Recent Phase II vaccine trials
Below is a list of phase II trials performed since 2011, for trials conducted before, contact: cev@uantwerpen.be
			
					
			A Phase 2, Long-Term Immunogenicity Follow-up Trial of Adult and Elderly Subjects who have Previously Received an Intramuscular Injection of Norovirus GI.1/GII.4 Bivalent Virus-Like Particle Vaccine
			
														
					
	
	
			- EudraCT number: 2016-004288-37
 - ClinicalTrials.gov Identifier: NCT03039790
 - Sponsor protocol number: NOR-213
 - Phase: II
 - Population age: adults, elderly
 - Gender: male, female
 - Starting year @CEV: 2017
 
			
					
			Immunogenicity and safety of HBAI20 Hepatitis B vaccine in non-responders
			
														
					
	
	
			- EudraCT number:2016-002720-91
 - Sponsor protocol number: HBnr02
 - Phase: II
 - Population age: adults
 - Gender: male, female
 - Starting year @CEV: 2017
 
			
					
			A study to evaluate the reactogenicity, safety and immunogenicity of GlaxoSmithKline (GSK) Biologicals' investigational supra-seasonal universal influenza vaccines - inactivated (SUIVs) (GSK3816302A) in healthy adults aged 18 to 39 years
			
														
					
	
	
			- EudraCT number:2017-001584-20
 - Sponsor protocol number: 207543
 - Centre code: Flu-D-Suiv-001
 - Phase: II
 - Population age: adults (18 to 39y)
 - Gender: male, female
 - Starting year @CEV: 2017
 
			
					
			Safety and reactogenicity study of GlaxoSmithKline (GSK) Biologicals' investigational respiratory syncytial virus (RSV) vaccine (GSK3003891A) in healthy women
			
														
					
	
	
			- EudraCT number: 2015-005742-58
 - ClinicalTrials.gov Identifier: NCT02753413
 - Sponsor protocol number: 204813
 - Centre code: RSV-F-024
 - Phase: II
 - Population age: adults (18 to 45y, non-pregnant)
 - Gender: female
 - Starting year @CEV: 2016
 
			
					
			Safety and Immunogenicity of the Liquid Formulation of Group B Streptococcus Trivalent Vaccine and of the Lyophilized Formulation of Group B Streptococcus Trivalent Vaccine
			
														
					
	
	
			- EudraCT number: 2013-003111-22
 - ClinicalTrials.gov Identifier: NCT02270944
 - Sponsor protocol number: V98_21
 - Centre code: GBS_V98_21
 - Phase: II
 - Population age: adults (18 to 40y)
 - Gender: female
 - Starting year @CEV: 2015
 
			
					
			Phase II study of HPV vaccine in HPV infected women with normal cytology/ASCUS/LSIL
			
														
					
	
	
			- EudraCT number:2013-003358-25
 - ClinicalTrials.gov Identifier: NCT01957878
 - Sponsor protocol number: PC10VAC02
 - Centre code:
 - Phase: II
 - Population age: adults (25 to 50y)
 - Gender: female
 - Starting year @CEV: 2013
 
			
					
			Safety and Immunogenicity of Norovirus GI.1/GII.4 Bivalent VLP Vaccine
			
														
					
	
	
			- EudraCT number: 2013-001419-64
 - ClinicalTrials.gov Identifier: NCT02038907
 - Sponsor protocol number: Nor-107
 - Centre code:
 - Phase: II
 - Population age: adults (18 to 64y)
 - Gender: male, female
 - Starting year @CEV: 2013
 
			
					
			A Phase 2, open-label, single-center, extension study to evaluate the booster response induced by Vi-CRM197 after priming with either Vi-CRM197 or Typherix administered in adult subjects in H01_04TP study
			
														
					
	
	
			- EudraCT number: 2011-001448-31
 - Sponsor protocol number: H01_01E1TP (=EXT H01_01TP)
 - Centre code:
 - Phase: II
 - Population age: adults (18 to 40y)
 - Gender: male,female
 - Starting year @CEV: 2011