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