- Trials with a EudraCT protocol (6)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
6 result(s) found for: Ear mites.
Displaying page 1 of 1.
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: 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 | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000585-41 | Sponsor Protocol Number: OG-061-01 | Start Date*: 2020-11-06 | ||||||||||||||||
Sponsor Name:T-Balance Therapeutics GmbH | ||||||||||||||||||
Full Title: Effects of tregalizumab on allergen-induced airway responses and airway inflammation in asthmatic patients | ||||||||||||||||||
Medical condition: mild controlled allergic asthma and house-dust mite (HDM) allergy | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-000393-61 | Sponsor Protocol Number: PM/0037 | Start Date*: 2011-08-23 | |||||||||||
Sponsor Name:HAL Allergy B.V. | |||||||||||||
Full Title: A multi-centre, randomized, double-blind, placebo-controlled, dose range finding study to identify the optimal (i.e. safe and effective) dose of PURETHAL® Mites SCIT in patients with house dust mit... | |||||||||||||
Medical condition: Persistent allergic rhinitis or rhinoconjunctivitis with or without concomitant mild to moderate asthma induced by house dust mite (HDM) allergy (or sensitization). | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) NL (Completed) ES (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021170-11 | Sponsor Protocol Number: MOP4843g | Start Date*: 2011-01-19 | |||||||||||
Sponsor Name:GENENTECH, Inc. | |||||||||||||
Full Title: A PHASE II, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY, SAFETY, AND TOLERABILITY OF INTRAVENOUS MEMP1972A IN THE PREVENTION OF ALLERGEN... | |||||||||||||
Medical condition: asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001662-94 | Sponsor Protocol Number: TH005 | Start Date*: 2014-09-16 | |||||||||||
Sponsor Name:Circassia Ltd. | |||||||||||||
Full Title: A Double-Blind, Randomised, Placebo-Controlled, Multi-Centre Field Study to Assess the Efficacy and Safety of HDM-SPIRE in Subjects with a History of House Dust Mite-Induced Rhinoconjunctivitis | |||||||||||||
Medical condition: House Dust Mite-Induced Rhinoconjunctivitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) DE (Completed) NL (Completed) LT (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
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