- Trials with a EudraCT protocol (45)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
45 result(s) found for: Pneumovax Vaccine.
Displaying page 1 of 3.
EudraCT Number: 2005-002789-12 | Sponsor Protocol Number: U05-PnPS-403 | Start Date*: 2005-09-28 |
Sponsor Name:Sanofi Pasteur MSD S.N.C | ||
Full Title: A double blind comparative and randomised study in healthy adults of the safety, tolerability, and immunogenicity of PNEUMOVAX®II formulated with either all new process polysaccharides or all curre... | ||
Medical condition: Prevention of invasive pneumococcal disease (IPD) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-002657-30 | Sponsor Protocol Number: WS2287576 | Start Date*: 2012-09-12 |
Sponsor Name:HYKS-instituutti | ||
Full Title: Immunogenicity of repeated dose 13-valent pneumococcal conjugate vaccine compared to the existing recommended protocol of pneumococcal polysaccharide vaccine in adult kidney and liver transplant pa... | ||
Medical condition: Immunogenicity of pneumococcal vaccines in liver and kidney transplant patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-000560-93 | Sponsor Protocol Number: 106623 | Start Date*: 2006-06-27 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A phase IIIa, open, multicentre study to evaluate the immunological memory induced in healthy children following a 3-dose primary vaccination with either GSK Biologicals’ 10-valent pneumococcal con... | ||
Medical condition: A single dose of Sanofi Pasteur MSD’s unconjugated 23-valent polysaccharide pneumococcal vaccine (Pneumovax™23) to healthy children who were previously primed with the full three doses of GSK Biolo... | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-003007-29 | Sponsor Protocol Number: 2014-0087054 | Start Date*: 2015-08-12 |
Sponsor Name:University Hospitals Leuven, department of pediatrics | ||
Full Title: The Polysaccharide Antibody Response Study: Typhim Vi response and allohemagglutinins versus Pneumo 23 vaccine response in the diagnosis of Specific Polysaccharide Antibody Deficiency. | ||
Medical condition: Specific polysaccharide antibody deficiency. | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-003052-36 | Sponsor Protocol Number: 105555 | Start Date*: 2005-11-18 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A phase II, multicentre booster study to evaluate booster vaccination with GSK Biologicals’ 10-valent pneumococcal conjugate vaccine or to evaluate the immune memory following the administration of... | ||
Medical condition: Booster vaccination against Streptococcus pneumoniae in healthy children having previously received vaccines as a primary 3-dose vaccination course in the study 11PN-PD-DIT-002. | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-000344-26 | Sponsor Protocol Number: V211-012-00 | Start Date*: 2007-06-04 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: A Phase III Double-Blind, Randomized Multicenter Study to Evaluate the Safety, Tolerability and Immunogenicity of ZOSTAVAX administered comcomitantly versus Non-concomitantly with PNEUMOVAX 23 in s... | |||||||||||||
Medical condition: herpes zoster, pneumococcal infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) GB (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018596-24 | Sponsor Protocol Number: 6311 | Start Date*: 2011-05-19 |
Sponsor Name:Oxford Radcliffe Hospital NHS Trust | ||
Full Title: Assessment of Salmonella Typhim Vi(TM) vaccine (Sanofi Pasteur MSD) for the investigation of selective antibody deficiency to polysaccharide. | ||
Medical condition: Suspected primary antibody deficiency states will be investigated | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2014-004013-85 | Sponsor Protocol Number: ZKSJ0073 | Start Date*: 2016-03-21 | |||||||||||
Sponsor Name:Friedrich Schiller University Jena | |||||||||||||
Full Title: Sequential versus simultaneous vaccination with pneumococcal conjugate vaccine (PCV13) and pneumococcal polysaccharide vaccine (PPV23) in unvaccinated older adults: Immunological memory and antibod... | |||||||||||||
Medical condition: previously unvaccinated older healthy adults | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005314-19 | Sponsor Protocol Number: 116889 | Start Date*: 2014-01-30 | ||||||||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | ||||||||||||||||||
Full Title: A phase III, randomized, open-label, multicenter clinical trial to assess the immunogenicity and safety of GSK Biologicals’ Herpes Zoster vaccine GSK1437173A when co-administered with Pneumovax 23 ... | ||||||||||||||||||
Medical condition: Healthy volunteers (Prevention of Herpes Zoster [HZ] and related complications in adults ≥ 50 years of age [YOA ] and immunocompromised adults ≥ 18 YOA.) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: EE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-004024-30 | Sponsor Protocol Number: V114-016 | Start Date*: 2018-08-01 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-blind, Active Comparatorcontrolled Study to Evaluate the Safety, Tolerability, and Immunogenicity of V114 Followed by Administration of PNEUMOVAX™23 One Y... | |||||||||||||
Medical condition: Pneumococcal disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023313-57 | Sponsor Protocol Number: INF | Start Date*: 2012-04-10 |
Sponsor Name:Helsinki University Central Hospital | ||
Full Title: Homing potential of the antigen specific B cell and antibody mediated immune response after vaccination | ||
Medical condition: Basic healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-003620-16 | Sponsor Protocol Number: IIV-465 | Start Date*: 2021-05-27 |
Sponsor Name:National Institute of Health and the Environment | ||
Full Title: Vaccine immunogenicity in Dutch frail versus non-frail older individuals (participating in the Doetinchem Cohort study) | ||
Medical condition: Older adults 73-79 years of age, birth cohorts year 1941-1947, still participating in round 6 of the Doetinchem Cohort Study. | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-007605-37 | Sponsor Protocol Number: 112807 | Start Date*: 2009-05-12 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A phase III, open, multicentre, extension study to assess the immune response following administration of an additional dose of GSK Biologicals’ 10-valent conjugate pneumococcal vaccine or Prevenar... | ||
Medical condition: A single dose of either 10Pn-PD-DiT or Prevenar vaccine to healthy children previously primed with 3 primary doses of 10Pn-PD-DiT or Prevenar vaccine in study 10PN-PD-DIT-003 (105554) and a booster... | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-004542-18 | Sponsor Protocol Number: V114-002 | Start Date*: 2012-04-04 | ||||||||||||||||||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | ||||||||||||||||||||||||||||
Full Title: A Multicenter, Double-Blind Study of the Safety, Tolerability, and Immunogenicity of a Pneumococcal Conjugate Vaccine (V114) Compared to Pneumococcal Polysaccharide Vaccine (PNEUMOVAX ™ 23) and ... | ||||||||||||||||||||||||||||
Medical condition: prevention of invasive pneumococcal disease and pneumococcal pneumonia caused by S. pneumoniae due to capsular serotypes included in the vaccine (4, 6B, 9V, 14, 18C, 19F, 1, 5, 7F, 3, 6A, 19A, 22F,... | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: SE (Completed) ES (Completed) PL (Completed) DK (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-003761-16 | Sponsor Protocol Number: 9818P | Start Date*: 2005-11-24 |
Sponsor Name:Department of R & D, Central Manchester and Manchester Children's Hospital NHS Trust | ||
Full Title: Evaluation of pneumococcal conjugate vaccine (Prevenar) in patients with myeloma and chronic lymphocytic leukaemia | ||
Medical condition: Pneumococcal disease is a common form of meningitis, septicaemia and pneumonia. Those individuals at highest risk include children, the elderly and persons whose immune systems are impaired. This l... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-001656-29 | Sponsor Protocol Number: V110-018 | Start Date*: 2015-04-21 |
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | ||
Full Title: A Phase III, Open-Label Clinical Trial to Study the Safety and Immunogenicity of V110 in Subjects 50 Years of Age and Older and in Subjects 2 to 49 Years of Age at Increased Risk for Pneumococcal D... | ||
Medical condition: Vaccination against pneumococcal disease caused by the 23 serotypes included in the vaccine | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2017-001909-32 | Sponsor Protocol Number: V114-018 | Start Date*: 2018-07-31 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-blind, Active Comparator controlled Study to Evaluate the Safety, Tolerability, and Immunogenicity of V114 Followed by Administration of PNEUMOVAX™23 Eigh... | |||||||||||||
Medical condition: Pneumococcal disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000260-99 | Sponsor Protocol Number: 10102010 | Start Date*: 2011-04-12 |
Sponsor Name:Department of Genitourinary medicine and Infectious Diseases, St James's Hospital, Dublin 8 | ||
Full Title: Immunogenicity of pneumococcal vaccination after prime boosting in HIV-Infected Adults: A Randomised Controlled Trial | ||
Medical condition: The primary objectives of this study are to: 1. Prospectively evaluate immunological response to vaccination with the 23-valent polysaccharide vaccine (PPV23) in HIV infected patients over a one y... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: IE (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-001299-79 | Sponsor Protocol Number: IMVX2014 | Start Date*: 2014-10-06 | |||||||||||
Sponsor Name:Department of Infectious Diseases, Odense University Hospital | |||||||||||||
Full Title: Pneumococcal vaccination of rheumatoid arthritis patients in immunomodulatory therapy | |||||||||||||
Medical condition: Immunoresponse on pneumococcal vaccination of rheumatoid arthritis patients in immunomodulatory therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004123-23 | Sponsor Protocol Number: Immunovax_Renal | Start Date*: 2017-04-20 | |||||||||||||||||||||
Sponsor Name:Department of Infectious Diseases, Odense University Hospital | |||||||||||||||||||||||
Full Title: Immunization of immunosuppressed patients – Knowledge, practices and serological response | |||||||||||||||||||||||
Medical condition: Immunoresponse on pneumococcal vaccination of kidney transplant recipients in immunomodulatory therapy or patients with end stage renal disease. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: View results |
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