- Trials with a EudraCT protocol (227)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
		
	   		
	   		    
                    
                   	
                   	    227 result(s) found for: eudract.
                    
                
			
   			
		
		Displaying page 1 of 12.
	
	
	| EudraCT Number: 2012-002053-29 | Sponsor Protocol Number: 03042012 | Start Date*: 2012-08-10 | |||||||||||
| Sponsor Name:Karolinska Institutet and University Hospital | |||||||||||||
| Full Title: PET/CT-biopsi study A PET/CT biopsy sub study in patients who have given informed consent to participate in a randomized, dubbel blind, placebo controlled phase III trial with Capecitabine +/- So... | |||||||||||||
| Medical condition: Morphological verifications of metastatic lesions, PET Ribonucleic Acid (RNA)-expression study in subjects with locally advance or metastatic HER2-negative breast cancer. | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: SE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-002422-29 | Sponsor Protocol Number: 1235.8 | Start Date*: 2007-10-19 | |||||||||||
| Sponsor Name:Boehringer Ingelheim Ltd. | |||||||||||||
| Full Title: An open-label follow-up trial of the efficacy and safety of chronic administration of the combination of telmisartan 40mg + amlodipine 10mg or the combination of telmisartan 80mg + amlodipine 10mg ... | |||||||||||||
| Medical condition: essential hypertension | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IE (Completed) GB (Completed) AT (Completed) CZ (Completed) ES (Completed) IT (Completed) BG (Completed) SK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-003293-93 | Sponsor Protocol Number: 14072011 | Start Date*: 2011-09-23 | 
| Sponsor Name:Sint Antonius Ziekenhuis | ||
| Full Title: Cyp3A4 metabolism before and after surgery induced weight loss in morbidly obese patients, using midazolam as a model drug | ||
| Medical condition: Morbid obesity | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-003512-37 | Sponsor Protocol Number: OC-AP-ICG-IV-2 | Start Date*: 2014-10-13 | 
| Sponsor Name:Jules Bordet Institute | ||
| Full Title: Study of the (intravenously injected) ICG (Indocyanine Green) imaging of tumoral implants in patients with peritoneal carcinomatosis from colorectal origin. | ||
| Medical condition: Imaging of tumours and their metastasis after intravenous injection of Indocyanine Green to patients with peritoneal carcinomatosis from colorectal cancer. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-003950-15 | Sponsor Protocol Number: rhLAMAN-10 | Start Date*: 2015-01-22 | |||||||||||
| Sponsor Name:Zymenex A/S | |||||||||||||
| Full Title: A single center, open label clinical trial investigating the long-term efficacy of rhLAMAN (recombinant human alpha-mannosidase or Lamazym) treatment in subjects with alpha-Mannosidosis who previo... | |||||||||||||
| Medical condition: alpha-Mannosidosis | |||||||||||||
| 
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-014816-37 | Sponsor Protocol Number: codice EUDRACT 2009-014816-37 | Start Date*: 2009-10-27 | 
| Sponsor Name:NAMED SRL | ||
| Full Title: Open prospective, uncontrolled pilot study to assess the tolerability and efficacy of Lymdiaral injektopas (Pascoe-Named) in the treatment of pannicolopatia-edema-fibrosclerotic (PEFS) and venous... | ||
| Medical condition: tolerability and efficacy of Lymdiaral Injektopas (Pascoe-Named) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: IT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-004253-10 | Sponsor Protocol Number: HI001 | Start Date*: 2006-05-19 | 
| Sponsor Name:Helena Isoniemi | ||
| Full Title: viite: EudraCT-numero 2005-004253-10 Tyypin 2 diabetesta sairastavien maksansiirtopotilaiden rasvamaksan hoito insuliiniherkistäjällä (rosiglitatsoni) | ||
| Medical condition: Maksansiirtopotilaat, joilla on todettu vaikea rasvamaksa (maksan rasvapitoisuus yli 50%) ja joilla on tyypin 2 diabetes. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-000404-28 | Sponsor Protocol Number: CRAD001ANO05 | Start Date*: 2016-07-20 | |||||||||||
| Sponsor Name:Novartis Norge AS | |||||||||||||
| Full Title: 5, 6 or 7 year follow-up control after the SCHEDULE study (SCANDINAVIAN HEART TRANSPLANT EVEROLIMUS DE NOVO STUDY WITH EARLY CNI AVOIDANCE) Title of the original SCHEDULE study: A controlled ran... | |||||||||||||
| Medical condition: Heart transplantation | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-004355-40 | Sponsor Protocol Number: rhLAMAN-04 | Start Date*: 2012-01-17 | 
| Sponsor Name:Zymenex A/S | ||
| Full Title: A multi-center, open-label trial of the long-term efficacy and safety of Lamazym for the treatment of patients with alpha-Mannosidosis. | ||
| Medical condition: Treatement of Alpha-Mannosidosis | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: DK (Completed) DE (Completed) BE (Completed) GB (Completed) ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-003399-37 | Sponsor Protocol Number: C0524T18 | Start Date*: 2007-11-27 | |||||||||||
| Sponsor Name:Janssen Biologics B.V. | |||||||||||||
| Full Title: A Phase 3 Multicenter, Randomized, Placebo-controlled, Double blind Study to Evaluate the Safety and Efficacy of Golimumab Maintenance Therapy, Administered Subcutaneously, in Subjects with Moderat... | |||||||||||||
| Medical condition: Ulcerative Colitis (UC) | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) HU (Completed) AT (Completed) BE (Completed) FR (Completed) LT (Completed) LV (Prematurely Ended) NL (Completed) DK (Completed) SE (Completed) BG (Completed) SK (Completed) CZ (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-002281-31 | Sponsor Protocol Number: Piromelatine-IOP1 | Start Date*: 2016-09-19 | 
| Sponsor Name:Neurim Pharmaceuticals (1991) Ltd. | ||
| Full Title: A randomized, double-blind, placebo-controlled, study of oral treatment of piromelatine in patients with ocular hypertension (OHT) or primary open angle glaucoma (POAG). | ||
| Medical condition: ocular hypertension primary open angle glaucoma | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-004837-34 | Sponsor Protocol Number: STH17245 | Start Date*: 2014-08-20 | |||||||||||
| Sponsor Name:Sheffield Teaching Hospitals NHS Foundation Trust | |||||||||||||
| Full Title: Lung HeXeRT: Advanced proton, hyperpolarised 3helium and 129xenon magnetic resonance imaging for lung cancer radiotherapy planning and evaluation | |||||||||||||
| Medical condition: Lung Cancer | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-003199-10 | Sponsor Protocol Number: OLE-NLRC4/XIAP.2016.001 | Start Date*: Information not available in EudraCT | 
| Sponsor Name:AB2 Bio Ltd. | ||
| Full Title: Open-label extension study with Tadekinig alfa (r-hIL-18BP) to monitor safety and tolerability in patients with IL-18 driven monogenic autoinflammatory conditions: NLRC4 mutation and XIAP deficiency | ||
| Medical condition: NLRC4 mutation XIAP deficiency | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-002062-40 | Sponsor Protocol Number: UMCN-AKF-21.04 | Start Date*: 2021-11-29 | 
| Sponsor Name:Radboud university medical center | ||
| Full Title: Pharmacokinetic study with a loading dose of clofazimine in adult patients with nontuberculous mycobacterial disease | ||
| Medical condition: Nontuberculous mycobacterial disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-004396-35 | Sponsor Protocol Number: 06078SE-A | Start Date*: 2006-10-25 | 
| Sponsor Name:Belfast City Hospital Trust | ||
| Full Title: Investigation of the anti-inflammatory effects of simvastatin in a model of acute lung injury after inhalation of lipopolysaccharide by healthy volunteers | ||
| Medical condition: Acute lung injury (ALI) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-000324-19 | Sponsor Protocol Number: DDDCF14 | Start Date*: 2014-09-18 | 
| Sponsor Name:KU Leuven - Drug Delivery & Disposition | ||
| Full Title: Collection and characterization of gastrointestinal fluids in different populations and conditions | ||
| Medical condition: healthy human volunteers (administration of a proton-pump inhibitor) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-004340-37 | Sponsor Protocol Number: HX575-305 | Start Date*: 2008-11-11 | |||||||||||
| Sponsor Name:Hexal Biotech ForschungsGmbH | |||||||||||||
| Full Title: An open label, multinational, multicenter study to evaluate the safety of HX575 recombinant human erythropoietin alfa | |||||||||||||
| Medical condition: Subjects with chronic kidney disease (CKD) previously enrolled in other efficacy and/or safety studies with HX575, after these subjects have participated in the earlier study. | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SK (Prematurely Ended) DE (Completed) ES (Completed) BE (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-003398-28 | Sponsor Protocol Number: C0524T17 | Start Date*: 2007-11-15 | |||||||||||
| Sponsor Name:Centocor BV | |||||||||||||
| Full Title: A Phase 2/3 Multicenter, Randomized, Placebo-controlled, Double blind Study to Evaluate the Safety and Efficacy of Golimumab Induction Therapy, Administered Subcutaneously, in Subjects with Moderat... | |||||||||||||
| Medical condition: Ulcerative Colitis (UC) | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) HU (Completed) AT (Completed) BE (Completed) FR (Completed) LT (Completed) LV (Completed) NL (Completed) DK (Completed) SE (Completed) BG (Completed) SK (Completed) CZ (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-004478-24 | Sponsor Protocol Number: OV101-18-002 | Start Date*: 2020-06-05 | |||||||||||
| Sponsor Name:Ovid Therapeutics Inc. | |||||||||||||
| Full Title: An Open-Label Study to Evaluate the Long-Term Safety, Tolerability, and Efficacy of OV101 in Individuals with Angelman Syndrome (ELARA) | |||||||||||||
| Medical condition: Angelman Syndrome | |||||||||||||
| 
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-001905-93 | Sponsor Protocol Number: EGF102580 | Start Date*: 2005-07-11 | 
| Sponsor Name:GlaxoSmithKline R&D Ltd | ||
| Full Title: A Phase II study to evaluate the efficacy, safety and pharmacodynamics of lapatinib in combination with paclitaxel as neoadjuvant therapy in patients with newly diagnosed inflammatory breast cancer | ||
| Medical condition: Newly diagnosed infammatory breast cancer (IBC) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) ES (Completed) | ||
| Trial results: View results | ||
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