- Trials with a EudraCT protocol (11)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (6)
		
	   		
	   		    
                    
                   	
                   	    11 result(s) found for: Pyoderma.
                    
                
			
   			
		
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| EudraCT Number: 2008-008291-14 | Sponsor Protocol Number: UKDCTN0901 | Start Date*: 2009-05-14 | ||||||||||||||||
| Sponsor Name:Nottingham University Hospitals NHS Trust | ||||||||||||||||||
| Full Title: Study of treatments in Pyoderma Gangrenosum patients | ||||||||||||||||||
| Medical condition: pyoderma gangrenosum | ||||||||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) IE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2015-000762-65 | Sponsor Protocol Number: CAIN457ADE01T | Start Date*: 2015-07-09 | |||||||||||
| Sponsor Name:Technische Universität München, School of Medicine, represented by Dean | |||||||||||||
| Full Title: Single-arm study to assess a potential effect of anti-IL-17 (Secukinumab) in the treatment of pyoderma gangrenosum | |||||||||||||
| Medical condition: Pyoderma gangrenosum is an autoinflammatory disease, characterized by relapsing, painful ulcers of the skin. Treatment of PG is difficult. Patients suffer from long hospitalization, pain and redu... | |||||||||||||
| 
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-003273-21 | Sponsor Protocol Number: IFX-1-P2.7 | Start Date*: 2020-11-09 | |||||||||||
| Sponsor Name:InflaRx GmbH | |||||||||||||
| Full Title: Open label exploratory phase IIa trial to investigate the safety and efficacy of IFX-1 in treating subjects with Pyoderma Gangrenosum (OPTIMA). | |||||||||||||
| Medical condition: Pyoderma gangrenosum | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-002920-41 | Sponsor Protocol Number: StelaraPG01 | Start Date*: 2012-01-04 | |||||||||||
| Sponsor Name:University Hospital Tübingen | |||||||||||||
| Full Title: Open-label Trial of Stelara® (Ustekinumab) In Patients with Pyoderma gangrenosum – an open, non-placebo controlled pilot study with 10 patients. | |||||||||||||
| Medical condition: Patients with a clinical diagnosis of Pyoderma gangrenosum | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-006013-11 | Sponsor Protocol Number: HOTPANTS | Start Date*: 2022-08-29 | 
| Sponsor Name:Erasmus MC, department of dermatology | ||
| Full Title: Hyperbaric Oxygen Therapy for Pyoderma gangrenosum As a New Treatment Strategy | ||
| Medical condition: Pyoderma gangrenosum | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-002249-53 | Sponsor Protocol Number: P150924 | Start Date*: 2023-02-16 | |||||||||||
| Sponsor Name:Assistance Publique - Hôpitaux de Paris (AP-HP) | |||||||||||||
| Full Title: Comparing short to standard amoxicillin course for eRysipElas: a non-inferiority randomized controlled trial | |||||||||||||
| Medical condition: Adults diagnosed with lower limbs erysipelas/ cellulitis | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-005754-28 | Sponsor Protocol Number: PAPA-Can | Start Date*: 2023-07-10 | ||||||||||||||||||||||||||
| Sponsor Name:IRCCS ISTITUTO GIANNINA GASLINI | ||||||||||||||||||||||||||||
| Full Title: A double-blind, placebo-controlled, randomized withdrawal study of canakinumab in pyogenic sterile arthritis pyoderma gangrenosum and acne (PAPA) syndrome | ||||||||||||||||||||||||||||
| Medical condition: PAPA syndrome (Pyogenic Arthritis, Pyoderma gangrenosum and Acne) | ||||||||||||||||||||||||||||
| 
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: IT (Trial now transitioned) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2014-001276-56 | Sponsor Protocol Number: AIDA | Start Date*: 2014-07-11 | 
| Sponsor Name:North Bristol NHS - Southmead Hospital | ||
| Full Title: A prospective, open label, randomised controlled clinical trial, with pharmacokinetic-pharmacodynamic validation, to compare antimicrobial treatment with oral minocycline plus rifampicin to treatme... | ||
| Medical condition: Complicated Skin and Skin Structure infections caused by Methicillin Resistant Staphylococcus Aureus | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: IT (Completed) GR (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-004860-78 | Sponsor Protocol Number: P1209NY | Start Date*: 2014-05-09 | |||||||||||
| Sponsor Name:G. Pohl-Boskamp GmbH & Co. KG | |||||||||||||
| Full Title: A randomised, active-controlled, observer-blind, non-inferiority study to investigate the efficacy, safety and tolerability of a local treatment with dimeticone-based pediculicides in head lice inf... | |||||||||||||
| Medical condition: Pediculosis capitis | |||||||||||||
| 
 | |||||||||||||
| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-005281-30 | Sponsor Protocol Number: DUR001-306 | Start Date*: 2016-11-03 | ||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Allergan Ltd. | ||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: A Phase 3, Multicenter, Open-Label, Randomized, Comparator Controlled Trial of the Safety and Efficacy of Dalbavancin versus Active Comparator in Pediatric Subjects with Acute Bacterial Skin and Sk... | ||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Acute bacterial skin and skin structure infection. For Cohort 5 (from birth to less than 3 months) also patients with sepsis are allowed. | ||||||||||||||||||||||||||||||||||||||||||||||||
| 
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| Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: LV (Prematurely Ended) LT (Prematurely Ended) ES (Prematurely Ended) BG (Completed) GR (Completed) PL (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2016-003797-40 | Sponsor Protocol Number: APD334-006 | Start Date*: 2017-02-23 | 
| Sponsor Name:Arena Pharmaceuticals, Inc. | ||
| Full Title: A Phase 2a, Proof of Concept, Open-label Study Evaluating the Efficacy and Safety of Etrasimod (APD334) in Inflammatory Bowel Disease Patients with active Skin Extra-intestinal Manifestations | ||
| Medical condition: Active Skin Extra-Intestinal Manifestations in Inflammatory Bowel Disease. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) DE (Completed) | ||
| Trial results: View results | ||
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