- Trials with a EudraCT protocol (74)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
74 result(s) found for: Dust mites.
Displaying page 1 of 4.
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: 2015-000820-27 | Sponsor Protocol Number: MM09-SIT-013 | Start Date*: 2016-02-16 | |||||||||||
Sponsor Name:Inmunotek, S.L. | |||||||||||||
Full Title: Double blind, placebo-controlled, dose finding, prospective, multicenter clinical trial for the treatment of rhinitis/rinoconjuntivitis against a mixture of Dermatophagoides pteronyssinus and Derma... | |||||||||||||
Medical condition: Mites allergy | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000870-79 | Sponsor Protocol Number: 101-PG-PSC-186 | Start Date*: 2012-02-17 | |||||||||||
Sponsor Name:Laboratorios LETI, S.L.U. | |||||||||||||
Full Title: Prospective study to evaluate the safety of a 4-month treatment with Depigoid® Dermatophagoides pteronyssinus or 50% Dermatophagoides pteronyssinus / 50% Dermatophagoides farinae (500 DPP/ml) in pa... | |||||||||||||
Medical condition: Allergic rhinitis or rhinoconjunctivitis with or without mild persistent or intermittent asthma, to Dermatophagoides pteronyssinus or Dermatophagoides pteronyssinus and Dermatophagoides farinae. | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000617-20 | Sponsor Protocol Number: SMART_2 | Start Date*: 2013-08-23 | |||||||||||
Sponsor Name:Lofarma S.p.A. | |||||||||||||
Full Title: A Dose Finding Study of the Efficacy of LAIS® Mites Sublingual tablets in patients suffering from house dust mite-induced allergic rhinoconjunctivitis A prospective, double-blind, placebo-controlle... | |||||||||||||
Medical condition: Patients suffering from allergic rhinoconjunctivitis | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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 ... | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (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. | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001454-77 | Sponsor Protocol Number: VO57.07 | Start Date*: 2007-09-12 | |||||||||||
Sponsor Name:Stallergenes S.A | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, multi-national Phase II/III study of the safety and efficacy of two doses of sublingual immunotherapy (SLIT) administered as allergen-based tablets o... | |||||||||||||
Medical condition: House dust mite allergic rhinitis | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) FR (Completed) DE (Completed) ES (Completed) NL (Completed) SK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000446-34 | Sponsor Protocol Number: MT-18 | Start Date*: 2020-07-14 | |||||||||||
Sponsor Name:ALK-Abelló A/S | |||||||||||||
Full Title: A 28-day, single-armed, open-label trial to evaluate safety of the house dust mite (HDM) sublingual allergy immunotherapy (SLIT) tablet in adolescent subjects (12-17 years of age) with HDM allergic... | |||||||||||||
Medical condition: Allergic rhinitis/rhinoconjunctivitis induced by house dust mite | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) DE (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004262-34 | Sponsor Protocol Number: MM09-SIT-023 | Start Date*: 2020-04-28 | |||||||||||||||||||||
Sponsor Name:Inmunotek, S.L. | |||||||||||||||||||||||
Full Title: Randomized, placebo-controlled, prospective clinical trial of efficacy and safety for the treatment of rhinitis/rhinoconjunctivitis and asthma against a mixture of Dermatophagoides pteronyssinus an... | |||||||||||||||||||||||
Medical condition: House dust mites allergy | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000971-97 | Sponsor Protocol Number: AL-X-01 | Start Date*: 2017-08-23 | |||||||||||
Sponsor Name:ALK Abelló A/S | |||||||||||||
Full Title: Safety and tolerability of shortened up-dosing with Alutard SQ | |||||||||||||
Medical condition: Allergic rhinoconjunctivitis induced by grass pollen, birch pollen and house dust mites | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003634-14 | Sponsor Protocol Number: 107-PR-PRI-185 | Start Date*: 2012-02-17 | |||||||||||
Sponsor Name:Laboratorios Leti, S.L.Unipersonal | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (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: 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: 2013-000487-28 | Sponsor Protocol Number: VO72.12 | Start Date*: 2013-08-20 | ||||||||||||||||
Sponsor Name:STALLERGENES SA | ||||||||||||||||||
Full Title: A dose ranging study investigating the efficacy and safety of sublingual immunotherapy tablets of house dust mite allergen extracts in adults with house dust mite-associated allergic asthma | ||||||||||||||||||
Medical condition: house dust mite-associated allergic asthma | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) GB (Completed) SK (Completed) DE (Completed) CZ (Completed) BE (Completed) ES (Ongoing) PL (Completed) BG (Completed) DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003516-62 | Sponsor Protocol Number: CYT003-QbG10 08 | Start Date*: 2007-10-19 | |||||||||||
Sponsor Name:Cytos Biotechnology AG | |||||||||||||
Full Title: Double-blind, Placebo-controlled Study to Investigate an Immunomodulatory Therapy (CYT003-QbG10) in Adult Patients with Perennial Allergic Rhinoconjunctivitis. | |||||||||||||
Medical condition: Adult patients with perennial allergic rhinoconjunctivitis | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) LT (Completed) LV (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003427-11 | Sponsor Protocol Number: PRO-RCT-ACAROS-2018-01 | Start Date*: 2021-09-15 | |||||||||||
Sponsor Name:Probelte Pharma S.L.U. | |||||||||||||
Full Title: Efficacy and safety assessment of a subcutaneous immunotherapy (Beltavac®) with polymerized allergenic extract from house dust mites in patients with allergic rhinitis/rhinoconjuntivitis | |||||||||||||
Medical condition: Allergic rhinitis/ rhinoconjuntivitis associated or not with asthma | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 2009-014036-37 | Sponsor Protocol Number: AL0907ac | Start Date*: Information not available in EudraCT | ||||||||||||||||
Sponsor Name:Allergopharma Joachim Ganzer KG | ||||||||||||||||||
Full Title: A multicentre randomised placebo-controlled double-blind clinical trial for evaluation of safety and efficacy of a specific immunotherapy with an aluminium hydroxide adsorbed allergoid preparation ... | ||||||||||||||||||
Medical condition: Immunoglobulin E (IgE)-mediated allergic disease in adults and adolescents manifested by allergic rhinitis/rhinoconjunctivitis with or without controlled allergic asthma bronchiale (Global Initiati... | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: PL (Prematurely Ended) BG (Prematurely Ended) ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-000560-22 | Sponsor Protocol Number: MT-12 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:ALK-Abelló A/S | |||||||||||||
Full Title: A one-year placebo-controlled phase III trial evaluating the efficacy and safety of the house dust mite (HDM) SLIT-tablet in children (5-11 years of age) with HDM allergic rhinitis/rhinoconjunctivi... | |||||||||||||
Medical condition: Allergic rhinitis/rhinoconjunctivitis induced by house dust mites | |||||||||||||
|
|||||||||||||
Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) SK (Completed) DE (Completed) PL (Completed) ES (Ongoing) BG (Completed) LT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006261-81 | Sponsor Protocol Number: PM/0028 | Start Date*: 2009-06-24 | ||||||||||||||||||||||||||
Sponsor Name:HAL Allergy | ||||||||||||||||||||||||||||
Full Title: Dose Tolerability Study with High Dose PURETHAL Mites in Allergic Rhinitis / Rhinoconjunctivitis Patients. An open study to assess tolerability, safety and short-term efficacy of high dose PURETHA... | ||||||||||||||||||||||||||||
Medical condition: Allergic (IgE-mediated) rhinitis / rhinoconjunctivitis triggered by house dust mites. | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
