Protocol Number: GB001-2001 | Start Date*: 2018-12-06 | |||||||||||
Sponsor Name:GB001, Inc. | |||||||||||||
Full Title: A Phase 2b, randomized, double-blind, placebo-controlled, dose-ranging, multi-center study to evaluate the efficacy and safety of GB001 as maintenance therapy in adult subjects with moderate to sev... | |||||||||||||
Medical condition: Eosinophilic Asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) BE (Completed) AT (Completed) ES (Completed) GB (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-008448-26 | Sponsor Protocol Number: 603-PG-PSC-173 | Start Date*: 2009-10-20 | ||||||||||||||||
Sponsor Name:LETI Pharma GmbH | ||||||||||||||||||
Full Title: Randomized, double-blind, parallel group, multicenter study to evaluate the efficacy and safety of four doses of depigmented glutaraldehyde polymerized birch pollen allergenic extract (Depigoid® Bi... | ||||||||||||||||||
Medical condition: Allergic rhinitis and/or rhinoconjunctivitis, with or without intermittent asthma, caused by birch pollen. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) LT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-003208-37 | Sponsor Protocol Number: AL0704rP | Start Date*: 2008-01-18 | ||||||||||||||||
Sponsor Name:Allergopharma Joachim Ganzer KG | ||||||||||||||||||
Full Title: A multicentre multinational randomised, placebo-controlled, double-blind pivotal trial for the evaluation of safety and efficacy of specific immunotherapy with a cocktail of recombinant major aller... | ||||||||||||||||||
Medical condition: ICD classification code: J45.0 and J 30.1 | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-004117-33 | Sponsor Protocol Number: H3B109689 | Start Date*: 2007-12-17 | |||||||||||
Sponsor Name:GlaxoSmithKline R&D Ltd | |||||||||||||
Full Title: A single blind, placebo-controlled, randomised study in mild to moderate Alzheimer's disease patients to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of GSK239512, a selec... | |||||||||||||
Medical condition: Alzheimer's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) CZ (Completed) | |||||||||||||
Trial results: View results |
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