- Trials with a EudraCT protocol (5)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
		
	   		
	   		    
                    
                   	
                   	    5 result(s) found for: Malassezia.
                    
                
			
   			
		
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| EudraCT Number: 2005-000785-39 | Sponsor Protocol Number: KETO 02/04 | Start Date*: 2005-09-21 | |||||||||||
| Sponsor Name:MIPHARM | |||||||||||||
| Full Title: Efficacy and Tolerability of Ketomousse, Ketoconazole 1 , Salicilic Acid and Zinc phyritione thermolabile foam in the treatment of Pityriasis Versicolor in comparison with Ketoconazole 2 cream ... | |||||||||||||
| Medical condition: PITYRIASIS VERSICOLOR | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-000552-27 | Sponsor Protocol Number: ACO2008-CT-01 | Start Date*: 2008-06-11 | 
| Sponsor Name:ACO HUD NORDIC AB | ||
| Full Title: Effect of moisturizing creams on skin barrier function and prevention of Malassezia recurrence in patients with atopic eczema | ||
| Medical condition: Dry skin barrier disorders such as atopic eczema and ichtyosis | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-004852-11 | Sponsor Protocol Number: BT0400-207-INT | Start Date*: 2006-02-07 | |||||||||||
| Sponsor Name:Barrier Therapeutics Inc. | |||||||||||||
| Full Title: A double-blind, randomized, placebo-controlled, dose finding study of R126638 given as a single or repeat dose in oral solution vs placebo in the treatment of pityriasis versicolor. | |||||||||||||
| Medical condition: Pityriasis versicolor / Tinea versicolor | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-000720-19 | Sponsor Protocol Number: IDI01/2020 | Start Date*: 2020-07-22 | |||||||||||
| Sponsor Name:IDI FARMACEUTICI SRL | |||||||||||||
| Full Title: A prospective, randomized, multicenter, open- label, two-arm and parallel-group Study to evaluate the efficacy and safety of Nicotinamide DS compared to Ciclopirox olamine cream at 1% in patients a... | |||||||||||||
| Medical condition: Patients affected by seborrheic dermatitis. | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-006208-21 | Sponsor Protocol Number: ELKE-2006 | Start Date*: 2006-10-23 | 
| Sponsor Name:Department of Dermatology, University of Kiel | ||
| Full Title: Clinical Efficacy of Pimecrolimus Cream in Seborrheic Dermatitis. Efficacy of pimecrolimus in normalizing clinical symptoms, explorative study of barrier function, hydration, lipid content and diff... | ||
| Medical condition: Efficacy of pimecrolimus in normalizing clinical symptoms, explorative study of barrier function, hydration, lipid content and differentiation in seborrheic dermatitis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: (No results available) | ||
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