- Trials with a EudraCT protocol (148)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (9)
148 result(s) found for: Polio vaccine.
Displaying page 1 of 8.
EudraCT Number: 2015-005190-21 | Sponsor Protocol Number: TD525 | Start Date*: 2015-11-19 |
Sponsor Name:Sanofi Pasteur SA | ||
Full Title: Immunogenicity and Safety of ADACEL Polio (TdcP-IPV Vaccine) Administered at 6 to 8 Years of Age as a Fifth Dose (Pre-School Booster) in Healthy Children in Taiwan | ||
Medical condition: Diphtheria Tetanus Pertussis Poliomyelitis | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2007-000199-17 | Sponsor Protocol Number: SM07-01 | Start Date*: Information not available in EudraCT |
Sponsor Name:Norwegian Institute of Public Health | ||
Full Title: Open clinical study to assess the immune response and safety of a booster dose (5th dose) of a combination vaccine against diphteria-tetanus-pertussis-polio given to healthy adolescents 15-16 year... | ||
Medical condition: Profylactic vaccination against diphteria-, tetanus-, pertussis and polio in healthy volunteers 15-16 years old. These volunteers have previously been given a 4th dose of the same vaccine in a clin... | ||
Disease: | ||
Population Age: Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NO (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-005184-16 | Sponsor Protocol Number: IPV26 | Start Date*: 2015-11-17 |
Sponsor Name:Sanofi Pasteur SA | ||
Full Title: Immunogenicity and Safety of Fractional Booster Dose of sanofi pasteur’s Inactivated Poliomyelitis Vaccine (IMOVAX Polio) Administered Intradermally versus Full Booster Dose of Inactivated Poliomye... | ||
Medical condition: Poliomyelitis | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2015-005186-23 | Sponsor Protocol Number: IPV34 | Start Date*: 2015-11-19 |
Sponsor Name:Sanofi Pasteur China | ||
Full Title: Large scale safety study of IMOVAX Polio in selected cities in China, an observational post marketing study | ||
Medical condition: Poliomyelitis | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2015-005185-34 | Sponsor Protocol Number: IPV29 | Start Date*: 2015-11-19 |
Sponsor Name:Sanofi Pasteur China | ||
Full Title: Safety study of IMOVAX Polio in selected cities in China, an observational post marketing study | ||
Medical condition: Poliomyelitis | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2015-005183-42 | Sponsor Protocol Number: IPV25 | Start Date*: 2015-11-17 |
Sponsor Name:Sanofi Pasteur SA | ||
Full Title: Immunogenicity and Safety of Fractional Doses of Sanofi Pasteur’s Inactivated Poliomyelitis Vaccine (IMOVAX Polio™) Administered Intradermally versus Full Doses of Inactivated Poliomyelitis Vaccine... | ||
Medical condition: Poliomyelitis | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2015-003544-39 | Sponsor Protocol Number: M3-ABMG | Start Date*: 2015-10-21 | |||||||||||
Sponsor Name:FIDEC - Fighting Infectious Diseases in Emerging Countries | |||||||||||||
Full Title: A Phase 4 study to evaluate the safety and immunogenicity of monovalent oral polio vaccine type 2 in healthy IPV-vaccinated children aged 1 to 5 years in Lithuania | |||||||||||||
Medical condition: evaluation of safety of SABIN mOPV2 in healthy IPV-vaccinated children of 1 – 5 years of age (Polio disease) | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005187-42 | Sponsor Protocol Number: IPV35_EFC12403 | Start Date*: 2015-11-19 |
Sponsor Name:Sanofi Aventis K.K. | ||
Full Title: Immunogenicity and Safety of the SP059 Given Subcutaneously as a Three-Dose Primary and Booster Vaccination in Infants in Japan | ||
Medical condition: Poliomyelitis | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2015-005182-23 | Sponsor Protocol Number: IPV13 | Start Date*: 2015-11-17 |
Sponsor Name:Sanofi Pasteur SA | ||
Full Title: Immunogenicity and Safety of the Inactivated Poliomyelitis Vaccine (IMOVAX Polio™) Administered at 2, 3, and 4 Months of Age and Followed by a Booster Dose at 18 Months of age in Healthy Infants in... | ||
Medical condition: Poliomyelitis | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
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... | ||||||||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FR (Ongoing) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-003324-32 | Sponsor Protocol Number: UAT1 | Start Date*: 2015-09-18 | |||||||||||
Sponsor Name:University of Antwerp | |||||||||||||
Full Title: A Phase 4 study to evaluate the safety and immunogenicity of trivalent oral polio vaccine in adults previously vaccinated with oral polio vaccine | |||||||||||||
Medical condition: Historic tOPV can result in the emergence of circulating vaccine-derived polioviruses (cVDPVs): the attenuated strains of poliovirus from the vaccine infect un-immunized individuals, replicate, cir... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001684-22 | Sponsor Protocol Number: UAM4 | Start Date*: 2018-10-11 | |||||||||||
Sponsor Name:University of Antwerp | |||||||||||||
Full Title: A Phase 2, partial blind, randomized, placebo-controlled, multicenter study to evaluate the safety and immunogenicity of two novel live attenuated serotype 2 oral poliovirus vaccines candidates, in... | |||||||||||||
Medical condition: Poliomyelitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003279-31 | Sponsor Protocol Number: IPV46/EFC13614 | Start Date*: 2016-04-19 |
Sponsor Name:Sanofi K.K. | ||
Full Title: Immunogenicity and Safety of IMOVAX POLIO® Subcutaneous as a Booster Given in Pre-school Age Children in Japan (IPV46) | ||
Medical condition: Poliovirus types 1, 2, and 3 | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2008-002378-37 | Sponsor Protocol Number: LIS/IMM138 | Start Date*: 2008-12-23 |
Sponsor Name:National Institute of Health and the Environment (RIVM) | ||
Full Title: The longitudinal kinetics of long term cellular memory immunity against Bordetella pertussis in Dutch 8-9 years old children after ACV booster vaccination. | ||
Medical condition: Whooping cough is a respiratory disease caused by Bordetella pertussis. Young infants are mostly at risk, but older children are the main source of infection. Since the incidence of whooping cough... | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000052-29 | Sponsor Protocol Number: VIPV-04 | Start Date*: 2014-09-17 | |||||||||||
Sponsor Name:Statens Serum Institut | |||||||||||||
Full Title: Safety and immunogenicity of 3 adjuvated reduced dose inactivated poliovirus vaccines (IPV-Al SSI) and non-adjuvated full dose IPV SSI, given as a booster vaccination to adolescents with a hi... | |||||||||||||
Medical condition: Profylactic immunisation against poliomyelitis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003477-94 | Sponsor Protocol Number: 110947 | Start Date*: 2008-02-13 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A phase IV, open, non-randomised, multicentre study to assess the reactogenicity and immunogenicity of a booster dose of GSK Biologicals’ combined reduced-antigen-content diphtheria-tetanus, acellu... | ||
Medical condition: Booster immunisation against diphtheria, tetanus, pertussis and poliomyelitis diseases in children and adolescents. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-003325-33 | Sponsor Protocol Number: UAM1 | Start Date*: 2015-09-18 | |||||||||||
Sponsor Name:University of Antwerp | |||||||||||||
Full Title: A Phase 4 study to evaluate the safety and immunogenicity of monovalent oral polio vaccine type 2 in healthy OPV-vaccinated adults | |||||||||||||
Medical condition: Polio disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005188-17 | Sponsor Protocol Number: IPV30 | Start Date*: 2015-11-19 |
Sponsor Name:Sanofi Pasteur SA | ||
Full Title: Immunogenicity and Safety of different sequential schedules of Inactivated Poliomyelitis Vaccine (IMOVAX Polio®) followed by Oral Poliomyelitis Vaccine in Healthy Infants in China versus Oral Polio... | ||
Medical condition: Poliomyelitis | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2014-005077-36 | Sponsor Protocol Number: S2268 | Start Date*: 2015-05-08 |
Sponsor Name:Örebro Läns Landsting | ||
Full Title: Simplified basic immunisation after transplantation of stem cells | ||
Medical condition: Patients undergoing stem cell transplantation loose their protection from basic vaccinations done during childhood and need to be immunised again to be protected from diphteria, tetanus, polio and ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2021-006686-37 | Sponsor Protocol Number: SH600009 | Start Date*: 2022-02-18 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Sanofi Pasteur | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Immunogenicity and Safety of a DTwP-HepB-Hib-IPV (SHAN6™) Vaccine when Administered Concomitantly with Routine Pediatric Vaccines in Healthy Infants and Toddlers in Thailand | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Diphtheria, Tetanus, Pertussis, Hepatitis-B, invasive Haemophilus influenzae type b and Poliomyelitis diseases | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: Outside EU/EEA | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
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