- Trials with a EudraCT protocol (7)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
7 result(s) found for: Eotaxin 3.
Displaying page 1 of 1.
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: 2007-003971-38 | Sponsor Protocol Number: 0476-374 | Start Date*: 2007-10-03 | ||||||||||||||||
Sponsor Name:Laboratoires Merck Sharp & Dohme - Chibret | ||||||||||||||||||
Full Title: An Observational Follow-Up Study of Pediatric Patients Who Participated in a Previous Respiratory Syncytial Virus (RSV)-Induced Bronchiolitis Study of Montelukast | ||||||||||||||||||
Medical condition: asthma and atopic diseases | ||||||||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) ES (Completed) DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-001722-66 | Sponsor Protocol Number: REP_COVID | Start Date*: 2020-04-23 | ||||||||||||||||
Sponsor Name:Fundació Clínic per a la recerca Biomèdica | ||||||||||||||||||
Full Title: Plasma turnover in patients with COVID-19 disease and invasive mechanical ventilation: a randomized study | ||||||||||||||||||
Medical condition: coronavirus (covid-19) infection with respiratory failure requiring mechanical ventilation. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004499-23 | Sponsor Protocol Number: LIVERHOPE_SAFETY | Start Date*: 2017-03-10 | |||||||||||
Sponsor Name:IDIBAPS | |||||||||||||
Full Title: Safety and tolerability of the combination of simvastatin plus rifaximin in patients with decompensated cirrhosis: a multicenter, double-blind, placebo controlled randomized clinical trial. | |||||||||||||
Medical condition: Patients with decompensated cirrhosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) NL (Completed) GB (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001143-31 | Sponsor Protocol Number: 37725 | Start Date*: 2013-07-08 | |||||||||||
Sponsor Name:Bispebjerg University Hospital | |||||||||||||
Full Title: TARGET “Targeting the small airways in asthma” Does fine particle ICS improve peripheral airway inflammation and function in patients with insufficient response to large particle ICS? | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003689-26 | Sponsor Protocol Number: CLS001-CO-PR-00;CHDR1428 | Start Date*: 2015-04-16 | ||||||||||||||||
Sponsor Name:Cutanea Life Sciences | ||||||||||||||||||
Full Title: A randomized, double-blind, placebo controlled study to assess the pharmacodynamics, safety/tolerability and efficacy of omiganan in patients with mild to moderate atopic dermatitis | ||||||||||||||||||
Medical condition: Patients with mild to moderate atopic dermatitis. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005036-26 | Sponsor Protocol Number: FXT-05 | Start Date*: 2011-11-29 | ||||||||||||||||||||||||||
Sponsor Name:Funxional Therapeutics Ltd | ||||||||||||||||||||||||||||
Full Title: An Exploratory Phase IIa Study to Investigate the Biological Activity of Oral FX125L in Adult Patients with Chronic Inflammatory Disease | ||||||||||||||||||||||||||||
Medical condition: Asthma Chronic obstructive pulmonary disease Rheumatoid arthritis Psoriasis | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
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