- Trials with a EudraCT protocol (16)
 - Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
 
		
	   		
	   		    
                    
                   	
                   	    16 result(s) found for: Collagenase clostridium histolyticum.
                    
                
			
   			
		
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| EudraCT Number: 2018-003637-14 | Sponsor Protocol Number: AGO/2018/004 | Start Date*: 2019-03-29 | |||||||||||
| Sponsor Name:Ghent University Hospital | |||||||||||||
| Full Title: Local injection of collagenase clostridium histolyticum (XiapexR) for refractory gastrointestinal strictures: an open-label pilot study. | |||||||||||||
| Medical condition: refractory iatrogenic gastrointestinal strictures | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-000494-67 | Sponsor Protocol Number: 1.2 | Start Date*: 2013-10-22 | |||||||||||
| Sponsor Name:Klinik for håndkirurgi, Gentofte hospital | |||||||||||||
| Full Title: Needle fasciotomi vs collagenase for treatment of Dupuytrens contracture in 2nd, 3rd, 4th and 5th metacarpophalangeal joint. | |||||||||||||
| Medical condition: Dupuytrens contracture | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-005384-66 | Sponsor Protocol Number: AUX-CC-807 | Start Date*: 2014-04-28 | 
| Sponsor Name:Endo Ventures Limited | ||
| Full Title: A phase 3b, open-label pilot study to evaluate the safety and effectiveness of up to four treatment cycles of AA4500 in combination with the ErecAid® Esteem® Manual Vacuum Therapy System in men wit... | ||
| Medical condition: Peyronie's Disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-005065-21 | Sponsor Protocol Number: AUX-CC-862 | Start Date*: 2012-03-26 | |||||||||||
| Sponsor Name:Auxilium UK Limited | |||||||||||||
| Full Title: Retreatment of recurrent contractures in joints effectively treated with AA4500 (collagenase clostridium histolyticum [XIAFLEX®/XIAPEX®]) in an Auxilium-sponsored Phase 3 Study in the United States... | |||||||||||||
| Medical condition: Dupuytren's contracture | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-019888-10 | Sponsor Protocol Number: B1531002 | Start Date*: 2010-11-10 | |||||||||||
| Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, NY 10017 | |||||||||||||
| Full Title: PROSPECTIVE OPEN-LABEL INVESTIGATION OF THE NON-SURGICAL TREATMENT WITH COLLAGENASE CLOSTRIDIUM HISTOLYTICUM (XIAPEX®) | |||||||||||||
| Medical condition: Dupuytren’s contracture | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) HU (Completed) ES (Completed) SE (Completed) DK (Completed) DE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-005215-41 | Sponsor Protocol Number: 5.5 | Start Date*: 2017-05-05 | |||||||||||
| Sponsor Name:Olli Leppänen | |||||||||||||
| Full Title: DupuytrEn Treatment EffeCtiveness Trial (DETECT): a protocol for prospective, randomized, controlled, outcome assessor-blinded, three armed parallel 1:1:1, multicenter trial comparing efficacy and ... | |||||||||||||
| Medical condition: | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-000516-28 | Sponsor Protocol Number: 39032 | Start Date*: 2012-06-14 | 
| Sponsor Name:University Medical Centre Groningen | ||
| Full Title: A prospective clinical study on the efficacy of collagenase clostridium histolyticum (CCH) injections in the thumb and first web space contractures in Dupuytren's Disease | ||
| Medical condition: Dupuytren's Disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-001656-22 | Sponsor Protocol Number: 1601 | Start Date*: 2016-11-17 | |||||||||||
| Sponsor Name:Ziekenhuis Oost Limburg | |||||||||||||
| Full Title: The utility of liposomal bupivacaine for anesthesia and analgesia in patients treated with collagenase for the release of Dupuytren’s contracture: A randomized controlled trial. | |||||||||||||
| Medical condition: Introduction of collagenase clostridium histolyticum injection for the treatment of Dupuytren’s contractures. | |||||||||||||
					
						
							
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-004251-76 | Sponsor Protocol Number: 87230 | Start Date*: 2017-05-22 | ||||||||||||||||
| Sponsor Name:University Hospitals of Leicester NHS Trust | ||||||||||||||||||
| Full Title: A pragmatic multi-centre randomised controlled non-inferiority, cost effectiveness trial comparing injections of collagenase into the cord to surgical correction in the treatment of moderate Dupuyt... | ||||||||||||||||||
| Medical condition: Dupuytren's contracture | ||||||||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2008-007872-99 | Sponsor Protocol Number: AUX-CC-860 | Start Date*: 2010-02-01 | |||||||||||
| Sponsor Name:Auxilium UK Limited | |||||||||||||
| Full Title: Long term follow up of subjects treated with AA4500 in studies AUX-CC-854, AUX-CC-856, AUX-CC-857/AUX-CC-858 and AUX-CC-859 | |||||||||||||
| Medical condition: Dupuytren's contracture | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) DK (Completed) SE (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-022921-13 | Sponsor Protocol Number: AUX-CC-802 | Start Date*: 2011-01-24 | |||||||||||
| Sponsor Name:Auxilium UK Limited | |||||||||||||
| Full Title: A PHASE 3, OPEN-LABEL STUDY OF THE SAFETY AND EFFECTIVENESS OF AA4500 ADMINISTERED TWICE PER TREATMENT CYCLE FOR UP TO FOUR TREATMENT CYCLES (2 x 4) IN MEN WITH PEYRONIE’S DISEASE | |||||||||||||
| Medical condition: Peyronie's Disease | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: SE (Completed) GB (Completed) DE (Completed) DK (Completed) FR (Completed) ES (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-004239-37 | Sponsor Protocol Number: AUX-CC-810 | Start Date*: 2015-02-26 | ||||||||||||||||
| Sponsor Name:Auxilium UK Limited | ||||||||||||||||||
| Full Title: Long-term safety, curvature deformity characterization, and immunogenicity over time in subjects previously treated with AA4500 for Peyronie’s disease in studies AUX-CC-802, AUX-CC-803, AUX CC 804,... | ||||||||||||||||||
| Medical condition: Peyronie's Disease | ||||||||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
| Trial protocol: SE (Completed) GB (Completed) DK (Completed) ES (Completed) IT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2012-005357-23 | Sponsor Protocol Number: 01 | Start Date*: 2013-01-27 | |||||||||||
| Sponsor Name:AUSL VITERBO | |||||||||||||
| Full Title: Preventing injection pain by Clostridium Histolyticum Collagenase Administration for teatment of Dupuytrens contracture | |||||||||||||
| Medical condition: Dupuytren s Disease | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-004649-28 | Sponsor Protocol Number: CTO-201 | Start Date*: 2015-10-09 | 
| Sponsor Name:Matrizyme Pharma Corporation | ||
| Full Title: A 2-stage study to evaluate single doses of MZ-004 at different dose levels in patients with chronic total occlusions. STAGE 1: Open label Training Stage. STAGE 2: Double-blind, randomized, Pla... | ||
| Medical condition: The use of MZ-004 to facilitate percutaneous coronary intervention in symptomatic patients with a chronic total occlusion who are indicated for revascularization | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-004091-19 | Sponsor Protocol Number: AUX-CC-867 | Start Date*: 2012-12-28 | |||||||||||
| Sponsor Name:Auxilium UK Limited | |||||||||||||
| Full Title: A Phase 3b open-label, historically-controlled study to assess the safety and efficacy of two concurrent injections of AA4500 in adult subjects with multiple Dupuytren’s contractures with palpable ... | |||||||||||||
| Medical condition: Dupuytren's contracture | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) GB (Completed) DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-001672-55 | Sponsor Protocol Number: MW2010-03-02 | Start Date*: 2014-09-22 | |||||||||||
| Sponsor Name:MediWound Ltd. | |||||||||||||
| Full Title: A multicenter, multinational, randomized, controlled, assessor blinded study, performed in subjects with thermal burns, to evaluate the efficacy and safety of NexoBrid compared to Gel Vehicle and c... | |||||||||||||
| Medical condition: The study objective is to evaluate the efficacy and safety of NexoBrid in removing burn eschar in hospitalized subjects with thermal burns. | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) CZ (Completed) RO (Completed) LV (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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