- Trials with a EudraCT protocol (171)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
171 result(s) found for: H1N1 Influenza Virus.
Displaying page 3 of 9.
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: 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 |
EudraCT Number: 2009-016268-35 | Sponsor Protocol Number: 113883 | Start Date*: 2009-12-09 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A phase II, randomized, observer blind study to evaluate the safety and immunogenicity of three different vaccination schedules employing two formulations of the monovalent A/California/7/2009 (H1N... | ||
Medical condition: Immunization of healthy children aged 10 to less than 18 years against A/California/7/2009 (H1N1)v-like influenza | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: SK (Completed) EE (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: 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: 2022-000577-11 | Sponsor Protocol Number: VAP00027 | Start Date*: 2022-07-29 | |||||||||||
Sponsor Name:Sanofi Pasteur Inc | |||||||||||||
Full Title: Immunogenicity and Safety of Quadrivalent Recombinant Influenza Vaccine (RIV4) in Children and Adolescents Aged 9 to 17 Years and Adults Aged 18 to 49 Years | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) PL (Completed) DK (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021071-83 | Sponsor Protocol Number: FluvalAB-H-YL2010 | Start Date*: 2010-08-12 | |||||||||||
Sponsor Name:Omninvest Ltd. | |||||||||||||
Full Title: Tolerability and Immunogenicity Study of FluvalAB Influenza Vaccine (trivalent, seasonal, active ingredient content: 15 μg HA/strain/0.5 mL) in Adults and Elderly Person | |||||||||||||
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: 2012-001032-57 | 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: 2009-016078-33 | Sponsor Protocol Number: 113866 | Start Date*: 2009-10-06 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A phase III, observer-blind, randomised trial to evaluate the safety and immunogenicity of a two-dose schedule of the A/California/7/2009 (H1N1)v-like candidate vaccine manufactured in Dresden adju... | ||
Medical condition: Immunisation against A/California/7/2009 (H1N1)v-like influenza in male and female subjects aged 18 to 60 years. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-000728-27 | Sponsor Protocol Number: V118_18 | Start Date*: 2015-09-30 | |||||||||||
Sponsor Name:Seqirus UK Limited | |||||||||||||
Full Title: A Phase III, Randomized, Observer-Blind, Controlled, Multicenter Clinical Study to Evaluate the Efficacy, Safety and Immunogenicity of an MF59-Adjuvanted Quadrivalent Influenza Vaccine Compared to ... | |||||||||||||
Medical condition: Profylaxis for Influenza virus | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) PL (Completed) LV (Completed) CZ (Completed) LT (Completed) RO (Completed) BG (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: 2010-020083-38 | Sponsor Protocol Number: NV25118 | Start Date*: 2010-10-12 | ||||||||||||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | ||||||||||||||||||||||||||||
Full Title: A Multicenter, Study of the Safety of Oseltamivir Administered Intravenously for the Treatment of Influenza in Patients Aged ≥13 Years | ||||||||||||||||||||||||||||
Medical condition: Treatment of Influenza [seasonal or pandemic (H1N1) 2009] | ||||||||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: HU (Completed) DE (Completed) LT (Prematurely Ended) DK (Prematurely Ended) FR (Ongoing) IT (Prematurely Ended) ES (Prematurely Ended) PL (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-013837-92 | Sponsor Protocol Number: 113459 | Start Date*: 2010-09-04 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A phase III, open, randomized, trial to evaluate the immunogenicity and safety of a single or two-dose schedule of the A/California/7/2009 (H1N1)v-like candidate vaccine manufactured in Dresden adj... | ||
Medical condition: Immunization against A/California/7/2009 (H1N1)v-like influenza in male and female subjects aged 18 years and above. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-016226-13 | Sponsor Protocol Number: ANRS 151 | Start Date*: 2009-10-15 | ||||||||||||||||
Sponsor Name:Agence nationale de recherches sur le sida et les hépatites virales | ||||||||||||||||||
Full Title: Etude de phase II randomisée évaluant l'immunogénicité et la tolérance du vaccin antigrippal A(H1N1)v adjuvanté comparativement au vaccin antigrippal A(H1N1)v non adjuvanté chez des patients infect... | ||||||||||||||||||
Medical condition: infection VIH et vaccination anti-grippe A (H1N1) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (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: 2009-015960-32 | Sponsor Protocol Number: 113810 | Start Date*: 2009-11-26 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A phase III, randomised, observer-blind, multicentre study to evaluate the immunogenicity and safety of a 2-dose vaccination with the new process manufactured adjuvanted pandemic H1N1 influenza can... | ||
Medical condition: Immunisation of healthy children aged 3 years to 9 years against novel H1N1 influenza of pandemic potential. | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: CZ (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: 2016-002883-15 | Sponsor Protocol Number: V130_12 | Start Date*: 2017-07-19 | |||||||||||
Sponsor Name:Seqirus UK Limited | |||||||||||||
Full Title: A Phase III/IV, Stratified, Randomized, Observer Blind, Multicenter Clinical Study to Evaluate the Efficacy, Safety and Immunogenicity of a Cell-Based Quadrivalent Subunit Influenza Virus Vaccine C... | |||||||||||||
Medical condition: Profylaxis for Influenza virus | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) EE (Completed) ES (Completed) FI (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002712-25 | Sponsor Protocol Number: V101P1 | Start Date*: 2007-10-29 |
Sponsor Name:Novartis Vaccines and Diagnostics GmbH & Co. KG | ||
Full Title: A Phase II, Randomized, Placebo-controlled, Observer-blind, Multi Center Study on the Safety and Immunogenicity of Novartis Tetravalent Influenza Vaccine (containing both interpandemic strains and ... | ||
Medical condition: Avian Influenza | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
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