- Trials with a EudraCT protocol (391)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
391 result(s) found for: Moderate Asthma.
Displaying page 7 of 20.
| EudraCT Number: 2011-005512-28 | Sponsor Protocol Number: 205.443 | Start Date*: 2012-10-04 | |||||||||||
| Sponsor Name:Boehringer Ingelheim | |||||||||||||
| Full Title: A phase II/III, randomised, double-blind, placebo-controlled, parallel group trial to evaluate safety and efficacy of tiotropium inhalation solution (2.5 µg and 5 µg) administered once daily in the... | |||||||||||||
| Medical condition: Asthma | |||||||||||||
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| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) LT (Completed) LV (Completed) FI (Completed) DE (Completed) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-006077-27 | Sponsor Protocol Number: BS559 | Start Date*: 2006-06-26 | |||||||||||
| Sponsor Name:Merck Generics | |||||||||||||
| Full Title: A MULTICENTRE, DOUBLE-BLIND, DOUBLE-DUMMY, RANDOMISED, PARALLEL-GROUP STUDY TO DETERMINE THE THERAPEUTIC EQUIVALENCE BETWEEN FLUTICASONE PROPIONATE, 100 µg TWICE DAILY DELIVERED VIA A PRESSURISED M... | |||||||||||||
| Medical condition: Asthma | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) SK (Completed) HU (Completed) DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-005306-37 | Sponsor Protocol Number: D3741C00003 | Start Date*: 2015-05-27 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A randomized, double-blind, multiple dosing (14 days), placebo-controlled, incomplete block crossover, multi-center study to assess efficacy and safety of three dose levels of AZD7594, given once d... | |||||||||||||
| Medical condition: Patients with mild to moderate asthma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-021093-11 | Sponsor Protocol Number: 205.444 | Start Date*: 2010-11-13 | |||||||||||
| Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
| Full Title: A Phase III randomised, double blind, placebo-controlled, parallel group study to assess the efficacy and safety over 48 weeks of orally inhaled Tiotropium bromide (2.5 µg and 5 µg once daily ) del... | |||||||||||||
| Medical condition: moderate persistent asthma | |||||||||||||
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| Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: LV (Completed) HU (Completed) ES (Completed) SK (Completed) IT (Prematurely Ended) DE (Completed) NO (Ongoing) Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-001483-29 | Sponsor Protocol Number: CCD-1202-PR-0080 | Start Date*: 2012-08-08 | |||||||||||
| Sponsor Name:Chiesi Farmaceutici S.p.A. | |||||||||||||
| Full Title: A RANDOMISED, DOUBLE-BLIND, PLACEBO-CONTROLLED, THREE-WAY CROSSOVER STUDY TO EVALUATE THE EFFICACY AFTER ALLERGEN CHALLENGE, SAFETY, AND TOLERABILITY OF TWO DOSES OF INHALED CHF6001 DPI AFTER 9 DAY... | |||||||||||||
| Medical condition: asthma | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-013705-34 | Sponsor Protocol Number: D0540C00004 | Start Date*: 2009-10-05 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A double-blind, placebo controlled, randomised, parallel group, single centre, phase IIa study to investigate the efficacy, tolerability and safety of 8 doses of AZD8848 administered intranasally o... | |||||||||||||
| Medical condition: Allergic Asthma | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-006013-24 | Sponsor Protocol Number: OC000459/012/08 | Start Date*: 2009-03-25 | |||||||||||
| Sponsor Name:Oxagen Ltd. | |||||||||||||
| Full Title: Dose Finding Study in Patients with Mild to Moderate Persistent Asthma: A Parallel Group, Randomised, Placebo Controlled, Double Blind Assessment of Oral OC000459 Dosed at Three Dose Schedules for ... | |||||||||||||
| Medical condition: Mild to moderate persistent asthma | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-003338-35 | Sponsor Protocol Number: D7552C00001 | Start Date*: 2022-06-06 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A Phase 2, Randomised, Double-Blind, Placebo-Controlled Study to Assess Efficacy and Safety of Multiple Dose Levels of Atuliflapon Given Orally Once Daily for Twelve Weeks in Adults with Moderate-t... | |||||||||||||
| Medical condition: Moderate-to-Severe Uncontrolled Asthma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) PL (Trial now transitioned) HU (Trial now transitioned) BG (Trial now transitioned) SI (Trial now transitioned) SK (Trial now transitioned) NL (Trial now transitioned) IT (Prematurely Ended) RO (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-003663-35 | Sponsor Protocol Number: PBF-680CT-05 | Start Date*: 2018-06-13 | |||||||||||
| Sponsor Name:Palobiofarma S.L | |||||||||||||
| Full Title: A phase II, double-blind, randomized, parallel-group, placebocontrolled multi-center study to investigate the effect of the adenosine A1 receptor antagonist PBF-680 on forced expiratory volume in 1... | |||||||||||||
| Medical condition: patients with mild-to-moderate persistent atopic asthma | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-000865-29 | Sponsor Protocol Number: C38072-AS-30025 | Start Date*: 2015-10-01 | |||||||||||
| Sponsor Name:Teva Branded Pharmaceutical Products R&D, Inc. | |||||||||||||
| Full Title: A 52-Week Double-Blind, Placebo-Controlled, Parallel-Group Efficacy and Safety Study of Reslizumab 110 mg Fixed, Subcutaneous Dosing in Patients with Uncontrolled Asthma and Elevated Blood Eosinophils | |||||||||||||
| Medical condition: Uncontrolled Asthma & elevated blood Eosinophils | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) ES (Prematurely Ended) HU (Prematurely Ended) BE (Completed) PL (Prematurely Ended) DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-003395-40 | Sponsor Protocol Number: O-AV | Start Date*: 2012-10-04 | |||||||||||
| Sponsor Name:Watson Laboratories, Inc. | |||||||||||||
| Full Title: Double-blind, masked, randomized, three period crossover study to evaluate the changes in exhaled nitric oxide (eNO) following treatment with fluticasone propionate MDI Aerosol in patients with chr... | |||||||||||||
| Medical condition: Chronic mild to moderate persistent asthma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-000188-15 | Sponsor Protocol Number: AL1402ac | Start Date*: 2017-01-09 | |||||||||||||||||||||
| Sponsor Name:Allergopharma GmbH & Co. KG | |||||||||||||||||||||||
| Full Title: A multicenter randomized double-blind placebo-controlled clinical trial for evaluation of efficacy and safety of specific immunotherapy with an aluminium hydroxide-adsorbed allergoid preparation o... | |||||||||||||||||||||||
| Medical condition: allergic bronchial asthma and allergic rhinitis or rhinoconjunctivitis | |||||||||||||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: PL (Completed) LT (Completed) DE (Completed) ES (Completed) LV (Completed) AT (Completed) HR (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2010-022458-18 | Sponsor Protocol Number: 205.425 | Start Date*: 2011-05-23 | |||||||||||
| Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
| Full Title: A phase II randomised, double-blind, placebo-controlled incomplete cross-over trial with 4-week treatment periods to evaluate efficacy and safety of tiotropium inhalation solution (doses of 1.25 μg... | |||||||||||||
| Medical condition: Moderate persistent asthma in children 6 to 11 years old | |||||||||||||
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| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) LV (Completed) LT (Completed) HU (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-000135-26 | Sponsor Protocol Number: 2006-04-DOS-2 | Start Date*: 2007-06-08 | |||||||||||
| Sponsor Name:Hexal AG | |||||||||||||
| Full Title: Double-blind, double-dummy, multi-center, randomized parallel group trial to demonstrate therapeutic equivalence of Salmeterol/Fluticasone MDI HEXAL (25 µg/50 µg per actuation) versus SeretideTM 50... | |||||||||||||
| Medical condition: Persistent, moderate asthma | |||||||||||||
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| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: LT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-000134-39 | Sponsor Protocol Number: 2006-03-DOS-1 | Start Date*: 2007-04-19 | |||||||||||
| Sponsor Name:Hexal AG | |||||||||||||
| Full Title: Double-blind, double-dummy, multi-center, randomized parallel group trial to demonstrate therapeutic equivalence of Salmeterol/Fluticasone MDI HEXAL (25 µg/125 µg per actuation) versus SeretideTM 1... | |||||||||||||
| Medical condition: persistent moderate asthma | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: LT (Completed) HU (Completed) PL (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-003103-39 | Sponsor Protocol Number: AR003 | Start Date*: 2007-04-19 | ||||||||||||||||
| Sponsor Name:University of Glasgow & Greater Glasgow Health Board | ||||||||||||||||||
| Full Title: Effect of statins on asthma control and airway inflammation in smokers with asthma | ||||||||||||||||||
| Medical condition: Chronic Asthma (smokers),COPD. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2017-001532-19 | Sponsor Protocol Number: 206821 | Start Date*: 2018-09-11 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
| Full Title: A randomised open-label study to compare the effectiveness of the fixed dose combination of FF/UMEC/VI (using the Connected Inhaler System) with the combination of FP/SAL plus tiotropium (without t... | |||||||||||||
| Medical condition: Inadequately controlled asthma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-001029-84 | Sponsor Protocol Number: AL0702rB | Start Date*: 2007-08-30 | ||||||||||||||||
| Sponsor Name:Allergopharma Joachim Ganzer KG | ||||||||||||||||||
| Full Title: A multicentre randomised, placebo-controlled, double-blind pivotal clinical trial for the evaluation of safety and efficacy of specific of immunotherapy with an aluminium hydroxide-adsorbed hypoall... | ||||||||||||||||||
| Medical condition: ICD classification code: J45.0 and J30.1 | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) SE (Completed) FI (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2018-004381-33 | Sponsor Protocol Number: CQAW039A2127 | Start Date*: 2019-12-11 | |||||||||||
| Sponsor Name:Novartis Pharma AG | |||||||||||||
| Full Title: Randomized, subject and investigator blinded, placebo-controlled study to demonstrate the anti-inflammatory effect of fevipiprant (QAW039) in moderate-severe asthma patients with high sputum and... | |||||||||||||
| Medical condition: Asthma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) FR (Prematurely Ended) DE (Prematurely Ended) ES (Prematurely Ended) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-017223-25 | Sponsor Protocol Number: FLT3507 | Start Date*: 2010-04-01 | |||||||||||
| Sponsor Name:Mundipharma Research Ltd | |||||||||||||
| Full Title: A double blind, double dummy, randomised, multicentre, two arm parallel group study to assess the efficacy and safety of FlutiForm® pMDI 125/5 µg (2 puffs bid) vs Symbicort® Turbohaler® 200/6 µg (2... | |||||||||||||
| Medical condition: Asthma bronchial | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Completed) HU (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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