- Trials with a EudraCT protocol (248)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
		
	   		
	   		    
                    
                   	
                   	    248 result(s) found for: Meningococcal vaccine.
                    
                
			
   			
		
		Displaying page 1 of 13.
	
	
	| EudraCT Number: 2015-005189-48 | Sponsor Protocol Number: MPS01 | Start Date*: 2015-11-17 | 
| Sponsor Name:Sanofi Pasteur SA | ||
| Full Title: Safety and Immunogenicity of Sanofi Pasteur Meningococcal (Groups A and C) Polysaccharide Vaccine versus Lanzhou Institute of Biological Products Meningococcal (Groups A and C) Polysaccharide Vacci... | ||
| Medical condition: Meningococcal Disease | ||
| Disease: | ||
| Population Age: Children, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2025-000103-23 | Sponsor Protocol Number: MEQ00075 | Start Date*: 2025-04-09 | |||||||||||
| Sponsor Name:Sanofi Pasteur Inc. | |||||||||||||
| Full Title: Phase I Open-Label, Age De-escalation Safety and Immunogenicity Study of an Investigational Quadrivalent Meningococcal Conjugate Vaccine in Healthy Adolescents, Children, Toddlers, and Infants in C... | |||||||||||||
| Medical condition: Meningococcal infection | |||||||||||||
| 
 | |||||||||||||
| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-000104-38 | Sponsor Protocol Number: MEQ00073 | Start Date*: 2021-06-17 | |||||||||||
| Sponsor Name:Sanofi Pasteur | |||||||||||||
| Full Title: A Phase IIIb, Open-label, Multi-center Study to Evaluate the Immunogenicity and Safety of a Booster Dose and Describe the Immune Persistence of MenACYW Conjugate Vaccine with 5- and/or 10-year Boos... | |||||||||||||
| Medical condition: Meningococcal infection | |||||||||||||
| 
 | |||||||||||||
| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Trial now transitioned) HU (Trial now transitioned) DE (Trial now transitioned) ES (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-004731-36 | Sponsor Protocol Number: MET58 | Start Date*: 2018-09-27 | |||||||||||
| Sponsor Name:Sanofi Pasteur Inc. | |||||||||||||
| Full Title: Immunogenicity and Safety Study of an Investigational Quadrivalent Meningococcal Conjugate Vaccine when Administered Concomitantly with Routine Pediatric Vaccines in Healthy Infants and Toddlers in... | |||||||||||||
| Medical condition: Healthy volunteers (active immunization against invasive meningogoccal disease (IMD) caused by Meningococcal serogroups A, C, Y or W) | |||||||||||||
| 
 | |||||||||||||
| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) SE (Completed) FI (Completed) IT (Completed) ES (Completed) PL (Completed) RO (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-001471-20 | Sponsor Protocol Number: MET35 | Start Date*: 2018-07-10 | |||||||||||
| Sponsor Name:Sanofi Pasteur Inc. | |||||||||||||
| Full Title: Immunogenicity and Safety of an Investigational Quadrivalent Meningococcal Conjugate Vaccine Administered in Healthy Children 2 to 9 Years of Age | |||||||||||||
| Medical condition: Healthy volunteers (active immunization against invasive meningogoccal disease (IMD) caused by Meningococcal serogroups A, C, Y or W) | |||||||||||||
| 
 | |||||||||||||
| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-001349-17 | Sponsor Protocol Number: OVG2007/4 | Start Date*: 2009-04-27 | |||||||||||
| Sponsor Name:University of Oxford | |||||||||||||
| Full Title: A single centre, open-label, randomised clinical trial to investigate Meningococcal serogroup A, C, W-135 and Y saccharide specific B cell response to a primary and a booster dose of the Meningococ... | |||||||||||||
| Medical condition: The Novartis Meningococcal A, C, W-135 and Y vaccine is intended for prevention of meningitis and/or septicemia caused by Neisseria meningitidis serogroups A, C, W-135 and Y. | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-003504-79 | Sponsor Protocol Number: V59P13 | Start Date*: 2014-10-24 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:Novartis Vaccines & Diagnostics, Inc. | ||||||||||||||||||||||||||||||||||||||
| Full Title: A Phase 3, Randomized, Observer-blind, Controlled, Multi-Center Study to Evaluate the Lot to Lot Consistency of Investigational Meningococcal ACWY Conjugate Vaccine when One Dose is Administered t... | ||||||||||||||||||||||||||||||||||||||
| Medical condition: Novartis Meningococcal ACWY conjugate vaccine is intended for prevention of meningitis and septicemia caused by Neisseria meningitidis serogroups A, C, W and Y. | ||||||||||||||||||||||||||||||||||||||
| 
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: Outside EU/EEA | ||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2018-001470-18 | Sponsor Protocol Number: MET56 | Start Date*: 2018-07-10 | |||||||||||
| Sponsor Name:Sanofi Pasteur Inc. | |||||||||||||
| Full Title: Immunogenicity and Safety of a Booster Dose of an Investigational Quadrivalent Meningococcal Conjugate Vaccine | |||||||||||||
| Medical condition: Healthy adolescents and adults who had received 1 dose of a quadrivalent meningococcal conjugate vaccine 4 to 10 years previously | |||||||||||||
| 
 | |||||||||||||
| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-003694-29 | Sponsor Protocol Number: V72_37 | Start Date*: 2013-03-26 | |||||||||||
| Sponsor Name:NOVARTIS VACCINES AND DIAGNOSTICS S.R.L. | |||||||||||||
| Full Title: A Phase 3b, Multi-Center, Open-label Study to Assess the Safety of Novartis Meningococcal B Recombinant Vaccine When Administered at a 0, 2-Month Schedule in Healthy at-risk Adults | |||||||||||||
| Medical condition: Healthy volunteers (Meningitis B) | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-005641-21 | Sponsor Protocol Number: 112148 | Start Date*: 2015-05-26 | ||||||||||||||||
| Sponsor Name:GlaxoSmithKline Biologicals | ||||||||||||||||||
| Full Title: A phase III, open, controlled study to assess the persistence of antibodies after one dose of GlaxoSmithKline Biologicals’ meningococcal serogroup ACWY conjugate vaccine (MenACWY-TT) given intramus... | ||||||||||||||||||
| Medical condition: Prevention of invasive meningococcal disease caused by Neisseria meningitidis serogroups A, C, W and/or Y | ||||||||||||||||||
| 
 | ||||||||||||||||||
| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: Outside EU/EEA | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2012-002719-24 | Sponsor Protocol Number: 112021 | Start Date*: 2015-06-01 | ||||||||||||||||
| Sponsor Name:GlaxoSmithKline Biologicals | ||||||||||||||||||
| Full Title: A phase II, open, multi-center study to evaluate the long-term anti-body persistence at 1 year, 3 years and 5 years after the administration of one or two doses of GlaxoSmithKline (GSK) Biologicals... | ||||||||||||||||||
| Medical condition: Invasive disease caused by Neisseria meningitidis serogroups A, C W-135 and Y | ||||||||||||||||||
| 
 | ||||||||||||||||||
| Population Age: Children, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: Outside EU/EEA | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2019-004461-41 | Sponsor Protocol Number: MET59 | Start Date*: 2020-02-14 | |||||||||||
| Sponsor Name:Sanofi Pasteur Inc | |||||||||||||
| Full Title: Immunogenicity and Safety of a Booster Dose of an Investigational Quadrivalent Meningococcal Conjugate Vaccine in Adolescents and Adults | |||||||||||||
| Medical condition: Healthy volunteers (active immunization against invasive meningogoccal disease (IMD) caused by Meningococcal serogroups A, C, Y and W) | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2025-000002-42 | Sponsor Protocol Number: MEQ00086 | Start Date*: 2025-04-10 | |||||||||||
| Sponsor Name:Sanofi Pasteur | |||||||||||||
| Full Title: A descriptive, Phase IV, open-label, single-arm multi-center study to assess the immunogenicity and safety of MenQuadfi® as a booster vaccine in healthy toddlers 12 to 23 months of age who had been... | |||||||||||||
| Medical condition: Meningococcal infection | |||||||||||||
| 
 | |||||||||||||
| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-004341-36 | Sponsor Protocol Number: MET55 | Start Date*: 2020-12-04 | |||||||||||
| Sponsor Name:Sanofi Pasteur Inc | |||||||||||||
| Full Title: Immunogenicity and Safety of an Investigational Quadrivalent Meningococcal Conjugate Vaccine in Healthy Adults, Adolescents, and Children in India and Healthy Adolescents and Children in the Republ... | |||||||||||||
| Medical condition: Meningococcal infection | |||||||||||||
| 
 | |||||||||||||
| Population Age: Children, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-000048-28 | Sponsor Protocol Number: EC002(Quad1) - C59P1 | Start Date*: 2007-06-22 | ||||||||||||||||
| Sponsor Name:University Hospitals Bristol NHS Foundation Trust | ||||||||||||||||||
| Full Title: An open lable, randomised, controlled two centre study to evaluate the mucosal immune response to a quadrivalent meningococcal conjugate vaccine in healthy adults. | ||||||||||||||||||
| Medical condition: Prevention of meningococcal infection | ||||||||||||||||||
| 
 | ||||||||||||||||||
| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2016-000749-30 | Sponsor Protocol Number: MET51 | Start Date*: 2016-11-30 | |||||||||||
| Sponsor Name:Sanofi Pasteur | |||||||||||||
| Full Title: Immunogenicity and Safety of an Investigational Quadrivalent Meningococcal Conjugate Vaccine in Toddlers 12 to 23 Months of Age | |||||||||||||
| Medical condition: Healthy volunteers (active immunization against invasive meningogoccal disease (IMD) caused by Meningococcal serogroups A, C, Y or W) | |||||||||||||
| 
 | |||||||||||||
| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) FI (Completed) HU (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-002410-36 | Sponsor Protocol Number: 115524 | Start Date*: 2012-07-10 | |||||||||||
| Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||
| Full Title: A phase III, open, controlled study to evaluate immunogenicity of GSK Biologicals’ MenACWY-TT conjugate vaccine administered intramuscularly to at risk subjects from 1 to less than 18 years and to ... | |||||||||||||
| Medical condition: Meningococcal infection | |||||||||||||
| 
 | |||||||||||||
| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-000283-23 | Sponsor Protocol Number: 109495 | Start Date*: 2012-04-12 | |||||||||||
| Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||
| Full Title: A phase III, open, randomized, controlled primary vaccination study to demonstrate the non-inferiority of meningococcal vaccine GSK134612 given intramuscularly versus Mencevax™ ACWY given subcutane... | |||||||||||||
| Medical condition: Meningococcal disease | |||||||||||||
| 
 | |||||||||||||
| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-000282-20 | Sponsor Protocol Number: 109069 | Start Date*: 2012-04-12 | |||||||||||
| Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||
| Full Title: A phase III, randomized, open, controlled, multicenter primary vaccination study to demonstrate the non inferiority of the immunogenicity of meningococcal vaccine GSK134612 given intramuscularly ve... | |||||||||||||
| Medical condition: Meningococcal disease | |||||||||||||
| 
 | |||||||||||||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2023-000924-13 | Sponsor Protocol Number: VAN00010 | Start Date*: 2023-12-21 | |||||||||||
| Sponsor Name:Sanofi Pasteur Inc. | |||||||||||||
| Full Title: A Phase I/II, Randomized, Descriptive, Safety and Immunogenicity study to assess Pentavalent Meningococcal ABCYW Vaccine formulations in Adults (18 to 25 years of age) and Adolescents (10 to 17 yea... | |||||||||||||
| Medical condition: Bacterial infections and mycoses | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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