- Trials with a EudraCT protocol (284)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
284 result(s) found for: Influenza C virus.
Displaying page 1 of 15.
EudraCT Number: 2018-001857-29 | Sponsor Protocol Number: V130_14 | Start Date*: 2019-03-13 | |||||||||||
Sponsor Name:Seqirus UK Limited | |||||||||||||
Full Title: A Phase III, Randomized, Observer-blind, Multicenter Study to Evaluate the Efficacy, Immunogenicity and Safety of Seqirus' Cell-Based Quadrivalent Subunit Influenza Virus Vaccine (QIVc) Compared to... | |||||||||||||
Medical condition: Prophylaxis of influenza virus infection | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) EE (Completed) CZ (Completed) LV (Completed) PL (Completed) Outside EU/EEA RO (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000785-21 | Sponsor Protocol Number: GQM11 | Start Date*: 2014-07-24 | |||||||||||
Sponsor Name:Sanofi Pasteur | |||||||||||||
Full Title: Immunogenicity and Lot-to-Lot Consistency Study of a Quadrivalent Influenza Vaccine in Adult and Elderly Subjects | |||||||||||||
Medical condition: Prevention of influenza infection in adults from 18 years of age | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (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: 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: 2016-000425-40 | Sponsor Protocol Number: GV29893 | Start Date*: 2016-08-03 | |||||||||||||||||||||
Sponsor Name:Genentech Inc. | |||||||||||||||||||||||
Full Title: A PHASE 2 RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL OF MHAA4549A, A MONOCLONAL ANTIBODY, ADMINISTERED AS MONOTHERAPY FOR THE TREATMENT OF ACUTE UNCOMPLICATED SEASONAL INFLUENZA A INFECTION... | |||||||||||||||||||||||
Medical condition: acute uncomplicated seasonal influenza | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-005101-79 | Sponsor Protocol Number: GQM04 | Start Date*: 2012-10-05 | |||||||||||
Sponsor Name:Sanofi Pasteur | |||||||||||||
Full Title: Safety and Immunogenicity of a Quadrivalent Influenza Vaccine Administered via the Intramuscular Route in Child/Adolescent and Adult Subjects | |||||||||||||
Medical condition: Prophylaxis of influenza in subjects from 9-17 years of age (and adults aged 18 to 60 years). | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001974-27 | Sponsor Protocol Number: STOPFLU | Start Date*: 2019-10-15 | |||||||||||||||||||||
Sponsor Name:Centre Hospitalier Universitaire Vaudois (CHUV) | |||||||||||||||||||||||
Full Title: Reducing the Burden of Influenza after Solid-Organ Transplantation: the STOP-FLU trial [Swiss Trial in solid Organ transplantation on Prevention of inFLUenza] | |||||||||||||||||||||||
Medical condition: Influenza in solid organ transplant patients | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001008-49 | Sponsor Protocol Number: NV22155 | Start Date*: 2016-09-30 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche AG | |||||||||||||
Full Title: A randomized, multicenter trial of oseltamivir doses of 75 mg for 5 or 10 days versus 150 mg for 5 or 10 days in influenza patients with pandemic (H1N1) 2009 | |||||||||||||
Medical condition: Influenza | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000461-43 | Sponsor Protocol Number: GV29216 | Start Date*: 2014-12-22 | |||||||||||||||||||||
Sponsor Name:Genentech Inc. | |||||||||||||||||||||||
Full Title: A PHASE 2 RANDOMIZED, DOUBLE-BLIND TRIAL OF MHAA4549A, A MONOCLONAL ANTIBODY IN COMBINATION WITH OSELTAMIVIR VERSUS OSELTAMIVIR FOR TREATMENT OF SEVERE INFLUENZA A INFECTION | |||||||||||||||||||||||
Medical condition: Treatment of Influenza | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Prematurely Ended) GB (Completed) HU (Completed) DE (Completed) CZ (Prematurely Ended) ES (Completed) BE (Completed) NL (Completed) BG (Prematurely Ended) PL (Completed) FR (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-001044-18 | Sponsor Protocol Number: ML22789 | Start Date*: 2016-10-03 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche AG | |||||||||||||
Full Title: A phase IIIb, openlabel, comparative, randomized study on resistance of Influenza A/H1N1 2009 virus to treatment with Oseltamivir at standard dose versus double dose | |||||||||||||
Medical condition: Influenza A/H1N1 | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001231-51 | Sponsor Protocol Number: GQM05 | Start Date*: 2014-05-20 | |||||||||||
Sponsor Name:Sanofi Pasteur | |||||||||||||
Full Title: Efficacy and Immunogenicity Study of Quadrivalent Influenza Vaccine Administered via the Intramuscular Route in Healthy Children Aged 6 to 35 Months | |||||||||||||
Medical condition: Prevention of influenza infection in children aged 6 to 35 months | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) ES (Completed) GR (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005243-25 | Sponsor Protocol Number: GID37 | Start Date*: 2013-04-16 | |||||||||||
Sponsor Name:Sanofi Pasteur | |||||||||||||
Full Title: Immunogenicity and Safety of the Trivalent Influenza Vaccine (Split-Virion, Inactivated), Northern Hemisphere 2013-2014 Formulation (Intradermal Route) | |||||||||||||
Medical condition: Prophylaxis of influenza (2013-2014 Northern Hemisphere Season) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (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: 2014-000966-23 | Sponsor Protocol Number: BCG_influenza | Start Date*: 2014-05-30 | |||||||||||
Sponsor Name:Radboud University Nijmegen Medical Centre | |||||||||||||
Full Title: The effects of BCG-vaccination on the immune response induced by influenza-vaccination in healthy volunteers A pilot proof-of-principle study | |||||||||||||
Medical condition: Influenza virus infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002169-21 | Sponsor Protocol Number: CP40563 | Start Date*: 2018-11-19 | ||||||||||||||||||||||||||
Sponsor Name:Roche Farma SA que realiza un el ensayo en España y que actúa como representante de F. Hoffmann-La Roche Ltd | ||||||||||||||||||||||||||||
Full Title: A MULTICENTER, RANDOMIZED, DOUBLE-BLIND, ACTIVE (OSELTAMIVIR)-CONTROLLED STUDY TO ASSESS THE SAFETY, PHARMACOKINETICS, AND EFFICACY OF BALOXAVIR MARBOXIL IN OTHERWISE HEALTHY PEDIATRIC PATIENTS 1 T... | ||||||||||||||||||||||||||||
Medical condition: Influenza | ||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: ES (Completed) PL (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-002599-95 | Sponsor Protocol Number: V118_05E1 | Start Date*: 2014-09-19 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A Phase III, Randomized, Observer Blind, Multicenter Study to Evaluate the Safety and Immunogenicity of Repeated Exposure to an Adjuvanted Quadrivalent Subunit Influenza Virus Vaccine (aQIV), Admin... | |||||||||||||
Medical condition: Prophylaxis for influenza virus | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005929-49 | Sponsor Protocol Number: VX11-787-101 | Start Date*: 2012-02-20 | |||||||||||
Sponsor Name:Vertex Pharmaceuticals Incorporated | |||||||||||||
Full Title: A Phase 2a, Randomized, Double Blind, Placebo Controlled Study to Investigate the Effects of VX 787 Administered to Adult Volunteers Experimentally Inoculated with Live Influenza Virus | |||||||||||||
Medical condition: Influenza A | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000629-19 | Sponsor Protocol Number: GID47 | Start Date*: 2014-08-21 | |||||||||||
Sponsor Name:Sanofi Pasteur | |||||||||||||
Full Title: Safety assessment of the Trivalent Influenza Vaccine (Split-Virion, Inactivated), Northern Hemisphere 2014-2015 Formulation (Intradermal Route) | |||||||||||||
Medical condition: Prophylaxis of influenza (2014-2015 Northern Hemisphere Season) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000576-19 | Sponsor Protocol Number: VAP00026 | Start Date*: 2022-07-29 | |||||||||||
Sponsor Name:Sanofi Pasteur Inc | |||||||||||||
Full Title: Immunogenicity and Safety of Quadrivalent Recombinant Influenza Vaccine Compared with Egg-Based Standard-Dose Quadrivalent Influenza Vaccine in Children 3 to 8 Years of Age. | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) PL (Prematurely Ended) DK (Prematurely Ended) CZ (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001863-11 | Sponsor Protocol Number: EWO-ISO-2014/1 | Start Date*: 2014-09-24 | |||||||||||
Sponsor Name:Ewopharma AG. | |||||||||||||
Full Title: A Phase 4, Randomised, Placebo-Controlled, Double-Blind, Multicenter Study to Evaluate Efficacy of Isoprinosine® in Comparison With Placebo in Subjects With Confirmed Acute Respiratory Viral Infect... | |||||||||||||
Medical condition: Acute Respiratory Viral Infections due to influenza A or B virus, RSV, adenovirus, or parainfluenza virus 1 or 3 | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
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