- Trials with a EudraCT protocol (39)
 - Paediatric studies in scope of Art45 of the Paediatric Regulation (10)
 
		
	   		
	   		    
                    
                   	
                   	    39 result(s) found for: Teenagers.
                    
                
			
   			
		
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	| EudraCT Number: 2017-003239-13 | Sponsor Protocol Number: PIMAT | Start Date*: 2017-10-02 | |||||||||||
| Sponsor Name:Imperial College London JRC Office | |||||||||||||
| Full Title: Pharmacokinetics of Intramuscular Adrenaline in Food-Allergic Teenagers - does dose matter? The PIMAT study | |||||||||||||
| Medical condition: Anaphylaxis | |||||||||||||
					
						
							
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| Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-002974-35 | Sponsor Protocol Number: Tonab101 | Start Date*: 2014-10-07 | 
| Sponsor Name:Umeå University | ||
| Full Title: Is home abortion mora acceptable for teenagers than abortion at the clinic? A randomized trial. | ||
| Medical condition: Young women with unwanted pregnancies seeking abortion care | ||
| Disease: | ||
| Population Age: Adolescents, Under 18 | Gender: Female | |
| Trial protocol: SE (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-004828-11 | Sponsor Protocol Number: RECHMPL18_0038_prom_7574 | Start Date*: 2022-01-10 | 
| Sponsor Name:University Hospital of Montpellier | ||
| Full Title: Phosphodiesterase-type 5 inhibitors in adult and adolescent patients with univentricular heart disease: a multi-center, randomized, double blind phase III study | ||
| Medical condition: adult and adolescent patients with univentricular heart diseases and pulmonary arterial pressure | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: FR (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-006558-17 | Sponsor Protocol Number: | Start Date*: 2010-01-21 | 
| Sponsor Name:cliniques universitaire de mont godinne | ||
| Full Title: | ||
| Medical condition: major depression | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-002193-23 | Sponsor Protocol Number: HLS04/2011 | Start Date*: 2011-09-27 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA L. SACCO (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
| Full Title: Long term Immunogenicity of Quadrivalent Human Papillomavirus vaccine (Gardasil) in HIV-infected adolescents and young adults vs. healthy adolescents and young adults: non-randomized controlled cli... | |||||||||||||
| Medical condition: HIV+ teenagers and young adults versus HIV-negative subjects: high-risk population for HPV-related disease. | |||||||||||||
					
						
							
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-001772-10 | Sponsor Protocol Number: 2016-06 | Start Date*: 2020-02-14 | |||||||||||
| Sponsor Name:Assistance Publique-Hôpitaux de Marseille | |||||||||||||
| Full Title: Phase I study of oral metronomic NAVELBINE® and HEMANGIOL®combination for children and teenagers with refractory/relapsing solid tumors | |||||||||||||
| Medical condition: Pediatric Solid tumor | |||||||||||||
					
						
							
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-005678-61 | Sponsor Protocol Number: ESNOD-01 | Start Date*: 2006-02-22 | 
| Sponsor Name:University Hospital Tuebingen | ||
| Full Title: Entwicklung einer Untersuchungsmethode zur Bestimmung des NO-Transferfaktors der Lunge Evaluierung der Methode und Normwerterhebung an gesunden Probanden (Development of a new method for steady-sta... | ||
| Medical condition: Lung function testing (NO- and CO Transferfactor) in healthy subjects | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-001298-96 | Sponsor Protocol Number: I6T-MC-AMBU | Start Date*: 2019-10-08 | |||||||||||
| Sponsor Name:Eli Lilly and Company Limited | |||||||||||||
| Full Title: Protocol I6T-MC-AMBU A Mulitcenter, Open-Label PK Study of Mirikizumab in Pediatric Patients with Moderately to Severely Active Ulcerative Colitis | |||||||||||||
| Medical condition: Moderately to severely active ulcerative colitis | |||||||||||||
					
						
							
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-004609-42 | Sponsor Protocol Number: OVG2017/08 | Start Date*: 2018-02-21 | ||||||||||||||||
| Sponsor Name:Clinical Trials and Research Governance (CTRG), University of Oxford | ||||||||||||||||||
| Full Title: Evaluating the effect of immunisation with group B meningococcal vaccines on meningococcal carriage | ||||||||||||||||||
| Medical condition: Oropharyngeal meningococcal carriage. Meningococci have the potential to cause invasive meningococcal disease. This study investigates the ability of Meningococcal B vaccines to reduce the carriage... | ||||||||||||||||||
					
						
							
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| Population Age: Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2018-002562-40 | Sponsor Protocol Number: 16-021 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Portola Pharma UK Ltd | |||||||||||||
| Full Title: A phase 1, open-label, single dose, non-randomized study to evaluate pharmacokinetics, pharmacodynamics, and safety of Betrixaban in pediatric patients. | |||||||||||||
| Medical condition: Pediatric patients who are assessed to be at risk for Venous thromboembolism (VTE) but does not require immediate anticoagulant therapy, for example: a. Has previous thrombosis and completed a cour... | |||||||||||||
					
						
							
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-004780-71 | Sponsor Protocol Number: PROFERTIL | Start Date*: Information not available in EudraCT | 
| Sponsor Name:Karolinska University Hospital | ||
| Full Title: A phase III Randomized Double-Blinded Placebo-Controlled Study of Use of GnRHa during Chemotherapy for Fertility Protection of Young Women and Teenagers with Cancer - ProFertil | ||
| Medical condition: Breast Cancer Acute Leukemia Lymphomas (Hodgkin and non-Hodgkin) Sarcomas (Osteo, Soft tissue and Ewing) | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults | Gender: Female | |
| Trial protocol: SE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-001286-16 | Sponsor Protocol Number: APP-study | Start Date*: 2018-11-05 | |||||||||||
| Sponsor Name:Rigshospitalet | |||||||||||||
| Full Title: Low-dose Atropine for the Prevention of Childhood Myopia Progression in Danish Children (APP-study) | |||||||||||||
| Medical condition: Childhood myopia | |||||||||||||
					
						
							
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-000096-32 | Sponsor Protocol Number: METRO-PD1-1708 | Start Date*: 2018-11-15 | ||||||||||||||||||||||||||
| Sponsor Name:Centre Oscar Lambret | ||||||||||||||||||||||||||||
| Full Title: Metro-PD1: a phase I/II trial evaluating anti-PD1 (Nivolumab) in combination with metronomic chemotherapy in children and teenagers with refractory /relapsing solid tumors or lymphoma | ||||||||||||||||||||||||||||
| Medical condition: Progressive or refractory : • high grade glioma • neuroblastoma • other cerebral tumors • lymphoma | ||||||||||||||||||||||||||||
					
						
							
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: FR (Trial now transitioned) BE (Prematurely Ended) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2018-003845-40 | Sponsor Protocol Number: 122-0551-209 | Start Date*: 2019-07-09 | |||||||||||
| Sponsor Name:Mayne Pharma LLC | |||||||||||||
| Full Title: An open label evaluation of the adrenal suppression potential and pharmacokinetic properties of twice daily halobetasol propionate foam, 0.05% in subjects 12 to less than 18 years of age with plaqu... | |||||||||||||
| Medical condition: Plaque psoriasis | |||||||||||||
					
						
							
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| Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-002122-23 | Sponsor Protocol Number: NL44307.078.13 | Start Date*: 2013-07-11 | 
| Sponsor Name:Erasmus University Medical Center | ||
| Full Title: The influence of electroencephalographic Narcotrend Index™- guidance of of propofol administration on recovery from procedural sedation for gastrointestinal endoscopy in paediatric patients | ||
| Medical condition: There is no medical condition which is under investigation. Paediatric patients, scheduled for gastrointestinal endoscopy under procedural sedation are eligible for inclusion. Depth of sedation wil... | ||
| Disease: | ||
| Population Age: Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-004468-22 | Sponsor Protocol Number: HEAD-STUDIE | Start Date*: 2006-03-31 | 
| Sponsor Name:Klinikum der Universität München, Kinderklinik und Poliklinik im Dr. von Haunerschen Kinderspital | ||
| Full Title: HEAD-TO-HEAD evaluation of the antiepileptic drugs Levetiracetam (LEV) vs. Sulthiame (STM) in a German multi-centre, doubleblind controlled trial in children with benign epilepsy with centro-tempor... | ||
| Medical condition: Benign epilepsy of childhood with centro-temporal spikes (BECTS) | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-001927-74 | Sponsor Protocol Number: SysVac01-C60P2 (PA/2008/2883) | Start Date*: 2009-01-16 | 
| Sponsor Name:University Hospitals Bristol NHS Foundation Trust | ||
| Full Title: A PHASE II, OPEN LABEL, RANDOMISED, TWO CENTRE STUDY TO EVALUATE THE IMPORTANCE OF NATURALLY INDUCED IMMUNE REGULATION ON THE MUCOSAL IMMUNE RESPONSE TO MENINGOCOCCAL SEROGROUP B OUTER MEMBRANE VES... | ||
| Medical condition: "Healthy volunteers" In this project we will establish whether naturally induced mucosal CD25+ T regulatory activity in adults and adolescents modulates the mucosal immune response to systemic Me... | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-004732-11 | Sponsor Protocol Number: | Start Date*: 2018-01-19 | 
| Sponsor Name:University of Oxford | ||
| Full Title: Preventing meningitis in young people after infant immunisation: effect of a single meningococcal 4CMenB vaccine booster over 10 years of age | ||
| Medical condition: Meningococcus group B disease, which can cause a variety of symptoms. The most serious of these are meningitis, and septicaemia (also known as blood poisoning). | ||
| Disease: | ||
| Population Age: Children, Under 18 | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-000081-11 | Sponsor Protocol Number: BFS-AS-306 | Start Date*: 2013-05-28 | |||||||||||
| Sponsor Name:Teva Branded Pharmaceutical Products R&D, Inc. | |||||||||||||
| Full Title: A 12-Week Efficacy and Safety Evaluation of Budesonide/Formoterol SPIROMAX® 160/4.5 mcg Inhalation Powder Versus SYMBICORT® TURBOHALER® 200/6 mcg in Adult and Adolescent Patients with Persistent As... | |||||||||||||
| Medical condition: Persistent Asthma | |||||||||||||
					
						
							
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) AT (Completed) DE (Completed) BE (Completed) IT (Completed) SE (Completed) CZ (Completed) FI (Completed) ES (Completed) PL (Completed) NL (Completed) DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-001696-30 | Sponsor Protocol Number: TMC278-TiDP38-C213 | Start Date*: 2009-01-21 | |||||||||||
| Sponsor Name:Tibotec Pharmaceuticals Ltd. | |||||||||||||
| Full Title: Ensayo fase II, abierto, de un solo brazo de tratamiento para evaluar la farmacocinética, seguridad, tolerabilidad y actividad antiviral de TMC278 en pacientes adolescentes de entre 12 y 18 años de... | |||||||||||||
| Medical condition: HIV-1 Infection | |||||||||||||
					
						
							
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| Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
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