tetanus

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Information
Disease name
tetanus
Disease ID
DOID:11338
Description
"A primary bacterial infectious disease that results in prolonged contraction of skeletal muscle fibers, has_material_basis_in Clostridium tetani, which produces tetanospasmin, a neurotoxin, which is carried to the brain and spinal cord, where it binds irreversibly to receptors inhibiting neurotransmission. Damaged upper motor neurons cannot control reflex responses to afferent sensory stimuli." [url:http\://en.wikipedia.org/wiki/Tetanus]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
Genes Mutation Description Source Links
NCT ID Status Phase Summary Start date Completion date
NCT06123663 Active, not recruiting Phase 1 A Study to Evaluate the Safety and Immunogenicity of a Single Dose of Adsorbed Tetanus Vaccine in a Population Aged 18 Years and Over December 20, 2023 July 2024
NCT05480462 Active, not recruiting Phase 3 Immunogenicity and Safety of Vaccine Against Tetanus and Diphtheria. December 12, 2022 June 2024
NCT05091619 Active, not recruiting Phase 3 A Phase 3 Study of BIBP Diphtheria, Tetanus and Acellular Pertussis (Three Components) Combined Vaccine, Adsorbed October 22, 2021 September 22, 2027
NCT00136604 Completed Phase 3 Response to GSK Biologicals' Tritanrix-HepB/Hib-MenAC Vacc (4th Dose) at 15-24m & Mencevax ACWY at 24-30m January 22, 2006 April 23, 2006
NCT00138268 Completed Pilot Study Freeze and Transport Immune Cells February 2005
NCT00146835 Completed Post-marketing Safety Study of GSK Biological's Pediarix™ Vaccine April 2003 June 2006
NCT00148941 Completed Phase 3 Immune Response and Safety Comparison of 3 Lots of GSK Biologicals' DTaP-IPV Candidate Vaccine to DTaP + IPV Vaccines January 6, 2005 December 4, 2006
NCT00158808 Completed Phase 2 Immune Memory Foll Pry Vaccination With DTPw-HBV/Hib Vaccine Formulation; Immuno & Reacto of Booster Dose at 15-18 Mths January 2005 April 2005
NCT00168545 Completed Phase 4 Immunology of Non-specific Effects of Vaccine January 2006 January 2007
NCT00169442 Completed Phase 3 Immune Memory of DTPw-HBV/Hib Vaccine Following Primary Vaccination, Immuno & Reacto of a Booster Dose Given in Infants February 10, 2005 March 10, 2006
NCT00197275 Completed Phase 3 Lot-to-lot Consistency of Tritanrix™-HepB/Hib-MenAC & Its Non-inferiority vs Tritanrix™-HepB/Hiberix™ in Infants February 2006 November 2006
NCT00228917 Completed Phase 3 Safety Study of Tritanrix-HepB/Hib-MenAC, Tritanrix-HepB/Hiberix, and Mencevax ACWY Vaccines in Children June 16, 2005 January 20, 2006
NCT00254917 Completed Phase 4 Assessment of the Immunogenicity and Safety of PENTAXIM™ in Philippines October 2003 February 2006
NCT00254969 Completed Phase 3 Immunogenicity and Safety of Pentaxim in South African Infants October 2005 January 2010
NCT00255021 Completed Phase 4 Immunogenicity and Safety of Sanofi Pasteur Pentaxim Combined Vaccine in Infants in Thailand December 2005 January 2009
NCT00258895 Completed Phase 3 Safety and Immunogenicity of DAPTACEL® as 5th Dose in Children 4 to 6 Years Old After 4 Doses of Pentacel™ or DAPTACEL® March 2005 April 2007
NCT00258908 Completed Phase 3 Immunogenicity and Safety of ADACEL™ as Fifth Dose in Taiwan November 2005 August 2006
NCT00259337 Completed Phase 3 Immunogenicity and Safety of Pentaxim™ in an Indian Population February 2006 December 2008
NCT00263679 Completed Phase 3 Assessment of GSK Biologicals' Tdap Candidate Vaccine Administered as a Booster (6th Dose) in Terms of Immunogenicity and Safety to Children and Adolescents Previously Vaccinated With Five Doses of an Acellular Pertussis-containing Vaccine. November 2003 October 2004
NCT00263692 Completed Phase 2 Comparison of GSK Biologicals' DTaP-IPV Candidate Vaccine to DTaP and IPV Separately Administered Vaccines in Terms of Immune Response and Safety November 2002 September 2004
NCT00282295 Completed Phase 4 US-licensed Combined Vaccine Against Tetanus & Diphtheria, Given With US-licensed Vaccine Against Meningococcal Disease January 25, 2006 August 8, 2006
NCT00287092 Completed Phase 3 Comparison of Safety and Immunogenicity of Pediacel™ and Infanrix™ IPV+Hib (Penta) Given in a 3 Dose Schedule in Infants February 2006 September 2008
NCT00290303 Completed Phase 3 Assess if Immune Response of GSK Biologicals' Tritanrix™-HepB/Hib-MenAC Given Without or With Hepatitis B Vaccine at Birth is at Least as Good as Tritanrix™-HepB/Hiberix™ Without Hepatitis B Vaccine at Birth, When Given to Healthy Infants May 2004 March 2005
NCT00290342 Completed Phase 3 Evaluation of the Immunogenicity, Safety and Reactogenicity of the Combined DTPa-IPV Vaccine in Healthy Infants January 1, 2006 January 23, 2007
NCT00291967 Completed Phase 2 Assess Immune Response Following Primary Vaccination With Tritanrix™-HepB Vaccine Mixed With 3 Formulations of Hib-MenAC Vaccine to Infants November 2002
NCT00297856 Completed Post-marketing Safety Study of GSK Biologicals' Boostrix® Vaccine March 2006 December 2006
NCT00303316 Completed Phase 3 Immunogenicity Study of Antibody Persistence and Booster Effect of PENTAXIM™ at 18 Months in Healthy Argentinean Infants February 2006 September 2007
NCT00304265 Completed Phase 4 Post-marketing Evaluation of Reactions Following Receipt of Recommended Adolescent Pertussis Vaccine March 2006 October 2007
NCT00307567 Completed Phase 2 Multicentre Booster & Immune Memory Study of a Booster Dose of GSK Biologicals' 10-valent Pneumococcal Conjugate Vaccine or a Single Dose of 23-valent Plain Polysaccharide Vaccine in Healthy Children Aged 11-18 Mths, Previously Vaccinated in Study 103488 November 2005 March 2006
NCT00313911 Completed Phase 3 Safety of DTaP-IPV-Hep B-PRP~T Combined Vaccine Compared to Tritanrix-HepB/Hib™ and OPV Given at Age 2, 4, and 6 Months. July 2006 February 2008
NCT00316147 Completed Phase 3 Immunogenicity & Safety of GSK's Combined DTPa-HBV-IPV/Hib Vaccine in Indian Infants at 2 Diff Vaccination Schedules December 2005 August 2006
NCT00317135 Completed Phase 3 Safety Study of a Vaccine Against Meningitis in Infants ( 2,4 & 6 Months Age) After a Birth Dose of Hepatitis B. December 11, 2003 October 23, 2004
NCT00317161 Completed Phase 3 Immunogenicity & Safety Study of a Vaccine Against Meningitis in Infants (2,4,6 Months) After a Hepatitis B Birth Dose. August 2004 April 2005
NCT00317174 Completed Phase 2 A Study to Assess Antibody Persistence, Boostability & Safety in Previously Primed Subjects. July 2003 April 2004
NCT00317187 Completed Phase 3 Safety Study of a Vaccine Against Meningitis in Infants (2,4 & 6 Months Age) After a Birth Dose of Hepatitis B. June 8, 2004 January 16, 2005
NCT00319553 Completed Phase 4 Post-licensure, Modified Double-blind, Multi-center Study Evaluating Safety and Immunogenicity of ADACEL® and BOOSTRIX® May 2006 December 2008
NCT00319852 Completed Phase 3 Immunogenicity and Safety of Tetraxim Versus Local DTP + IPV April 2006 July 2008
NCT00320463 Completed Phase 3 Compare Immunogenicity & Safety of 2 Formulations of GSK Biologicals' DTPa-HBV-IPV/Hib Vaccine Given in Healthy Infants April 2006 January 2007
NCT00325130 Completed Phase 3 Concomitant Use of Gardasil (V501) (Human Papillomavirus [Types 6, 11, 16, 18] Recombinant Vaccine) With Combined Diphtheria, Tetanus, Pertussis Vaccine and Meningococcal Conjugate Vaccine in Adolescents (V501-025) April 2006 April 2007
NCT00325143 Completed Phase 3 Safety of DTPa-IPV/Hib & DTPa-HBV-IPV/Hib, Followed by DTPa-IPV/Hib Vaccine in Infants Who Received Hepatitis B Vaccine December 1, 2003 February 1, 2007
NCT00325156 Completed Phase 4 Assess the Safety & Reactogenicity of DTPa-IPV/Hib Vaccine Administered at 3, 4, 5 & 18 Mths of Age, in Healthy Infants November 2, 2004 August 23, 2007
NCT00332566 Completed Phase 3 Assess Immunogenicity, Reactogenicity, Safety of a Booster of GSK Biologicals DTPw-HBV/Hib Kft Compared to DTPw-HBV/Hib June 2006 October 2006
NCT00337428 Completed Phase 3 Concomitant Use of Gardasil (V501, Human Papillomavirus [Types 6, 11, 16, 18] Recombinant Vaccine) With Combined Diptheria, Tetanus, Pertussis and Poliomyelitis Vaccine in Adolescents (V501-024)(COMPLETED) May 2006 May 2007
NCT00343421 Completed Phase 3 Study to Compare Pediacel® to Infanrix®-IPV+Hib When Both Are Co-Administered With Prevenar® in Infants and Toddlers July 2006 June 2009
NCT00343889 Completed Phase 3 Comparison of DTaP-HB-PRP~T Combined Vaccine to Tritanrix-HepB/Hib™, Both Given Concomitantly With Oral Polio Vaccine August 2006 April 2008
NCT00346073 Completed Phase 3 Safety and Immunogenicity of GSK's Tdap Vaccine (Boostrix) in Adults Aged 19 to 64 Years July 13, 2006 March 7, 2007
NCT00347958 Completed Phase 4 Descriptive, Open-label, Multicenter Study of the Safety of Redosing With ADACEL® Vaccine August 2006 October 2008
NCT00348881 Completed Phase 3 Study Comparing a DTaP-HB-PRP~T Combined Vaccine With Tritanrix HepB/Hib™, Concomitantly With OPV in Healthy Infants June 2006 June 2008
NCT00352963 Completed Phase 3 Immunogenicity & Safety Study of Combined/Separate Vaccine(s) Against Common Diseases in Infants (2,4,6 Months of Age). September 30, 2003 July 16, 2004
NCT00355121 Completed Phase 2 Study of Menactra® in Children Aged 4 to 6 Years When Administered Concomitantly With a Fifth Dose of DAPTACEL® October 2006 July 2009
NCT00362427 Completed Phase 2 Study of PR5I, a Pediatric Combination Vaccine With Enhanced Hepatitis B Component Given Concomitantly With Prevnar® August 2006 March 2009
NCT00376779 Completed Phase 2 Immunogenicity and Safety of a DTPa-HBV-IPV/Hib Vaccine Given at 2, 3 and 4 Months of Age October 2006 May 2007
NCT00379977 Completed Phase 3 Study to Assess the Safety & Reactogenicity of GSK Biologicals' DTPa/Hib Vaccine When Given at 3, 4 and 5 Months of Age September 2006 December 2006
NCT00385255 Completed Phase 3 Immunogenicity, Safety of GSKs Tdap Vaccine Boostrix When Coadministered With GSKs Influenza Vaccine Fluarix in Adults October 23, 2006 February 28, 2007
NCT00404651 Completed Phase 3 Lot Consistency Study of DTaP-IPV-HB-PRP~T Vaccine Administered at 2-4-6 Months of Age in Healthy Infants November 2006 July 2008
NCT00406562 Completed Phase 3 Study to Assess the Safety & Reactogenicity of GSK Biologicals' dTpa Vaccine (Boostrix) When Given at 6-8 Years of Age. January 2007 February 2007
NCT00412854 Completed Phase 3 Study to Assess Safety & Immunogenicity of GSK Biologicals' DTPa/Hib Vaccine vs Separate Administration of DTPa and Hib. January 3, 2007 June 25, 2007
NCT00432042 Completed Phase 3 Immunogenicity and Safety Study of Proquad® and Infanrix® Hexa When Administered Concomitantly (V221-035) January 12, 2007 March 27, 2008
NCT00447525 Completed Phase 3 REVAXIS® Versus DT Polio® as a Second Booster in 6 Year-old Children February 2007 January 2008
NCT00452686 Completed Phase 3 Study to Assess Safety & Immunogenicity of GSK Biologicals' Boostrix (dTpa) Vaccine vs. Chinese DT Vaccine March 2007 May 2007
NCT00453570 Completed Phase 3 Immunogenicity and Safety of Pentaxim as 3 Doses Primary Vaccination Followed by a Booster Dose at 18 Months March 2007 January 2009
NCT00457249 Completed Phase 4 A Trial to Evaluate the Safety and Immunogenicity of ADACEL® Vaccine in Persons 65 Years of Age and Older March 2007 November 2008
NCT00463437 Completed Phase 3 Pneumococcal Vaccine Booster Study in Healthy Children 11-18 Months Old Previously Primed With the Same Vaccines April 25, 2007 June 14, 2008
NCT00467519 Completed Phase 3 Safety and Immunogenicity of Tdap Vaccine Compared to DTaP Vaccine in Children 4 to 6 Years of Age April 2007 December 2009
NCT00473668 Completed Phase 3 Non-inferiority of GSK Biologicals' DTPw-HBV/Hib Compared to Two Formulations of GSK Biologicals' DTPw-HBV/Hib June 1, 2007 January 30, 2008
NCT00489970 Completed Phase 3 Persistence Study of GSK Biologicals' Tdap Vaccine 1, 3, 5 and 9 Years Following Administration as an Initial Single Dose in Healthy Young Adults and to Evaluate the Immunogenicity and Safety of Boostrix as a Second Dose of Tdap, When Administered at Year 9 June 1, 2007 March 1, 2016
NCT00514059 Completed Phase 4 Immunogenicity and Safety Study of a Booster Dose (5th) of Diphteria-Tetanus-Pertussis-Polio Vaccine April 2007 June 2007
NCT00514709 Completed Phase 3 Immunogenicity Study of Antibody Persistence and Booster Effect of DTaP-HB PRP~T Combined Vaccine in Filipino Infants September 2007 April 2009
NCT00518180 Completed Phase 3 A Study to Evaluate Safety and Immune Response of Novartis Meningococcal ACWY Conjugate Vaccine In Adolescents July 2007 October 2008
NCT00534833 Completed Phase 3 Immunogenicity Study of Antibody Persistence and Booster Effect of DTaP-HB-PRP~T Combined Vaccine or Tritanrix-HepB/Hib™ September 2007 March 2009
NCT00548171 Completed Phase 4 Immunogenicity & Reactogenicity of Boostrix 10 Years After Previous Booster Vaccination in Study NCT01267058 November 5, 2007 April 30, 2008
NCT00601835 Completed Phase 4 Canadian Manufactured Tetanus and Diphtheria Toxoids Adsorbed (Td) Vaccine Compared With U.S. Manufactured Td May 2004 July 2005
NCT00610168 Completed Phase 4 Immunogenicity & Reactogenicity of Boostrix 10 Years After Previous Booster Vaccination. January 1, 2008 April 30, 2008
NCT00611559 Completed Phase 4 Study of a New Formulation of DTPa-HBV-IPV/Hib Vaccine Administered as a Booster Dose to 18-23 Months Old Children February 14, 2008 June 25, 2008
NCT00617812 Completed Phase 4 Safety and Immunogenicity Study of a Liquid Pentavalent Combination Vaccine March 2008 May 2009
NCT00627458 Completed Phase 2 Immunogenicity and Reactogenicity of a Booster Dose of GSK Bio's DTPa-HBV-IPV/Hib Vaccine February 1, 2008 August 18, 2008
NCT00635128 Completed Phase 4 Safety and Immunogenicity of a Booster Dose of GSK Biological's Boostrix-Polio Vaccine February 1, 2008 July 8, 2008
NCT00654901 Completed Phase 3 Study of the DTaP-IPV-Hep B-PRP~T Combined Vaccine Following a Primary Series of DTacP IPV-HepB-PRP-T or Infanrix Hexa™ March 2008 July 2009
NCT00662870 Completed Phase 3 Study of the Safety, Immunogenicity and Lot Comparability of DAPTACEL When Administered With Other Recommended Vaccine May 2001 January 2004
NCT00674908 Completed Phase 4 Phase IV Interchangeability Study of a Liquid Pentavalent Combination Vaccine March 2008 May 2009
NCT00696423 Completed Phase 3 Immunogenicity and Safety of GSK Biologicals' Infanrix/Hib in Children June 7, 2008 July 26, 2008
NCT00707148 Completed Phase 1 Pertussis Vaccine in Healthy Pregnant Women January 2009 May 2012
NCT00712959 Completed Phase 4 Immune Responses in Adults to Revaccination With ADACEL® 10 Years After a Previous Dose June 2008 December 2009
NCT00753649 Completed Phase 4 Immunogenicity and Safety of GSK Biologicals' Infanrix Hexa in Infants September 23, 2008 March 12, 2013
NCT00772369 Completed Retrospective Survey of Safety of Fourth Dose Pentacel® in Children September 2003 April 2005
NCT00772928 Completed Phase 3 Study of the Effect of Pneumococcal Conjugate Vaccine (PCV) on Immunogenicity of Pentacel™ October 2003 November 2006
NCT00777257 Completed Phase 4 Study of Menactra® in US Adolescents When Administered Concomitantly With Tdap Vaccine April 2005 September 2007
NCT00797511 Completed Phase 3 Immunogenicity and Safety of Adacel Polio Vaccine November 2008 July 2009
NCT00802867 Completed Phase 4 Study of DAPTACEL® Administered as a 5th Dose in 4 to 6-Year-Old Children Previously Immunized With PENTACEL™ February 2004 September 2005
NCT00804284 Completed Database Surveillance Safety Study of PENTACEL® Vaccine September 2008 January 2015
NCT00831311 Completed Phase 2 Study of DTaP-IPV-Hep B-PRP~T Combined Vaccine Compared With PENTAXIM™ and ENGERIX B® PEDIATRICO in Argentinean Infants October 2004 March 2007
NCT00831753 Completed Phase 3 Study of DTaP-IPV-Hep B-PRP~T Combined Vaccine Compared to Infanrix®Hexa in Healthy Peruvian Infants May 2008 November 2009
NCT00835237 Completed Phase 3 Evaluation of GlaxoSmithKline Biologicals' Boostrix® Vaccine in Comparison With Decavac™ Vaccine. February 17, 2009 October 15, 2009
NCT00855855 Completed Surveillance Program to Determine Product Specific Rates of Invasive Hib Disease February 2009 December 2014
NCT06302374 Completed Phase 1/Phase 2 Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Immunogenicity of GR2001 in Chinese Healthy Adults March 4, 2023 February 19, 2024
NCT00109330 Completed Phase 3 A Combined Tdap Vaccine Used As A Booster Compared To Licensed Td Vaccine November 2002 April 2004
NCT00133445 Completed Phase 2 Pentavalent DTaP-Hep B-IPV December 2005 August 2006
NCT02569879 Completed Impact of Boostrix™ Maternal Vaccination on Morbidity and Mortality of Pertussis Disease in Infants ≤6 Weeks of Age, in Bogota, Colombia. October 1, 2015 April 14, 2018
NCT02587520 Completed Phase 1/Phase 2 Study of Tetanus Toxoid, Reduced Diphtheria Toxoid, and Acellular Pertussis Vaccine Adsorbed in Healthy Subjects October 22, 2015 February 21, 2017
NCT02817451 Completed Phase 3 DTaP-IPV-HB-PRP-T Combined Vaccine as a Primary Series and a Second Year of Life Booster in HIV-Exposed Infected and Uninfected Infants July 14, 2016 February 22, 2019
NCT02853929 Completed Phase 4 Evaluation of Immunogenicity and Safety of a Booster Dose of Infanrix Hexa™ in Healthy Infants Born to Mothers Vaccinated With Boostrix™ During Pregnancy or Immediately Post-delivery September 19, 2016 March 19, 2019
NCT02858440 Completed Phase 3 A Study to Assess the Immunogenicity and Safety of GSK Biologicals' Infanrix-IPV/Hib Vaccine Administered as a Three-dose Vaccination Course at 3, 4.5 and 6 Months of Age and a Booster Dose at 18 Months of Age in Healthy Infants in Russia September 13, 2016 November 13, 2018
NCT02999815 Completed Phase 1/Phase 2 Intrathecal Tetanus Immunoglobulin to Treat Tetanus February 13, 2017 May 1, 2020
NCT03208101 Completed Phase 1 A Study to Compare LBVD to Eupenta and Imovax Polio in Healthy Adults July 3, 2017 December 21, 2017
NCT03266211 Completed Antitetanus Vaccination for People Older Than 65 Years. November 9, 2017 December 23, 2017
NCT03552445 Completed Phase 4 Immunogenicity and Safety of a Tetanus-diphtheria Vaccine and a 13-valent Pneumococcal Conjugate Vaccine November 1, 2013 February 28, 2018
NCT03589768 Completed Phase 2 Study on the Safety and Immunogenicity of Boostrix Vaccine in Pregnant Malian Women and Their Infants January 24, 2019 July 1, 2020
NCT03870061 Completed N/A Evaluation of an Infant Immunization Encouragement Program in Nigeria July 1, 2018 February 20, 2020
NCT03891758 Completed Phase 3 Confirmatory Study of BK1310 in Healthy Infants April 1, 2019 August 10, 2020
NCT03931239 Completed N/A The Transparent Safety Study of the 5 in 1 (DTwP-rHepB-Hib) Combination Vaccine Produced by the Indian Serine Institute in Children of Viet Nam Healthy From 6 to 12 Weeks of Age in a 3-dose Regimen, the Interval Between Doses is 4 Weeks March 1, 2018 July 30, 2018
NCT03950986 Completed N/A Increasing Vaccine Uptake Among Veterans at the Atlanta VA Health Care System October 15, 2018 June 30, 2019
NCT04099303 Completed Phase 1 Phase I Clinical Trial of Diphtheria, Tetanus and Acellular Pertussis (Three Components) Combined Vaccine, Adsorbed . April 28, 2020 November 25, 2021
NCT04142983 Completed Phase 2/Phase 3 Tdap Vaccine Safety for Plasma Donors February 3, 2020 November 16, 2021
NCT04165928 Completed Multicenter Study of Tetanus Patients in Fujian Province of China July 1, 2018 October 31, 2019
NCT04177485 Completed N/A Evaluating a Caregiver SMS Reminder Intervention to Reduce Immunization Drop-out in Arua, Uganda February 1, 2016 December 4, 2017
NCT04618939 Completed Phase 3 To Evaluate the Immunogenicity and Safety of 'BR-TD-1001' Administered Intramuscularly in Healthy Children October 20, 2016 April 28, 2017
NCT05625477 Completed Phase 2 Study to Compare the Anti-tetanus Neutralizing Antibody Titers and Safety of TNM002 Injection With Human Tetanus Immunoglobulin or Placebo in Adult Volunteers April 18, 2022 October 18, 2022
NCT05664750 Completed Phase 3 Study to Compare the Efficacy and Safety of Passive Immunization With TNM002 Injection and Human Tetanus Immunoglobulin as Prophylaxis Against Tetanus December 22, 2022 July 7, 2023
NCT06034093 Completed N/A Real-time Artificial Intelligent (AI)-Assisted Muscle Ultrasound for Monitoring Muscle Mass Reduction in ICU Patients June 1, 2020 October 31, 2023
NCT00092469 Completed Phase 3 Study of an Investigational Vaccine in Healthy Infants in Taiwan (V441-001)(COMPLETED) March 2002 August 2003
NCT00871000 Completed Phase 3 Immunogenicity and Safety of Boostrix Polio Vaccine as a Booster Dose in 5 to 6-year-old Children. April 1, 2009 November 18, 2009
NCT00871117 Completed Phase 3 Immunogenicity and Safety of Kinrix + (Measles Mumps Rubella) MMR Vaccine With and Without Varicella Vaccine in Healthy Children 4-6 Years March 31, 2009 June 15, 2010
NCT00879827 Completed Phase 3 Immunogenicity and Reactogenicity of GSK Bio DTPa-HBV-IPV and Hib Vaccines When Coadministered to Healthy Infants September 2000 May 2001
NCT00908115 Completed Post Market Surveillance for Infanrix™ August 1, 2003 June 23, 2008
NCT00964028 Completed Phase 3 Safety Study of GSK Biologicals' DTPa-IPV/Hib (Infanrix™-IPV/Hib) December 1, 2009 April 12, 2010
NCT00970307 Completed Phase 2 Immunogenicity and Safety Study of GSK Biologicals' GSK2202083A Vaccine in Healthy Infants at 2, 3 and 4 Months of Age August 13, 2009 January 27, 2010
NCT01031303 Completed Phase 4 Immunogenicity and Safety of TETRAXIM™ Given as a Booster Dose at 4 to 6 Years of Age December 2009 January 2011
NCT01040052 Completed Phase 3 A Study to Assess the Safety of Adacel® Vaccine December 2009 April 2010
NCT01062477 Completed Phase 3 A Study of DTaP//PRP-T Combined Vaccine (ACTACEL) Versus Local DTaP and Act-HIB Monovalent Vaccine in Healthy Infants January 2010 December 2011
NCT01086423 Completed Phase 3 Immunogenicity and Safety Study of GSK Biologicals' Infanrix-IPV+Hib™ Vaccine March 1, 2010 November 19, 2010
NCT01090453 Completed Phase 2 Study of GlaxoSmithKline Biologicals' GSK2202083A Vaccine in Healthy Infants May 17, 2010 October 11, 2011
NCT01105559 Completed Antibody Persistence in Healthy Children After Primary and Booster DTaP-IPV-Hep B-PRP-T Vaccine or Control Vaccine April 2010 December 2011
NCT01106092 Completed Phase 2 Study to Evaluate the Immunogenicity and Reactogenicity of a Booster Dose of GSK2036874A Vaccine in Healthy Toddlers May 13, 2010 September 2, 2010
NCT01137435 Completed Phase 4 Post Marketing Surveillance for ADACEL™ in South Korea June 2010 September 2016
NCT01147900 Completed Phase 4 Evaluation of Boostrix™10 Years After Previous Booster Vaccination June 15, 2010 May 8, 2012
NCT01171989 Completed Phase 2 Immunogenicity and Safety Study of GlaxoSmithKline Biologicals' GSK2202083A Vaccine Administered as a Booster Dose August 18, 2010 December 3, 2010
NCT01177722 Completed Phase 3 A Study of DTaP-IPV-Hep B-PRP-T Vaccine Given With Prevenar™ and Rotarix™ in Healthy Latin American Infants August 2010 December 2011
NCT01214889 Completed Phase 3 Study of PENTAXIM™ Vaccine Versus TETRAXIM™ Vaccine Given With ACTHIB™ Vaccine in South Korean Infants. September 2010 December 2011
NCT01245049 Completed Phase 3 Immunogenicity and Safety of GSK Biologicals' Boostrix Polio Vaccine in 3 and 4-year-old Children April 1, 2011 April 2, 2012
NCT01248884 Completed Phase 2 Safety and Immunogenicity of New Formulations of GlaxoSmithKline Biologicals' DTPa-HBV-IPV/Hib Vaccine (GSK217744) December 9, 2010 January 5, 2012
NCT01249183 Completed Phase 3 Safety and Immunogenicity Study of Concomitant Versus Non Concomitant Administration of a Diphtheria, Tetanus, Pertussis and Poliomyelitis Vaccine (REPEVAX) and Influenza Vaccine (VAXIGRIP) in Subjects Aged From 60 Years Old October 2010 September 2011
NCT01267058 Completed Phase 3 Booster Study of Combined Diphtheria-tetanus-acellular Pertussis Vaccine in Healthy Adults September 1997 February 1998
NCT01277705 Completed Phase 3 Comparison of GSK Biologicals' Reduced Antigen Diphtheria and Tetanus Toxoids and Acellular Pertussis- Inactivated Poliovirus Vaccine, to BoostrixTM and Inactivated Poliovirus Vaccine Administered Separately and With Revaxis® January 2002 April 2002
NCT01287949 Completed Phase 3 Safety and Immunogenicity Study of a Diphtheria, Tetanus, Acellular Pertussis and Poliomyelitis Vaccine (REPEVAX) Followed by 2 Doses of a Diphtheria, Tetanus and Poliomyelitis Vaccine (REVAXIS) in Subjects of 40 Years of Age or Older January 2011 May 2012
NCT01294605 Completed Phase 4 Immunogenicity and Reactogenicity Study of BoostrixTM (dTpa) and Boostrix-IPV (dTpa-IPV) April 2003 September 2004
NCT01309646 Completed Phase 3 Immunogenicity and Safety of GlaxoSmithKline Biologicals' Infanrix™-IPV+Hib Vaccine March 4, 2011 February 24, 2012
NCT01311557 Completed Phase 4 Study of Adacel® Vaccine Administered to Persons 10 Years of Age March 2011 January 2012
NCT01323959 Completed Phase 4 Immunogenicity and Safety of Booster Dose of BoostrixTM Polio Vaccine in Previously Boosted Adults April 1, 2011 March 1, 2012
NCT01331252 Completed N/A Pneumonia in Tetanus Study August 2000 March 2002
NCT01338688 Completed The Change of the Tetanus Antibody Titer After Single Injection of Td and Simultaneous Injection of TIG With Td October 2008 October 2010
NCT01346293 Completed Phase 3 Study of DTap-IPV Compared to DAPTACEL® and IPOL® as the 5th Dose in Children 4 to 6 Years of Age April 2011 September 2013
NCT01353703 Completed Phase 3 Immunogenicity and Safety Study in Infants of GlaxoSmithKline Biologicals' Infanrix Hexa™ (DTPa-HBV-IPV/Hib) Vaccine April 16, 2012 February 25, 2013
NCT01357720 Completed Phase 4 Study to Assess if Quinvaxem Can be Interchanged With Other Pentavalent Vaccines During Standard Childhood Vaccination May 2011 September 2011
NCT01358825 Completed Phase 4 Study to Evaluate Antibody Persistence in Children Previously Vaccinated With Infanrix Hexa™ or Infanrix-IPV/Hib™ May 30, 2011 July 15, 2011
NCT01362322 Completed Phase 4 Immunogenicity and Safety of BoostrixTM Using a New Syringe in 10 to 15-year Old Adolescents July 1, 2011 September 3, 2012
NCT01362517 Completed Phase 3 Study of Quinvaxem for Vaccination Against Diphtheria, Pertussis, Tetanus, Hepatitis B and Diseases Caused by Haemophilus Influenzae Type B April 2010 April 2011
NCT01437423 Completed Phase 4 Regulatory Post-Marketing Surveillance Study for TETRAXIM™ June 2011 November 2015
NCT01439165 Completed Phase 4 Safety and Immunogenicity in Adults of Revaccination With Adacel® Vaccine 10 Years After a Previous Dose November 2011 February 2017
NCT01444781 Completed Phase 3 Study of the Booster Effect of DTaP-IPV-Hep B-PRP~T Combined Vaccine or Infanrix Hexa™ and Prevenar™ in Healthy Infants September 2011 October 2013
NCT01449812 Completed Phase 3 Immunogenicity and Safety Study of Booster Dose of GSK Biologicals' IPV (Poliorix™) and DTPa/Hib (Infanrix+Hib™) Vaccine October 1, 2011 January 16, 2012
NCT01453998 Completed Phase 2 Safety and Immunogenicity of a Booster Dose of New Formulations of GlaxoSmithKline Biologicals' DTPa-HBV-IPV/Hib Vaccine (GSK217744) October 14, 2011 November 12, 2012
NCT01457495 Completed Phase 2 Immunogenicity and Safety of DTPa-HBV-IPV/Hib Compared to DTPa-IPV/Hib and HBV Administered Concomitantly September 1998 September 1999
NCT01457508 Completed Phase 3 Immunogenicity and Reactogenicity of DTPa-HBV-IPV/Hib, Compared to DTPa-HBV-IPV and Hib Administered Separately January 1999 March 2000
NCT01457547 Completed Phase 4 Comparison of Immunogenicity and Reactogenicity of INFANRIX™ HEXA and HEXAVAC™ Vaccines as a Primary Vaccination Course October 2003 May 2005
NCT01457560 Completed Phase 3 Immunogenicity and Reactogenicity of DTPa-HBV-IPV/Hib Vaccine Followed by the Same Vaccine and Oral Polio Vaccine February 2000 April 2001
NCT01470287 Completed Phase 3 Immunogenicity, Safety and Tolerability of a Fully Liquid Pentavalent (DTwP-Hib-Hep B) Vaccine in Infants 6-8 Weeks of Age December 2011 April 2012
NCT01491087 Completed Phase 4 Safety of PENTAXIM® Given as a Three-Dose Primary Vaccination at 2, 3, and 4 Months of Age in Infants in China December 2011 December 2012
NCT01529645 Completed Phase 1 Safety and Dose Ranging Study of Acellular Pertussis and Acellular Pertussis -Tetanus-Diphtheria Booster Vaccines in Healthy Adults Ages 18 to 40 Years March 2012 July 2013
NCT01546909 Completed Phase 4 Antibody Persistence to REVAXIS or DT Polio and Immune Response to TETRAVAC-ACELLULAIRE February 2012 December 2012
NCT01559597 Completed N/A Comparative Study of Two Tetanus Toxoid Vaccination Strategies: Cold Chain Versus Controlled Temperature Chain November 2012 March 2013
NCT01568060 Completed Post-marketing Surveillance to Assess the Safety of Infanrix-IPV Vaccine Among Infants and Children in Korea May 21, 2012 December 15, 2015
NCT01577732 Completed Phase 3 Safety of GSK Biologicals' Infanrix-IPV+HibTM Vaccine in Healthy Vietnamese Toddlers December 8, 2012 April 9, 2013
NCT01629589 Completed Phase 4 Immunogenicity of Adacel® and BOOSTRIX® Vaccines in Adolescents June 2012 June 2013
NCT01659996 Completed Phase 4 Study of Menactra® in Healthy Subjects at 9 Months and Concomitantly With Pentacel® at 15 to 18 Months of Age July 2012 September 2015
NCT01689324 Completed Phase 1/Phase 2 Study of Tetanus Toxoid, Reduced Diphtheria Toxoid and Acellular Pertussis Vaccine (ADACEL®) as a Booster in Adolescents September 2012 May 2013
NCT01711645 Completed Phase 4 Tdap Vaccine in Post-Partum Women October 26, 2012 August 28, 2015
NCT01738477 Completed Phase 3 Immunogenicity and Safety of GlaxoSmithKline (GSK) Biologicals' Boostrix™ Vaccine in Previously Boosted Young Adults January 31, 2013 April 2, 2014
NCT01878435 Completed N/A Randomized Controlled Trial of the Impact of Mobile Phone Delivered Reminders and Travel Subsidies to Improve Childhood Immunization Coverage Rates and Timeliness in Western Kenya October 2013 February 2016
NCT01890850 Completed Study to Analyze the Risk Factors Associated With Pertussis/Whooping Cough Infection Among Infants July 2013 November 2013
NCT01917357 Completed Phase 3 A Comparison of the Immunogenicity and Safety of Quinvaxem in Mono-dose Vials and Uniject September 2013 April 2014
NCT01933776 Completed Phase 1 Study of the Tdap Combined Vaccine (ADACEL™) as a Booster Dose in Healthy Adults and Children in China August 2013 January 2014
NCT01948193 Completed Phase 3 Study of DTaP-IPV-Hep B-PRP~T Combined Vaccine in Indian Infants Previously Given a Dose of Hepatitis B Vaccine at Birth February 2014 June 2015
NCT01983540 Completed Phase 3 Antibody Persistence at Age 3.5 and 4.5 Years After Primary and Booster DTaP-IPV-Hep B-PRP~T or Infanrix Hexa Vaccination October 2013 December 2015
NCT01988857 Completed Phase 3 Safety of a Booster Dose of GlaxoSmithKline (GSK) Biologicals' Boostrix™ Vaccine in Healthy Vietnamese Children February 22, 2014 May 10, 2014
NCT01993173 Completed Phase 3 Sanofi Pasteur's Tdap Combined Vaccine as a Booster Versus Local DT Vaccine in Children or Versus Local Td Vaccine in Adolescents and Adults in China. November 2013 April 2015
NCT02040636 Completed Phase 2 Study of Tetanus and Diphtheria Toxoids Adsorbed Combined With Component Pertussis Vaccine and Inactivated Poliomyelitis January 1999 May 2000
NCT02089347 Completed Phase 3 Study of SP306 Given Intramuscularly Compared to DT Given Subcutaneously in Japanese Adolescents 11 - 12 Years Old March 2014 March 2015
NCT02094833 Completed Phase 3 DTaP-IPV-Hep B-PRP~T Combined Vaccine Versus DTaP-IPV//PRP~T Combined Vaccine + Hep B Vaccine in Hep B Primed Infants March 2014 November 2016
NCT02096263 Completed Phase 3 Study to Determine the Immunogenicity and Safety of GlaxoSmithKline (GSK) Biologicals; Infanrix Hexa at 2, 4 and 6 Months of Age in Healthy Infants April 16, 2014 November 13, 2015
NCT02118961 Completed Phase 3 Study of BK1301 (DTaP Vaccine) as a Booster in Adolescents April 2014 August 2014
NCT02274285 Completed Phase 3 DTaP-IPV/Hib Vaccine Primary & Booster Vaccinations Versus Co-administration of DTaP-IPV and Hib Vaccine in Japanese Infants October 2014 May 28, 2016
NCT02422264 Completed Phase 4 Immunogenicity and Safety Study of Infanrix Hexa in Healthy Infants Born to Mothers Vaccinated With Boostrix™ During Pregnancy or Immediately Post-delivery January 22, 2016 March 7, 2018
NCT02428491 Completed Phase 3 Immunogenicity and Safety of Sanofi Pasteur's Combined Vaccine Given as a Three-Dose Primary Series at 2, 3,4 Months of Age and Followed by a Booster Dose Given at 16 to 17 Months of Age in Vietnamese Infants Who Previously Received a Dose of Hepatitis B Vaccine at Birth or Within 1 Week After Birth April 20, 2015 January 11, 2017
NCT02447978 Completed Duration of Protection: GSK DTaP Vaccines February 2015 June 2015
NCT02458183 Completed Phase 3 Vaccine -diphthEria -tetaNus -Acellular pertUssis-inactivated polioviruS February 2, 2015 May 5, 2018
NCT02538211 Completed N/A The Role of the Intestinal Microbiome in Enteric and Systemic Vaccine Immune Responses September 2015 February 2017
NCT05457946 Not yet recruiting Phase 2/Phase 3 Study to Evaluate the Immunogenicity and Safety of LBVD(Hexavalent Vaccine), Given to Healthy Infants at Primary Series April 1, 2023 September 30, 2025
NCT05952596 Not yet recruiting Phase 1 A Study to Evaluate Safety and Immunogenicity of APV006 in Healthy Adults July 17, 2023 March 31, 2024
NCT06056050 Recruiting Phase 1 A Clinical Trial of Adsorbed Cell-free DPT Vaccine (5-component) (for People Aged 6 Years and Above) December 6, 2023 February 28, 2025
NCT06049940 Recruiting Phase 3 Safety and Immunogenicity of Tetanus Vaccine, Adsorbed in 18~44 Years Old Population September 1, 2023 March 30, 2025
NCT06184542 Recruiting Phase 1 Phase I Clinical Trial of Diphtheria-Tetanus-acellular Pertussis Component Combined Vaccine December 23, 2023 November 1, 2026
NCT06120751 Recruiting Phase 3 A Clinical Trial to Evaluate the Safety and Immunogenicity of a Single Dose of Adsorbed Tetanus Vaccine in a Population Aged 18 Years and Over March 20, 2024 July 2024
NCT00316680 Terminated Phase 3 Immuno & Safety Study With 2 Formulations of DTPw-HBV/HIB When Given at Birth With Hepatitis B at 2, 4 and 6 Mths.Age. March 2006 November 2006
NCT00871741 Terminated Phase 2 Feasibility Study of GlaxoSmithKline Biologicals' GSK2202083A Vaccine in Healthy Infants at 3, 5 and 11 Months of Age. April 1, 2009 June 25, 2009
NCT00544271 Terminated Phase 4 Immunogenicity, Antibody Persistence and Safety of GSK Biologicals' DTPa (INFANRIX) and dTpa (BOOSTRIX) Vaccines. May 2003 January 2004
NCT00437671 Terminated Phase 4 Tetanus Immunization in Subjects With No Immunization History or With Tetanus Antibody Levels Below Protective Levels March 2007 September 2007
NCT02257645 Unknown status Post-authorization Safety Study of Euforvac-Hib Vaccine for Active Primary Immunization in Infants From 6 Weeks March 2015 September 2016
NCT03341195 Unknown status N/A Mobile Phone SMS Messages and Automated Calls in Improving Vaccine Coverage Among Children in Pakistan January 2018 September 2018
NCT04618640 Unknown status Phase 3 To Evaluate the Immunogenicity and Safety of DTaP-IPV Vaccine Administered as a Boosting Dose to Healthy Children of 4-6 Years December 26, 2019 July 30, 2021
NCT00877357 Unknown status Phase 4 Safety, Long Term Immunogenicity and Lot Consistency Study of Liquid Pentavalent Combination Vaccine January 2009 February 2013
NCT00932269 Unknown status Seroimmunity 2007 and Sub Study of the Swedish Population Regarding Vaccine Preventable Disease March 2007 September 2011
NCT04056728 Unknown status Phase 4 A Phase IV Study to Assess the Safety of EupentaTM Inj September 23, 2019 December 31, 2020
NCT02813486 Unknown status Phase 1/Phase 2 Safety and Immunogenicity Study of Tetanus, Diphtheria and Acellular Pertussis (Tdap) Vaccine June 2016 November 2016
NCT04073459 Unknown status Phase 2 Safety and Immunogenicity of Hexavalent Vaccine(DTwP-HepB-IPV-Hib) in Healthy Infants November 2019 August 2020
NCT04238975 Unknown status Phase 2 A Study to Evaluate the Safety and Efficacy(Immunogenicity) of GC3111 in Healthy Adults October 14, 2019 May 2021
NCT00870350 Unknown status Phase 4 An Immunogenicity and Safety Study of Tetanus, Diphtheria and Acellular Pertussis Vaccine Booster April 2009 June 2010
NCT01810731 Withdrawn Phase 2/Phase 3 Safety and Immunogenicity Study of Influenza Vaccines in HIV-infected and HIV-uninfected Pregnant Women in Western Kenya April 2014 April 2014
NCT01003431 Withdrawn Phase 3 A Study of the Immunogenicity and Safety of Whole-Cell Pertussis Containing Vaccine Administered Concomitantly With RotaTeq™ (V260) or Rotarix™ (V260-036)(WITHDRAWN) December 2009 September 2010
NCT03128489 Withdrawn Phase 3 Evaluation of Immunogenicity and Safety of DTPa-IPV/Hib Conjugate Vaccine (Infanrix™-IPV/Hib) Administered at 6, 10 and 14 Weeks in Healthy Indian Infants December 1, 2017 August 1, 2018
Disase is a (Disease Ontology)
DOID:0050338
Cross Reference ID (Disease Ontology)
GARD:5144
Cross Reference ID (Disease Ontology)
ICD10CM:A35
Cross Reference ID (Disease Ontology)
ICD9CM:037
Cross Reference ID (Disease Ontology)
MESH:D013742
Cross Reference ID (Disease Ontology)
NCI:C85185
Cross Reference ID (Disease Ontology)
SNOMEDCT_US_2023_03_01:154312006
Cross Reference ID (Disease Ontology)
UMLS_CUI:C0039614
Exact Synonym (Disease Ontology)
clostridial tetanus
Exact Synonym (Disease Ontology)
Infection due to Clostridium tetani
OrphaNumber from OrphaNet (Orphanet)
3299
MeSH unique ID (MeSH (Medical Subject Headings))
D013742