- Trials with a EudraCT protocol (4)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
		
	   		
	   		    
                    
                   	
                   	    4 result(s) found for: Aminophylline.
                    
                
			
   			
		
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| EudraCT Number: 2014-000182-45 | Sponsor Protocol Number: 2013AT001B | Start Date*: 2014-04-02 | |||||||||||
| Sponsor Name:Royal Brompton and Harefield NHS Foundation Trust | |||||||||||||
| Full Title: A pilot study into health pre and post treatment with intravenous Aminophylline and Hydrocortisone in severe asthmatics | |||||||||||||
| Medical condition: Severe asthma | |||||||||||||
| 
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-004749-28 | Sponsor Protocol Number: MK-0476-334 | Start Date*: 2015-04-03 | 
| Sponsor Name:Banyu Pharmaceutical Co., Ltd. | ||
| Full Title: MK-476 Phase III Open Label Exploratory Comparative Study -Acute Exacerbations of Asthma- Protocol number: 334 | ||
| Medical condition: Acute Exacerbations of Asthma | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2004-001065-18 | Sponsor Protocol Number: BY217/M2-015 incl. Amendment No1 | Start Date*: 2004-10-04 | |||||||||||
| Sponsor Name:ALTANA Pharma AG | |||||||||||||
| Full Title: Morning versus evening administration of 500µg Roflumilast once dailyfor 6 weeks in patients with asthma. | |||||||||||||
| Medical condition: Asthma | |||||||||||||
| 
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (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 | |||||||||||||
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