- Trials with a EudraCT protocol (127)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
127 result(s) found for: Severe Persistent Asthma AND Asthma.
Displaying page 1 of 7.
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: 2005-000532-25 | Sponsor Protocol Number: D5890L00014 | Start Date*: 2005-06-15 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A comparison of Symbicort Single inhaler Therapy (Symbicort Turbuhaler 160/4.5 mg, 1 inhalation b.i.d. plus as needed) and conventional best practice for the treatment of persistent asthma in adole... | |||||||||||||
Medical condition: This is a Phase IIIB trial to be conducted in patients with persistent asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IS (Completed) LT (Completed) LV (Completed) CZ (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001681-40 | Sponsor Protocol Number: BY9010/IT-101 incl. amendment 1 | Start Date*: 2004-10-25 | |||||||||||
Sponsor Name:ALTANA Pharma AG | |||||||||||||
Full Title: Comparison of inhaled ciclesonide (640 µg/day) and fluticasone propionate (1000 µg/day) in patients with moderate and severe per-sistent asthma | |||||||||||||
Medical condition: asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005030-19 | Sponsor Protocol Number: VR506/2/004 | Start Date*: 2012-08-17 | |||||||||||
Sponsor Name:Vectura Limited | |||||||||||||
Full Title: A randomised double-blind, parallel group, dose-ranging study to evaluate the efficacy and safety of three different total daily doses of fluticasone propionate inhaled from a new dry powder inhale... | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) HU (Completed) PL (Completed) BG (Completed) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000520-18 | Sponsor Protocol Number: CQMF149E2203 | Start Date*: 2012-10-18 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A multicenter, randomized, double-blind, placebo controlled, 12-week treatment, parallel-group study to assess the efficacy, safety and pharmacokinetics of indacaterol acetate (75 and 150 μg o.d.) ... | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) SK (Completed) DE (Completed) BG (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006512-30 | Sponsor Protocol Number: D5890L00022 | Start Date*: 2007-01-15 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Pan-European, open label, randomised study comparing the efficacy and cost-effectiveness of Symbicort Maintenance and Reliever Therapy (Symbicort SMART) using a maintenance dose of Symbicort 160/... | |||||||||||||
Medical condition: Persistent asthma. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) GR (Completed) IS (Completed) NL (Completed) FR (Completed) ES (Completed) IE (Completed) DK (Completed) FI (Completed) BE (Completed) IT (Completed) DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002766-37 | Sponsor Protocol Number: 2003-72-DPI-6 | Start Date*: 2005-01-12 | |||||||||||
Sponsor Name:HEXAL AG (Project Management on behalf of the Sponsor: HEXAL Pharmaforschung GmbH | |||||||||||||
Full Title: Open-label, multi-center, non-controlled follow-up study over 3-months on the safety of Formoterol Easyhaler® in approximately 35 asthmatic pediatric patients initially treated in study 2003-51-DPI-2 | |||||||||||||
Medical condition: Moderate to severe asthma bronciale in pediatric | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004191-13 | Sponsor Protocol Number: AVT-01/2/AST/04 | Start Date*: 2007-01-23 | |||||||||||
Sponsor Name:Avontec GmbH | |||||||||||||
Full Title: Efficacy and safety of AVT-01 10 mg single dose in patients with mild asthma challenged with inhaled tumor necrosis factor alpha – A double-blind, randomized, placebo-controlled clinical study | |||||||||||||
Medical condition: Male outpatients aged 18 - 65 with moderate persistent atopic asthma | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001242-17 | Sponsor Protocol Number: BY9010/M1-207 | Start Date*: 2005-07-18 | |||||||||||
Sponsor Name:ALTANA Pharma AG | |||||||||||||
Full Title: Efficacy and Safety – Study by ALTANA on Ciclesonide in Pre-school Asthma Patients | |||||||||||||
Medical condition: asthma bronchiale | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) ES (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004932-20 | Sponsor Protocol Number: 1311.14 | Start Date*: 2015-06-05 |
Sponsor Name:SCS Boehringer Ingelheim Comm.V | ||
Full Title: A phase IIa, randomized, double-blind, placebo controlled, parallel group study to assess the safety and efficacy of subcutaneously administered BI 655066 (risankizumab) as add-on therapy over 24 w... | ||
Medical condition: Severe Asthma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) GB (Completed) HU (Completed) NL (Completed) DE (Completed) PL (Completed) IT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-005926-22 | Sponsor Protocol Number: FLT3501 | Start Date*: 2007-03-14 | |||||||||||
Sponsor Name:Mundipharma Research Ltd. | |||||||||||||
Full Title: An open, randomised, parallel group, multicentre study to compare the efficacy and safety of FlutiForm pMDI vs Seretide pMDI in adult subjects with mild to moderate-severe persistent, reversible as... | |||||||||||||
Medical condition: Asthma bronchial | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001514-33 | Sponsor Protocol Number: BUSAL-III-05-1 | Start Date*: 2006-06-05 | |||||||||||
Sponsor Name:Laboratories SMB S.A. | |||||||||||||
Full Title: A phase III, randomized, parallel group study to compare the therapeutic efficacy of SMB BUDESONIDE-SALMETEROL DPI capsule 300/25μg BID delivered by the AXAHALER® versus SERETIDE® DISKUS® 500/50μg ... | |||||||||||||
Medical condition: Diagnosis of moderate to severe persistent asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) EE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002078-45 | Sponsor Protocol Number: FG-506-17-05 | Start Date*: 2004-11-01 | |||||||||||
Sponsor Name:Fujisawa GmbH | |||||||||||||
Full Title: A RANDOMISED, DOUBLE-BLIND, PLACEBO CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF TACROLIMUS MDI AS ADD-ON THERAPY TO ICS AND LABA IN MODERATE TO SEVERE PERSISTENT ASTHMATIC PATIENTS | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007244-33 | Sponsor Protocol Number: LPA112046 | Start Date*: 2009-04-08 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: The efficacy of orally administered GSK2190915 as an add-on to current therapy in subjects with moderate to severe asthma who have elevated sputum neutrophils | |||||||||||||
Medical condition: Moderate to severe asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-002375-11 | Sponsor Protocol Number: EFC13995 | Start Date*: 2022-07-20 | |||||||||||
Sponsor Name:Sanofi-aventis recherche & développement | |||||||||||||
Full Title: A Randomized, Double Blind, Placebo-controlled, Parallel-group Phase 3 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: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001103-36 | Sponsor Protocol Number: 2013RC01 | Start Date*: 2013-05-27 | |||||||||||
Sponsor Name:Tayside Medical Sciences Centre on behalf of University of Dundee & NHS Tayside | |||||||||||||
Full Title: Randomised controlled single and chronic dosing crossover comparison of extra fine particle formoterol and coarse particle salmeterol in asthmatic patients with persistent small airways dysfunction | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001869-33 | Sponsor Protocol Number: D3551C00001 | Start Date*: 2013-01-18 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A 6-month, Randomised, Double-blind, Placebo-controlled, Multi-centre, Parallel-group, Phase II Study with an Optional Safety Extension Treatment Period up to 6 months, to Evaluate the Efficacy, Sa... | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) DE (Prematurely Ended) CZ (Prematurely Ended) HU (Prematurely Ended) PL (Prematurely Ended) SK (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002084-27 | Sponsor Protocol Number: cro-725 | Start Date*: 2007-10-02 | |||||||||||
Sponsor Name:Imperial College | |||||||||||||
Full Title: The pharmacokinetics and anti-inflammatory effects of prednisolone in severe asthma. | |||||||||||||
Medical condition: This study is designed to look why patients with severe asthma fail to respond to oral corticosteroids in the same way as patients with non-severe disease. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020803-63 | Sponsor Protocol Number: AB07015 | Start Date*: 2010-10-18 | |||||||||||
Sponsor Name:AB Science | |||||||||||||
Full Title: A prospective, multicenter, randomised, double-blind, placebo-controlled, 2-parallel groups, Phase 3 study to compare the efficacy and the safety of masitinib at 6 mg/kg/day versus placebo in the t... | |||||||||||||
Medical condition: Severe Persistent Asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prohibited by CA) CZ (Completed) BG (Completed) DE (Prematurely Ended) SK (Completed) ES (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000683-99 | Sponsor Protocol Number: CL-9709-301-RD | Start Date*: 2011-09-20 | |||||||||||
Sponsor Name:Takeda Development Centre Europe Ltd. | |||||||||||||
Full Title: Control of moderate or severe asthma with 160, 320 and 640μg ciclesonide/day. A one-year randomised, double-blind, multicenter trial. | |||||||||||||
Medical condition: moderate or severe asthma | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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