- Trials with a EudraCT protocol (64)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
64 result(s) found for: Flu season.
Displaying page 1 of 4.
EudraCT Number: 2009-017781-23 | Sponsor Protocol Number: 720903 | Start Date*: 2010-01-18 | |||||||||||
Sponsor Name:Baxter Innovations GmbH | |||||||||||||
Full Title: An Open Label Phase 3 Study to Assess the Safety and Immunogenicity of a Vero Cell-Derived Trivalent Seasonal Influenza Vaccine, Strain Composition 2009/2010, in an Adult Population | |||||||||||||
Medical condition: To verify the safety and immunogenicity of a trivalent seasonal influenza vaccine with strain composition according to WHO/EU recommendation for the 2009/2010 season, manufactured according to the ... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020026-17 | Sponsor Protocol Number: 721001 | Start Date*: 2010-08-23 | |||||||||||
Sponsor Name:Baxter Innovations GmbH | |||||||||||||
Full Title: AN OPEN-LABEL PHASE 3 STUDY TO ASSESS THE IMMUNOGENICITY AND SAFETY OF A VERO CELL-DERIVED TRIVALENT SEASONAL INFLUENZA VACCINE, STRAIN COMPOSITION 2010/2011, IN AN ADULT AND ELDERLY POPULATION | |||||||||||||
Medical condition: To verify the immunogenicity and tolerance of a trivalent seasonal influenza vaccine with strain composition according to WHO/EU recommendation for the 2010/2011 season for yearly licensing applica... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003250-41 | Sponsor Protocol Number: 1 | Start Date*: 2015-09-15 | |||||||||||
Sponsor Name:Public Health England | |||||||||||||
Full Title: Protection induced by Live Attenuated Influenza Vaccine (LAIV or Fluenz Tetra) - applied epidemiological study | |||||||||||||
Medical condition: There is no medical condition associated with this trial. The trial involves vaccination of healthy children with a licensed product according to the SmPC. The vaccination is Fluenz Tetra, a live... | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011283-11 | Sponsor Protocol Number: 720901 | Start Date*: 2009-05-06 | |||||||||||
Sponsor Name:Baxter Innovations GmbH | |||||||||||||
Full Title: AN OPEN-LABEL PHASE 3 STUDY TO ASSESS THE IMMUNOGENICITY AND SAFETY OF A VERO CELL-DERIVED TRIVALENT SEASONAL INFLUENZA VACCINE, STRAIN COMPOSITION 2009/2010, IN AN ADULT AND ELDERLY POPULATION | |||||||||||||
Medical condition: Propyhlaxis of Influenza infection To verify the immunogenicity and tolerance of a trivalent seasonal influenza vaccine with strain composition according to WHO/EU recommendation for the 2009/2010 ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019372-72 | Sponsor Protocol Number: MV22970 | Start Date*: 2010-04-16 | |||||||||||
Sponsor Name:Pharmahungary Group | |||||||||||||
Full Title: An Observational Study on the Pharmacokinetics of Oseltamivir in the Treatment of Influenza during Lactation. | |||||||||||||
Medical condition: Lactating women who present with clinical symptoms indicative of influenza will be recruited to receive immediate treatment with oseltamivir at a standard dose of 75 mg twice daily. These subjects ... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014765-74 | Sponsor Protocol Number: Fluval P-H-08 | Start Date*: 2009-08-13 | |||||||||||
Sponsor Name:Omninvest Ltd. | |||||||||||||
Full Title: Tolerability and Safety Study of Fluval P Monovalent Influenza Vaccine in Children | |||||||||||||
Medical condition: Immunization of children against infection caused by pandemic influenza (H1N1)09 virus. | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000872-25 | Sponsor Protocol Number: 106372 | Start Date*: 2008-08-26 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A randomized, observer-blind, active-controlled phase III study to demonstrate the superior efficacy of GSK Biologicals’ adjuvanted influenza candidate vaccine [GSK2186877A], administered intramusc... | ||
Medical condition: Immunization against influenza in male and female subjects aged 65 years or older. | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) NL (Completed) EE (Completed) FR (Completed) GB (Completed) CZ (Completed) BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-002147-10 | Sponsor Protocol Number: FLU-MARK | Start Date*: 2011-09-21 | ||||||||||||||||
Sponsor Name:Institute for Biomedical Aging Research | ||||||||||||||||||
Full Title: Influenza vaccination in old age: Immunological and biogerontological characterization of responders and non-responders | ||||||||||||||||||
Medical condition: This study will analyze cellular and humoral immune responses after seasonal vaccination against influenza. Healthy adults are vaccinated with a licensed trivalent inactivated vaccine without adjuv... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000789-39 | Sponsor Protocol Number: 116663 | Start Date*: 2012-06-28 | |||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||
Full Title: A Phase III, open, non-randomized, multi-centre, single dose study to assess immunogenicity and safety of Fluarix/Influsplit SSW 2012/2013 injected intramuscularly in adults (18 to 60 years) and in... | |||||||||||||
Medical condition: Immunization against Influenza of healthy adults | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011529-15 | Sponsor Protocol Number: GHB-CS04, VIE-CS-002 | Start Date*: 2010-05-26 | |||||||||||
Sponsor Name:AVIR Green Hills Biotechnology Research Development Trade AG | |||||||||||||
Full Title: A Phase II Prospective, Randomised, Double-Blind, Placebo-Controlled Study to Assess the Efficacy of the Influenza Vaccine GHB11L1 Administered Intranasally Against a Controlled Influenza Virus Cha... | |||||||||||||
Medical condition: Prophylaxis of Influenza A (H1N1) infection. | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005324-93 | Sponsor Protocol Number: CSLCT-NHF-08-55 | Start Date*: 2008-09-23 | |||||||||||
Sponsor Name:CSL Limited | |||||||||||||
Full Title: A Single Centre, Open-Label Study to Evaluate the Immunogenicity and Safety of Enzira® vaccine in Healthy ‘Adults’ aged ≥ 18 to < 60 years and in Healthy ‘Older Adults’ aged ≥ 60 years for the 2008... | |||||||||||||
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: 2013-001094-25 | Sponsor Protocol Number: 200188 | Start Date*: 2013-07-10 | |||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||
Full Title: A Phase III, open-label, non-randomised, multi-centre, single dose study to assess the immunogenicity and safety of GSK Biologicals' Quadrivalent Split Virion Influenza Vaccine (GSK2321138A) Influs... | |||||||||||||
Medical condition: Immunization of healthy adults against influenza | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003592-35 | Sponsor Protocol Number: LAIVImmuno | Start Date*: 2014-04-07 | |||||||||||||||||||||||||||||||
Sponsor Name:Public Health England | |||||||||||||||||||||||||||||||||
Full Title: A phase III/IV open-label study of the immunogenicity and safety of a single dose of a Live Attenuated Influenza Vaccine (LAIV) (FluenzTM) for each of three successive years in children naïve to, o... | |||||||||||||||||||||||||||||||||
Medical condition: Protection against influenza in healthy children | |||||||||||||||||||||||||||||||||
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Population Age: Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-001186-33 | Sponsor Protocol Number: AIV_FLU_2019_01_VIGIRA_JDD | Start Date*: 2019-09-27 |
Sponsor Name:FISABIO | ||
Full Title: Clinical trial, phase IV, randomized, double-blind, controlled, in children aged 12 to 35 months, of the vaccine against seasonal influenza to estimate efficacy against influenza and other respirat... | ||
Medical condition: Flu and acute respiratory infections | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-003655-74 | Sponsor Protocol Number: FluvalAB-H-YL2008 | Start Date*: 2008-08-18 | |||||||||||
Sponsor Name:Omninvest Ltd. | |||||||||||||
Full Title: FluvalAB Seasonal Influenza Vaccine Serologic Clinical Trial for 2008-2009 Influenza Season | |||||||||||||
Medical condition: Immunization of healthy people against influenza virus infections. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012555-22 | Sponsor Protocol Number: FluvalAB-H-YL2009 | Start Date*: 2009-08-13 | |||||||||||
Sponsor Name:Omninvest Ltd. | |||||||||||||
Full Title: Serologic Study of FluvalAB Influenza Vaccine (Trivalent, Seasonal) intended to Use in the 2009-2010 Vaccination Season | |||||||||||||
Medical condition: Immunization of healthy people against influenza virus infections. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000218-12 | Sponsor Protocol Number: V118_05 | Start Date*: 2013-09-17 | |||||||||||
Sponsor Name:Seqirus UK Limited | |||||||||||||
Full Title: A Phase III, Stratified, Randomized, Observer Blind, Controlled, Multicenter Clinical Study to Evaluate the Safety, Immunogenicity and Efficacy of an Adjuvanted Quadrivalent Subunit Influenza Virus... | |||||||||||||
Medical condition: Prophylaxis for influenza virus | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) IT (Completed) ES (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: 2013-003155-38 | Sponsor Protocol Number: 116926 | Start Date*: 2015-05-27 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A Phase III, double-blind, randomised, controlled, multi-country, multi-centre study to evaluate the immunogenicity and safety of GSK Biologicals’ quadrivalent influenza vaccine candidate, GSK22825... | ||
Medical condition: Healthy volunteers (Immunisation against influenza in male and female subjects 6 to 35 months of age inclusive) | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
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 |
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