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