- Trials with a EudraCT protocol (393)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
393 result(s) found for: Influenza B.
Displaying page 1 of 20.
EudraCT Number: 2017-003467-34 | Sponsor Protocol Number: FinFLU_HCPimmu_2017THL | Start Date*: 2017-10-17 | ||||||||||||||||
Sponsor Name:Terveyden ja hyvinvoinnin laitos (THL) | ||||||||||||||||||
Full Title: Immune responses to influenza vaccinations and viruses among health care personnel | ||||||||||||||||||
Medical condition: | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004063-66 | Sponsor Protocol Number: V87P2 | Start Date*: 2006-10-30 | |||||||||||
Sponsor Name:CHIRON | |||||||||||||
Full Title: A Phase II, Randomized, Controlled, Observer-blind, Single-Center Study to Evaluate Safety and Immunogenicity of Two Doses, Administered Three Weeks Apart, and a Six Month Booster Dose of Two FLUAD... | |||||||||||||
Medical condition: Active influenza profilaxis pandemic strain | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
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: 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: 2007-000165-38 | Sponsor Protocol Number: V87P1E1 | Start Date*: 2007-06-22 | |||||||||||
Sponsor Name:NOVARTIS VACCINES AND DIAGNOSTICS S.R.L. | |||||||||||||
Full Title: A Phase II, Open-label, Multi-Center Study to Evaluate Safety and Immunogenicity of a Booster Dose of FLUAD-H5N1 (Surface Antigen Adjuvanted with MF59C.1) Influenza Vaccine in Non-elderly Adult an... | |||||||||||||
Medical condition: Active immunoprofilaxis against potential pandemic influenza strain. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003314-16 | Sponsor Protocol Number: FLUVALAB-H-15 | Start Date*: 2011-08-30 | |||||||||||
Sponsor Name:Omninvest Ltd. | |||||||||||||
Full Title: A Randomized, Active Controlled, Double-blind, Multi-Centre Study to Evaluate Safety and Immunogenicity of One Dose of FLUVAL AB-like (Trivalent, Whole Virus, Aluminium Phosphate Gel Adjuvanted) In... | |||||||||||||
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: 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: 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: 2019-004721-24 | Sponsor Protocol Number: QHD00014 | Start Date*: 2020-09-07 | |||||||||||
Sponsor Name:Sanofi Pasteur Inc. | |||||||||||||
Full Title: Efficacy, Immunogenicity, and Safety of High-Dose Quadrivalent Influenza Vaccine Compared with Standard-Dose Quadrivalent Influenza Vaccine in Children 6 Months through 35 Months of Age | |||||||||||||
Medical condition: Prevention of influenza infection in children 6 months through 35 months of age | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: (No results available) |
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: 2012-004072-19 | Sponsor Protocol Number: Acti-INSP-001 | Start Date*: 2012-12-28 | |||||||||||
Sponsor Name:Vectura GmbH | |||||||||||||
Full Title: A randomized, double-blind, parallel group, placebo controlled Phase II study to evaluate the safety and efficacy of inhaled LASAG and Placebo, applied three times daily in adult hospitalized patie... | |||||||||||||
Medical condition: Influenza A and B | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) CZ (Prematurely Ended) HU (Prematurely Ended) SK (Prematurely Ended) ES (Prematurely Ended) LV (Prematurely Ended) LT (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
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: 2006-003181-34 | Sponsor Protocol Number: V70P2 | Start Date*: 2006-10-06 | |||||||||||
Sponsor Name:Novartis Vaccines and Diagnostics S.r.l. | |||||||||||||
Full Title: A Phase II, Observer-Blind, Randomized, Parallel Groups, Single Center, Exploratory Clinical Study to Evaluate the Immunogenicity and Safety of One and Two 0.25 mL Intramuscular Doses of FLUAD™ ve... | |||||||||||||
Medical condition: Influenza (vaccine trial) | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
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: 2006-006307-37 | Sponsor Protocol Number: 810601 | Start Date*: 2007-05-15 | |||||||||||
Sponsor Name:Baxter Innovations GmbH | |||||||||||||
Full Title: AN OPEN LABEL PHASE III STUDY OF A VERO CELL-DERIVED WHOLE VIRUS H5N1 INFLUENZA VACCINE TO ASSESS THE IMMUNOGENICITY AND SAFETY AND TO INVESTIGATE THE NEED FOR AND TIMING OF A BOOSTER VACCINATION | |||||||||||||
Medical condition: H5N1 Influenza vaccination in healthy subjects | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002861-11 | Sponsor Protocol Number: FID01C | Start Date*: 2007-08-10 | |||||||||||
Sponsor Name:Sanofi Pasteur MSD | |||||||||||||
Full Title: An Open-label, Multi-centre, Randomised, Comparative Study of the Immunogenicity and Safety of an Inactivated Split-Virion Influenza Vaccine administered by Intradermal Route (Flu-ID 15μg) versus a... | |||||||||||||
Medical condition: prevention, vaccination against Influenza in subjects 65 years or older via intradermal route | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001638-12 | Sponsor Protocol Number: mRNA-1010-P302 | Start Date*: 2022-09-29 | |||||||||||
Sponsor Name:ModernaTX, Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Observer-blind, Active-controlled Study to Evaluate the Safety and Efficacy of mRNA-1010 Candidate Seasonal Influenza Vaccine in Adults 50 Years and Older. | |||||||||||||
Medical condition: Influenza | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) EE (Completed) BG (Completed) DK (Completed) PL (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: 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 |
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