- Trials with a EudraCT protocol (407)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
407 result(s) found for: Bronchial diseases.
Displaying page 1 of 21.
EudraCT Number: 2010-023945-31 | Sponsor Protocol Number: PRINA | Start Date*: 2010-12-17 |
Sponsor Name:AZIENDA OSPEDALIERA S. PAOLO (A.O. DI RILIEVO NAZIONALE) | ||
Full Title: Effect of Prasugrel sull'iperreattivita' bronchial and markers of airway inflammation in patients with chronic asthma: randomized crossover pilot study (Study PRINA). | ||
Medical condition: bronchial asthma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-001572-22 | Sponsor Protocol Number: PDY14192 | Start Date*: 2015-12-01 | |||||||||||
Sponsor Name:SANOFI-AVENTIS RECHERCHE ET DEVELOPPEMENT | |||||||||||||
Full Title: An exploratory, randomized, double-blind, placebo-controlled study of the effects of dupilumab on airway inflammation of adults with persistent asthma | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) SE (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002151-26 | Sponsor Protocol Number: Z7200K02 | Start Date*: 2014-08-27 | ||||||||||||||||||||||||||
Sponsor Name:Zambon Spa | ||||||||||||||||||||||||||||
Full Title: A Double Blind, Double Dummy, Randomized, Two Way Cross-Over Study To Compare The Effects Of Z7200 And Symbicort® Turbohaler On Functional Respiratory Imaging Parameters In Asthmatic Patients | ||||||||||||||||||||||||||||
Medical condition: Asthma | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-005789-36 | Sponsor Protocol Number: FLUI-2012-94 | Start Date*: 2013-03-04 | ||||||||||||||||||||||||||
Sponsor Name:FluidDA nv | ||||||||||||||||||||||||||||
Full Title: Double blind, double dummy, randomized, two way cross-over study to compare the effects of Seretide® Evohaler (supplied by Allen & Hanburys, UK) and a generic test HFA pMDI (manufactured by Cipla L... | ||||||||||||||||||||||||||||
Medical condition: Asthma | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-002977-84 | Sponsor Protocol Number: BECRO/RESP/ANASSA-PD | Start Date*: 2020-10-16 | ||||||||||||||||
Sponsor Name:RESPIRENT Pharmaceuticals | ||||||||||||||||||
Full Title: A phase III, randomized, multicenter, parallel-group clinical trial for examining the therapeutic equivalence between Fluticasone propionate 100 mcg/blister oral inhalation powder/Respirent Pharmac... | ||||||||||||||||||
Medical condition: Asthma is a heterogeneous disease, usually characterized by chronic airway inflammation. It is defined by the history of respiratory symptoms such as wheeze, shortness of breath, chest tightness an... | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000372-42 | Sponsor Protocol Number: FSJD-ALINO-2011 | Start Date*: 2012-07-23 | |||||||||||
Sponsor Name:Fundació per la Recerca i la Docència Sant Joan de Déu | |||||||||||||
Full Title: A Phase IV, open-label, prospective, randomised clinical trial to evaluate the usefulness of measuring nitric oxide in exhaled air in the therapeutic management of adult patients with mild asthma | |||||||||||||
Medical condition: Treatment in non-smoking adult patients with mild persistent atopic bronchial asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002276-27 | Sponsor Protocol Number: PVSD-ICS | Start Date*: 2016-08-04 | |||||||||||
Sponsor Name:Medisch Spectrum Twente | |||||||||||||
Full Title: The predictive value of the acute effect of beclomethasone-dipropionate on a mannitol challenge test for the outcome of longterm treatment with beclomethasone-dipropionate in childhood asthma | |||||||||||||
Medical condition: exercise induced bronchoconstriction asthma | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002816-97 | Sponsor Protocol Number: ADC3680-04 | Start Date*: 2011-09-22 | |||||||||||
Sponsor Name:Pulmagen Therapeutics LLP | |||||||||||||
Full Title: A Randomised, Placebo-Controlled, Double-Blind, Parallel Group Phase II Study to Assess the Safety, Tolerability and Pharmacokinetics of ADC3680B in Subjects with Partly Controlled Atopic Asthma | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000039-22 | Sponsor Protocol Number: CCD-1113-PR-0074 | Start Date*: 2012-06-05 | |||||||||||
Sponsor Name:CHIESI | |||||||||||||
Full Title: AN OPEN LABEL PLACEBO STUDY TO ASSESS THE INHALATION PROFILE OBTAINED BY ACOUSTIC MONITORING IN ASTHMATIC PATIENTS USING THE NEXTHALER DRY POWDER INHALER (DPI) DEVICE. | |||||||||||||
Medical condition: Adults asthmatics Patients with varying degrees of disease control. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002932-15 | Sponsor Protocol Number: 2014-002932-15 | Start Date*: 2014-09-10 | |||||||||||
Sponsor Name:Bispebjerg University Hospital | |||||||||||||
Full Title: The effect of inhaled glucocorticoids on the content of Na+/K+ pumps in human skeletal muscle | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000512-25 | Sponsor Protocol Number: MC/PR/033011/004/05 | Start Date*: 2006-04-20 | |||||||||||
Sponsor Name:CHIESI | |||||||||||||
Full Title: DOUBLE BLIND, DOUBLE DUMMY, RANDOMISED, PARALLEL GROUP, MONOCENTRIC CLINICAL TRIAL ON THE EFFECTS OF CHF 1535 MDI OR SERETIDE DPI ON BIOLOGICAL AND FUNCTIONAL MARKERS OF SMALL AIRWAYS IN PATIENTS W... | |||||||||||||
Medical condition: ASTHMA | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002705-38 | Sponsor Protocol Number: 3103013 | Start Date*: 2014-11-18 | ||||||||||||||||
Sponsor Name:Orion Corporation Orion Pharma | ||||||||||||||||||
Full Title: STUDY COMPARING BRONCHODILATOR EFFICACY OF TWO DRY POWDER INHALERS, BUDESONIDE/FORMOTEROL EASYHALER AND SYMBICORT TURBUHALER; A RANDOMISED, DOUBLE-BLIND, DOUBLE-DUMMY, MULTICENTRE, SINGLE DOSE, CRO... | ||||||||||||||||||
Medical condition: Asthma | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Completed) BG (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-005534-12 | Sponsor Protocol Number: AVH-2004/1 | Start Date*: 2006-04-18 |
Sponsor Name:The Symbio Herborn Group GmbH | ||
Full Title: randomized double blind placebo controlled study on the efficacy of autologous autovaccine in house dust mite allergy | ||
Medical condition: Allergic diseases such as rhinoconjunctivitis or bronchial asthma are a major public health burden. The huge associated costs demand an evidence based therapeutic aproach. The only available causat... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003683-31 | Sponsor Protocol Number: CQGE031B2201E1 | Start Date*: 2014-01-23 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: An open-label, multi-center, extension study to evaluate the long-term safety of subcutaneous 240mg QGE031 given every 4 weeks for 52 weeks in allergic asthma patients who completed study CQGE031B2201 | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Prematurely Ended) CZ (Prematurely Ended) PL (Prematurely Ended) FI (Prematurely Ended) HU (Completed) DE (Completed) IT (Prematurely Ended) PT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002298-69 | Sponsor Protocol Number: CQGE031B2201 | Start Date*: 2013-01-25 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A Multi-Center, Randomized, Double Blind, Placebo and Active-Controlled study with exploratory dose-ranging, to investigate the efficacy and safety of 16 weeks treatment with subcutaneous QGE031 in... | |||||||||||||
Medical condition: asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) SK (Completed) CZ (Completed) PT (Completed) GB (Completed) HU (Completed) IT (Completed) DE (Completed) PL (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003894-27 | Sponsor Protocol Number: TUD-HeHe01-055 | Start Date*: 2012-03-15 | |||||||||||
Sponsor Name:Technische Universität Dresden | |||||||||||||
Full Title: Tolerance and effect of an add-on therapy with an ivy leaves dry extract syrup on lung function in children with asthma. | |||||||||||||
Medical condition: Pediatric patients age 6-12 yrs with uncontrolled mild persistent asthma | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004940-36 | Sponsor Protocol Number: EFC13579 | Start Date*: 2015-07-20 | |||||||||||
Sponsor Name:Sanofi-aventis Recherche & Développement | |||||||||||||
Full Title: A Randomized, Double Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Efficacy and Safety of Dupilumab in Patients with Persistent Asthma | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) Outside EU/EEA IT (Completed) DE (Completed) ES (Completed) PL (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003479-22 | Sponsor Protocol Number: 200860 | Start Date*: 2016-11-09 | |||||||||||
Sponsor Name:GlaxoSmithKline Research and development Ltd | |||||||||||||
Full Title: Clinical assessment of fluticasone propionate/ salmeterol xinafoate HFA MDI in 6-month to 4-year-old Japanese patients with bronchial asthma | |||||||||||||
Medical condition: bronchial asthma | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003155-57 | Sponsor Protocol Number: CQGE031B2204 | Start Date*: 2015-11-03 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A Multi-Center, Randomized, Double-Blind, Placebo-Controlled study to investigate the efficacy and safety of 52 weeks treatment with QGE031 s.c. in Asthma Patients not adequately controlled by medi... | |||||||||||||
Medical condition: Severe Asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) HU (Completed) IT (Prematurely Ended) DE (Prematurely Ended) BE (Prematurely Ended) ES (Prematurely Ended) SK (Prematurely Ended) NL (Prematurely Ended) LU (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001442-16 | Sponsor Protocol Number: CCD-05993AB1-02 | Start Date*: 2014-11-12 | |||||||||||
Sponsor Name:Chiesi Farmaceutici S.p.A. | |||||||||||||
Full Title: A MULTICENTRE, RANDOMISED, DOUBLE-BLIND, PLACEBO-CONTROLLED, 2-WAY CROSS-OVER STUDY TO EVALUATE THE EFFICACY AND SAFETY OF CHF 5259 (GLYCOPYRROLATE BROMIDE) pMDI ON TOP OF QVAR® pMDI FOR THE TRE... | |||||||||||||
Medical condition: uncontrolled asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) PL (Completed) BG (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
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