- Trials with a EudraCT protocol (154)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
154 result(s) found for: Influenza Vaccines AND Influenza Virus.
Displaying page 1 of 8.
EudraCT Number: 2008-001079-31 | Sponsor Protocol Number: V71P7S | Start Date*: 2008-04-22 | ||||||||||||||||||||||||||
Sponsor Name:NOVARTIS VACCINES AND DIAGNOSTICS S.R.L. | ||||||||||||||||||||||||||||
Full Title: A Phase II, Open Label, Uncontrolled, Multi Center Study to Evaluate Safety and Immunogenicity of AGRIPPAL S1 Surface Antigen, Inactivated, Influenza Vaccine, Formulation 2008-2009, when Administer... | ||||||||||||||||||||||||||||
Medical condition: Prophylaxis against flu virus 2008-2009. | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-002871-15 | Sponsor Protocol Number: V58P13 | Start Date*: 2007-09-14 |
Sponsor Name:Novartis Vaccines and Diagnostics S.r.l. | ||
Full Title: A Phase III, Randomized, Observer-Blind, Placebo-Controlled, Multicenter Study to Assess Clinical Efficacy of a Cell-Derived Subunit Influenza Vaccine and an Egg-Derived Subunit Influenza Vaccine i... | ||
Medical condition: Influenza disease. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-018603-29 | Sponsor Protocol Number: V70_25S | Start Date*: 2010-05-17 | |||||||||||
Sponsor Name:NOVARTIS VACCINES AND DIAGNOSTICS S.R.L. | |||||||||||||
Full Title: A Phase II, Open Label, Uncontrolled, Multi Center Study to Evaluate Safety and Immunogenicity of FLUAD Surface Antigen, Inactivated, Adjuvanted with MF59C.1 Influenza Vaccine, Formulation 2010-201... | |||||||||||||
Medical condition: Influenza poses a significant threat to individual and public health, and influenza vaccination with a trivalent inactivated influenza vaccine is widely recommended to children, adults at risks and... | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-014719-11 | Sponsor Protocol Number: 2009/08 H1N1 | Start Date*: 2009-09-18 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:University of Oxford | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Open Label, Randomized, Parallel-Group, Multi-Center Study to Evaluate the Safety, Tolerability and Immunogenicity of Baxter H1N1 vaccine and GlaxoSmithKline H1N1 vaccine in children 6 months to 12... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Prophylaxis of influenza in an officially declared pandemic situation. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-021033-30 | Sponsor Protocol Number: H1N1-495-10THL | Start Date*: 2010-09-14 | |||||||||||
Sponsor Name:National Institute for Health and Welfare | |||||||||||||
Full Title: Evaluation of the effectiveness of vaccination with 2009 H1N1 vaccines during influenza season 2010-11 2009 H1N1-influenssarokotteiden tehokkuus influenssakaudella 2010-11 | |||||||||||||
Medical condition: Influenza caused by the 2009 H1N1 influenza virus ("swine influenza") | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000585-13 | Sponsor Protocol Number: MI-CP111 | Start Date*: 2004-09-01 | |||||||||||
Sponsor Name:MedImmune Vaccines, Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind Trial to Assess the Safety and Relative Efficacy of CAIV-T Against Inactivated Influenza Vaccine in Children 6–59 Months of Age | |||||||||||||
Medical condition: Influenza | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) SE (Completed) CZ (Completed) ES (Completed) IS (Completed) GB (Completed) IT (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002080-26 | Sponsor Protocol Number: V58P15 | Start Date*: 2013-08-28 | |||||||||||
Sponsor Name:Novartis Vaccines & Diagnostics AG | |||||||||||||
Full Title: A Phase III, Observer-Blind, Randomized Multicenter Study to Evaluate the Safety of Trivalent Subunit Influenza Vaccines, Produced Either in Mammalian Cell Culture (tivc) or in Embryonated Eggs (TI... | |||||||||||||
Medical condition: volunteers at high risk for influenza-related complications (protection against influenza) | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002781-12 | Sponsor Protocol Number: 2019061567 | Start Date*: 2021-08-05 | ||||||||||||||||
Sponsor Name:University of Southern Denmark, Bandim Health Project | ||||||||||||||||||
Full Title: Using BCG vaccine to strengthen the immune system in the elderly and improve the response to influenza vaccine. A randomized clinical trial. | ||||||||||||||||||
Medical condition: Immune response to seasonal influenza vaccine | ||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-003786-41 | Sponsor Protocol Number: V70P5 | Start Date*: 2007-10-22 |
Sponsor Name:Novartis Vaccines and Diagnostics S.r.l. | ||
Full Title: A Phase III, randomized, observer-blind, controlled, multi-center clinical study to evaluate the efficacy, safety and immunogenicity of one and two intramuscular doses of FLUAD versus control vacci... | ||
Medical condition: no medical, condition: healthy, | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) FI (Completed) IT (Completed) HU (Completed) BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-003170-31 | Sponsor Protocol Number: QHD00027 | Start Date*: 2021-08-16 | |||||||||||
Sponsor Name:Cardiovascular Non-Invasive Imaging Research Laboratory, Department of Cardiology, Herlev and Gentofte Hospital | |||||||||||||
Full Title: Feasibility of Randomizing Danish Citizens Aged 65-79 Years to High-Dose Quadrivalent Influenza Vaccine vs. Standard-Dose Quadrivalent Influenza Vaccine in a Pragmatic Registry-Based Setting | |||||||||||||
Medical condition: Prevention of influenza infection in adults aged 65-79 years | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011450-18 | Sponsor Protocol Number: CSLCT-NHF-09-57 | Start Date*: 2009-04-24 | |||||||||||
Sponsor Name:CSL Limited | |||||||||||||
Full Title: A Phase IV, Single-centre, Open-label Study to Evaluate the Immunogenicity and Safety of the 2009/2010 Formulation of the Enzira® Vaccine in Two Groups of Healthy Volunteers: ‘Adults’ (aged ≥ 18 to... | |||||||||||||
Medical condition: Prophylaxis of influenza | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005558-63 | Sponsor Protocol Number: V70P3 | Start Date*: 2006-11-28 | |||||||||||
Sponsor Name:Novartis Vaccines and Diagnostics S.r.l. | |||||||||||||
Full Title: A phase III, randomized, controlled, observer-blind, single-center study to compare immunogenicity and safety of an MF59-adjuvanted inactivated subunit influenza vaccine (FLUAD™) to those of a nona... | |||||||||||||
Medical condition: Influenza | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003953-43 | Sponsor Protocol Number: VAC31518COV3005 | Start Date*: 2021-11-29 | ||||||||||||||||
Sponsor Name:Janssen Vaccines & Prevention B.V. | ||||||||||||||||||
Full Title: A Randomized, Double-blind, Phase 3 Study to Evaluate Safety, Reactogenicity, and Immunogenicity of Co-administration of Ad26.COV2.S and Influenza Vaccines in Healthy Adults 18 Years of Age and Older | ||||||||||||||||||
Medical condition: Healthy Volunteers (Prevention of COVID-19 and influenza) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: PL (Completed) BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-003166-32 | Sponsor Protocol Number: FLUVALAB-H-14 | Start Date*: 2011-08-30 | |||||||||||
Sponsor Name:Omninvest Ltd. | |||||||||||||
Full Title: A Randomized, Double-blind, Multi-Center Study to Evaluate Safety and Immunogenicity of One Dose of Four FLUVAL AB-like (Trivalent, Whole Virus, Aluminium Phosphate Gel Adjuvanted) Influenza Vaccin... | |||||||||||||
Medical condition: Immunization of healthy people against influenza virus infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003339-22 | Sponsor Protocol Number: V70P2E1 | Start Date*: 2007-10-11 |
Sponsor Name:Novartis Vaccines and Diagnostics S.r.l. | ||
Full Title: A Phase II, Observer-Blind, Parallel Groups, Single-Center, Extension Study to Evaluate the Immunogenicity and Safety Following a Single Intramuscular Dose of FLUAD or Vaxigrip Influenza Vaccines i... | ||
Medical condition: Influenza | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-004904-74 | Sponsor Protocol Number: INFQ3003 | Start Date*: 2017-09-07 | |||||||||||
Sponsor Name:Abbott Biologicals B.V. | |||||||||||||
Full Title: A Phase III, Observer-Blind, Randomized, Non-influenza Vaccine Comparator-Controlled, Parallel-Group, Multi-Country Study in Children Aged 6-35 Months to Assess the Safety and Efficacy of Abbott’s ... | |||||||||||||
Medical condition: Prophylaxis of Influenza | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) DK (Completed) EE (Ongoing) CZ (Completed) LT (Completed) BG (Completed) IT (Completed) SI (Completed) ES (Completed) FR (Not Authorised) HR (Completed) HU (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-014770-17 | Sponsor Protocol Number: NVI-255 | Start Date*: 2009-10-09 |
Sponsor Name:Netherlands Vaccine Institute | ||
Full Title: New influenza A (H1N1) disease incidence and immunogenicity of the pandemic influenza A (H1N1) vaccine in healthy adults | ||
Medical condition: influenza A (H1N1) virus infection | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-001032-57 | Sponsor Protocol Number: M13-567 | Start Date*: 2012-06-26 | |||||||||||
Sponsor Name:Abbott Biologicals B.V. | |||||||||||||
Full Title: Immunogenicity, Reactogenicity and Safety of the Trivalent Influenza Subunit Vaccine Influvac® for the Northern Hemisphere Season 2012/2013. An Open-Label, Baseline- Controlled Study in Two Age ... | |||||||||||||
Medical condition: Prophylaxis of Influenza | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021644-18 | Sponsor Protocol Number: V70P5E1 | Start Date*: 2010-09-17 | |||||||||||
Sponsor Name:Novartis Vaccines and Diagnostics S.r.l. | |||||||||||||
Full Title: A Phase IIIB, observer-blind, randomized, parallel groups, extension study to evaluate the immunogenicity and safety following a single intramuscular dose of FLUAD or Agrippal S1 influenza vaccines... | |||||||||||||
Medical condition: Influenza | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000881-12 | Sponsor Protocol Number: M13-998 | Start Date*: 2013-07-11 | |||||||||||
Sponsor Name:Abbott Biologicals B.V | |||||||||||||
Full Title: Immunogenicity, Reactogenicity and Safety of the Trivalent Influenza Subunit Vaccine Influvac® for the Northern Hemisphere Season 2013/2014. An Open-Label, Baseline- Controlled Study in Two Age Gro... | |||||||||||||
Medical condition: Prophylaxis of Influenza | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
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