- Trials with a EudraCT protocol (414)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (186)
414 result(s) found for: Tetanus.
Displaying page 1 of 21.
| EudraCT Number: 2018-003838-32 | Sponsor Protocol Number: ADC01 | Start Date*: 2019-01-11 |
| Sponsor Name:Sanofi Pasteur | ||
| Full Title: Safety and Immunogenicity of Tetanus Toxoid, Reduced Diphtheria Toxoid, and Acellular Pertussis Vaccine Adsorbed (SP0173) in Healthy Adolescents, Adults, and Older Adults | ||
| Medical condition: Tetanus Diphtheria Pertussis | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2015-005845-30 | Sponsor Protocol Number: Td506-LT | Start Date*: 2016-01-26 | |||||||||||||||||||||
| Sponsor Name:Sanofi Pasteur Limited | |||||||||||||||||||||||
| Full Title: One-, Three-, Five-, and Ten-Year Data on the Long-Term Immunogenicity of Tetanus Toxoid, Reduced Diphtheria Toxoid and Acellular Pertussis Vaccine Adsorbed (Tdap) in Adults and Adolescents (11-64 ... | |||||||||||||||||||||||
| Medical condition: Active immunization against tetanus, diphtheria and pertussis | |||||||||||||||||||||||
|
|||||||||||||||||||||||
| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2018-001604-10 | Sponsor Protocol Number: TriDiTe2018 | Start Date*: 2018-09-05 | ||||||||||||||||
| Sponsor Name:BIODRUG s.r.o. | ||||||||||||||||||
| Full Title: A single blind, randomized comparative and multicentre clinical trial of the immunogenicity and safety of booster immunisation with bivalent vaccine against tetanus and diphtheria VACDITE (BIODRUG)... | ||||||||||||||||||
| Medical condition: Verification of immune response after booster immunisation with one dose of vaccine against tetanus and diphtheriae | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: SK (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2015-005843-15 | Sponsor Protocol Number: Td9704-LT | Start Date*: 2016-01-26 | |||||||||||||||||||||
| Sponsor Name:Sanofi Pasteur Limited | |||||||||||||||||||||||
| Full Title: One-, Three-, Five-, Eight- and Ten-Year Data on the Long- Term Immunogenicity of Tetanus Toxoid, Reduced Diphtheria Toxoid and Acellular Pertussis Vaccine Adsorbed (Tdap) in Adults and Adolescents | |||||||||||||||||||||||
| Medical condition: Active immunization against tetanus, diphtheria and pertussis | |||||||||||||||||||||||
|
|||||||||||||||||||||||
| Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2015-005844-32 | Sponsor Protocol Number: Td9805-LT | Start Date*: 2016-01-26 | |||||||||||||||||||||
| Sponsor Name:Sanofi Pasteur Limited | |||||||||||||||||||||||
| Full Title: One-, Three-, Five- and Ten-Year Data on the Long-Term Immunogenicity of Tetanus Toxoid, Reduced Diphtheria Toxoid and Acellular Pertussis Vaccine Adsorbed (Tdap) in Adolescents 11–14 Years of Age | |||||||||||||||||||||||
| Medical condition: Active immunization against tetanus, diphtheria and pertussis | |||||||||||||||||||||||
|
|||||||||||||||||||||||
| Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2009-011742-26 | Sponsor Protocol Number: TetDip-2009 | Start Date*: 2009-04-14 | |||||||||||||||||||||
| Sponsor Name:Institute for Biomedical Aging Research | |||||||||||||||||||||||
| Full Title: Humoral and cellular immune response against tetanus and diphtheria following booster vaccination | |||||||||||||||||||||||
| Medical condition: This study will analyze cellular and humoral immune responses after booster vaccination. Healthy adults are vaccinated against tetanus, diphtheria, pertussis and polio on a regular basis. This stud... | |||||||||||||||||||||||
|
|||||||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: AT (Completed) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2011-004458-25 | Sponsor Protocol Number: RVX01C | Start Date*: Information not available in EudraCT | ||||||||||||||||||||||||||
| Sponsor Name:Sanofi Pasteur MSD | ||||||||||||||||||||||||||||
| Full Title: Antibody persistence in 11 to 13-year-old children previously vaccinated at 6 years old with either REVAXIS or DT Polio, and immune response to a booster dose of TETRAVAC-ACELLULAIRE | ||||||||||||||||||||||||||||
| Medical condition: Persistence of antibody against diphtheria, tetanus and poliomyelitis in 11 to 13-year-old children who received either REVAXIS or DT Polio at 6 year of age, and immune response to TETRAVAC-ACELLUL... | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: FR (Ongoing) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2008-008724-32 | Sponsor Protocol Number: RPV02C | Start Date*: 2009-06-08 | |||||||||||
| Sponsor Name:Sanofi Pasteur MSD S.N.C. | |||||||||||||
| Full Title: A randomised, comparative, multicentre clinical trial of the immunogenicity and safety of Tdap-IPV vaccine (REPEVAX) and a tetanus monovalent vaccine in healthy adults 18 years of age and older | |||||||||||||
| Medical condition: Antibody responses to tetanus toxoid. | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-005629-38 | Sponsor Protocol Number: Td551 | Start Date*: 2016-01-13 | |||||||||||||||||||||
| Sponsor Name:Sanofi Pasteur Inc. | |||||||||||||||||||||||
| Full Title: Immunogenicity of Adacel® and BOOSTRIX® Vaccines in Adolescents | |||||||||||||||||||||||
| Medical condition: Active immunization against tetanus, diphtheria and pertussis | |||||||||||||||||||||||
|
|||||||||||||||||||||||
| Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2015-005628-25 | Sponsor Protocol Number: Td540 | Start Date*: 2016-01-13 | |||||||||||||||||||||
| Sponsor Name:Sanofi-Aventis K.K. | |||||||||||||||||||||||
| Full Title: Immunogenicity and Safety of The tetanus toxoid, reduced diphtheria toxoid and acellular pertussis vaccine adsorbed (SP306) as a Booster in Japanese Adolescents | |||||||||||||||||||||||
| Medical condition: Active immunization against tetanus, diphtheria and pertussis | |||||||||||||||||||||||
|
|||||||||||||||||||||||
| Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2014-001995-71 | Sponsor Protocol Number: PLATIG-1404 | Start Date*: 2014-07-03 |
| Sponsor Name:Plazmaferezis Állomás Közhasznú Nonprofit Kft | ||
| Full Title: Open label multicenter prospective trial to assess the tetanus titer in subject of regular plasmapharesis | ||
| Medical condition: healthy subjects eligible for tetanus booster vaccination | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: HU (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-003941-24 | Sponsor Protocol Number: Td528 | Start Date*: 2016-01-13 | |||||||||||||||||||||
| Sponsor Name:SANOFI PASTEUR SA | |||||||||||||||||||||||
| Full Title: Immunogenicity and Safety of Sanofi Pasteur’s Tdap Combined Vaccine (ADACEL) as a Booster Dose, versus Local DT Vaccine in Healthy Children or versus Local Td Vaccine in Healthy Adolescents and Adu... | |||||||||||||||||||||||
| Medical condition: Active immunization against tetanus, diphtheria and pertussis | |||||||||||||||||||||||
|
|||||||||||||||||||||||
| Population Age: Children, Under 18, Adults | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2015-005589-43 | Sponsor Protocol Number: Td508 | Start Date*: 2016-01-12 | |||||||||||||||||||||
| Sponsor Name:Sanofi Pasteur Limited | |||||||||||||||||||||||
| Full Title: Safety and immunogenicity of Tetanus and Diphtheria Toxoids Adsorbed Combined with Component Pertussis (ADACEL™) Vaccine compared to Component Pertussis Vaccine and Diphtheria and Tetanus Toxoids A... | |||||||||||||||||||||||
| Medical condition: Active immunization against tetanus, diphtheria and pertussis | |||||||||||||||||||||||
|
|||||||||||||||||||||||
| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2015-003950-41 | Sponsor Protocol Number: Td536 | Start Date*: 2016-01-13 | |||||||||||||||||||||
| Sponsor Name:SANOFI PASTEUR SA | |||||||||||||||||||||||
| Full Title: Immunogenicity and safety of the tetanus toxoid, reduced diphtheria toxoid and acellular pertussis vaccine adsorbed (SP306) given intramuscularly compared to Diphtheria and Tetanus toxoids adsorbed... | |||||||||||||||||||||||
| Medical condition: Active immunization against tetanus, diphtheria and pertussis | |||||||||||||||||||||||
|
|||||||||||||||||||||||
| Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2014-004344-35 | Sponsor Protocol Number: 50993 | Start Date*: 2015-02-16 |
| Sponsor Name:Leiden University Medical Center | ||
| Full Title: The effect of tetanus revaccination in patients with myasthenia gravis | ||
| Medical condition: Myasthenia gravis Lambert-Eaton myasthenic syndrome | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-005842-69 | Sponsor Protocol Number: Td526 | Start Date*: 2016-01-26 | |||||||||||||||||||||
| Sponsor Name:Sanofi Pasteur Limited | |||||||||||||||||||||||
| Full Title: Immune Responses in Adults to Revaccination with Tetanus Toxoid, Reduced Diphtheria Toxoid and Acellular Pertussis Vaccine Adsorbed (ADACEL®) 10 Years After a Previous Dose | |||||||||||||||||||||||
| Medical condition: Active immunization against tetanus, diphtheria and pertussis | |||||||||||||||||||||||
|
|||||||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2015-005627-84 | Sponsor Protocol Number: Td519 | Start Date*: 2016-01-13 | |||||||||||||||||||||
| Sponsor Name:Sanofi Pasteur Inc. | |||||||||||||||||||||||
| Full Title: A pivotal open label, two-arm, multi-center trial to evaluate the safety and immunogenicity of a single dose of Adacel® vaccine in persons 10 to <11 years of age with the intent to extend the licen... | |||||||||||||||||||||||
| Medical condition: Active immunization against tetanus, diphtheria and pertussis | |||||||||||||||||||||||
|
|||||||||||||||||||||||
| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2010-023086-21 | Sponsor Protocol Number: RPV04C | Start Date*: 2010-12-13 | ||||||||||||||||||||||||||
| Sponsor Name:Sanofi Pasteur MSD S.N.C. | ||||||||||||||||||||||||||||
| Full Title: An open-label, multicentre study to evaluate the immunogenicity and safety of one dose of a diphtheria, tetanus, acellular pertussis and poliomyelitis vaccine (REPEVAX®) followed by 2 doses of a di... | ||||||||||||||||||||||||||||
| Medical condition: Evaluation of the immunogenicity and safety of one dose of a diphtheria, tetanus, acellular pertussis and poliomyelitis vaccine (REPEVAX®) followed by 2 doses of a diphtheria, tetanus and poliomyel... | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2015-005196-24 | Sponsor Protocol Number: TD9809-LT | Start Date*: 2015-11-19 |
| Sponsor Name:Sanofi Pasteur Limited | ||
| Full Title: Three-, Five-, and Ten-Year Data on the Long-Term Immunogenicity of Tetanus and Diphtheria Toxoids Adsorbed Combined with Component Pertussis Vaccine and Inactivated Poliomyelitis Vaccine (TdcP-IPV... | ||
| Medical condition: Pertussis Tetanus Diphtheria Poliomyelitis Hepatitis B | ||
| Disease: | ||
| Population Age: Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2016-004934-11 | Sponsor Protocol Number: TeVaTri042017 | Start Date*: 2017-03-02 |
| Sponsor Name:BIODRUG s.r.o. | ||
| Full Title: A single blind, randomized comparative and multicentre clinical trial of the immunogenicity and safety of booster immunisation with tetanus monovalent vaccines VACTETA 40 IU/0,5 ml (BIODRUG) and TE... | ||
| Medical condition: Verification of immune response after booster immunisation with one dose of tetanus monovalent vaccine | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: CZ (Completed) | ||
| Trial results: View results | ||
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
| Download Options: | |
|---|---|
| Number of Trials to download: | |
| Download Content: | |
| Download Format: | |
| Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. | |
Query did not match any studies.