Clinical Trials Directory

Trials / Conditions / Acellular Pertussis

Acellular Pertussis

67 registered clinical trials studyying Acellular Pertussis.

StatusTrialSponsorPhase
WithdrawnEvaluation of Immunogenicity and Safety of DTPa-IPV/Hib Conjugate Vaccine (Infanrix™-IPV/Hib) Administered at
NCT03128489
GlaxoSmithKlinePhase 3
CompletedEvaluation of Immunogenicity and Safety of a Booster Dose of Infanrix Hexa™ in Healthy Infants Born to Mothers
NCT02853929
GlaxoSmithKlinePhase 4
CompletedImmunogenicity and Safety Study of Infanrix Hexa in Healthy Infants Born to Mothers Vaccinated With Boostrix™
NCT02422264
GlaxoSmithKlinePhase 4
CompletedImpact of Boostrix™ Maternal Vaccination on Morbidity and Mortality of Pertussis Disease in Infants ≤6 Weeks o
NCT02569879
GlaxoSmithKline
CompletedDuration of Protection: GSK DTaP Vaccines
NCT02447978
GlaxoSmithKline
CompletedStudy to Determine the Immunogenicity and Safety of GlaxoSmithKline (GSK) Biologicals; Infanrix Hexa at 2, 4 a
NCT02096263
GlaxoSmithKlinePhase 3
CompletedSafety of a Booster Dose of GlaxoSmithKline (GSK) Biologicals' Boostrix™ Vaccine in Healthy Vietnamese Childre
NCT01988857
GlaxoSmithKlinePhase 3
CompletedStudy to Analyze the Risk Factors Associated With Pertussis/Whooping Cough Infection Among Infants
NCT01890850
GlaxoSmithKline
CompletedImmunogenicity and Safety of GlaxoSmithKline (GSK) Biologicals' Boostrix™ Vaccine in Previously Boosted Young
NCT01738477
GlaxoSmithKlinePhase 3
CompletedSafety of GSK Biologicals' Infanrix-IPV+HibTM Vaccine in Healthy Vietnamese Toddlers
NCT01577732
GlaxoSmithKlinePhase 3
CompletedPost-marketing Surveillance to Assess the Safety of Infanrix-IPV Vaccine Among Infants and Children in Korea
NCT01568060
GlaxoSmithKline
CompletedImmunogenicity and Safety Study in Infants of GlaxoSmithKline Biologicals' Infanrix Hexa™ (DTPa-HBV-IPV/Hib) V
NCT01353703
GlaxoSmithKlinePhase 3
CompletedSafety and Immunogenicity of a Booster Dose of New Formulations of GlaxoSmithKline Biologicals' DTPa-HBV-IPV/H
NCT01453998
GlaxoSmithKlinePhase 2
CompletedImmunogenicity and Safety Study of Booster Dose of GSK Biologicals' IPV (Poliorix™) and DTPa/Hib (Infanrix+Hib
NCT01449812
GlaxoSmithKlinePhase 3
CompletedImmunogenicity and Safety of BoostrixTM Using a New Syringe in 10 to 15-year Old Adolescents
NCT01362322
GlaxoSmithKlinePhase 4
CompletedStudy to Evaluate Antibody Persistence in Children Previously Vaccinated With Infanrix Hexa™ or Infanrix-IPV/H
NCT01358825
GlaxoSmithKlinePhase 4
CompletedImmunogenicity and Safety of GSK Biologicals' Boostrix Polio Vaccine in 3 and 4-year-old Children
NCT01245049
GlaxoSmithKlinePhase 3
CompletedImmunogenicity and Safety of Booster Dose of BoostrixTM Polio Vaccine in Previously Boosted Adults
NCT01323959
GlaxoSmithKlinePhase 4
CompletedImmunogenicity and Safety of GlaxoSmithKline Biologicals' Infanrix™-IPV+Hib Vaccine
NCT01309646
GlaxoSmithKlinePhase 3
CompletedSafety and Immunogenicity of New Formulations of GlaxoSmithKline Biologicals' DTPa-HBV-IPV/Hib Vaccine (GSK217
NCT01248884
GlaxoSmithKlinePhase 2
CompletedImmunogenicity and Safety Study of GlaxoSmithKline Biologicals' GSK2202083A Vaccine Administered as a Booster
NCT01171989
GlaxoSmithKlinePhase 2
CompletedEvaluation of Boostrix™10 Years After Previous Booster Vaccination
NCT01147900
GlaxoSmithKlinePhase 4
CompletedStudy of GlaxoSmithKline Biologicals' GSK2202083A Vaccine in Healthy Infants
NCT01090453
GlaxoSmithKlinePhase 2
CompletedImmunogenicity and Safety Study of GSK Biologicals' Infanrix-IPV+Hib™ Vaccine
NCT01086423
GlaxoSmithKlinePhase 3
CompletedSafety Study of GSK Biologicals' DTPa-IPV/Hib (Infanrix™-IPV/Hib)
NCT00964028
GlaxoSmithKlinePhase 3
CompletedImmunogenicity and Safety Study of GSK Biologicals' GSK2202083A Vaccine in Healthy Infants at 2, 3 and 4 Month
NCT00970307
GlaxoSmithKlinePhase 2
CompletedImmunogenicity and Safety of Boostrix Polio Vaccine as a Booster Dose in 5 to 6-year-old Children.
NCT00871000
GlaxoSmithKlinePhase 3
TerminatedFeasibility Study of GlaxoSmithKline Biologicals' GSK2202083A Vaccine in Healthy Infants at 3, 5 and 11 Months
NCT00871741
GlaxoSmithKlinePhase 2
CompletedImmunogenicity and Safety of Kinrix + (Measles Mumps Rubella) MMR Vaccine With and Without Varicella Vaccine i
NCT00871117
GlaxoSmithKlinePhase 3
CompletedEvaluation of GlaxoSmithKline Biologicals' Boostrix® Vaccine in Comparison With Decavac™ Vaccine.
NCT00835237
GlaxoSmithKlinePhase 3
CompletedImmunogenicity and Safety of GSK Biologicals' Infanrix Hexa in Infants
NCT00753649
GlaxoSmithKlinePhase 4
CompletedImmunogenicity and Safety of GSK Biologicals' Infanrix/Hib in Children
NCT00696423
GlaxoSmithKlinePhase 3
CompletedStudy of a New Formulation of DTPa-HBV-IPV/Hib Vaccine Administered as a Booster Dose to 18-23 Months Old Chil
NCT00611559
GlaxoSmithKlinePhase 4
CompletedSafety and Immunogenicity of a Booster Dose of GSK Biological's Boostrix-Polio Vaccine
NCT00635128
GlaxoSmithKlinePhase 4
CompletedImmunogenicity and Reactogenicity of a Booster Dose of GSK Bio's DTPa-HBV-IPV/Hib Vaccine
NCT00627458
GlaxoSmithKlinePhase 2
CompletedImmunogenicity & Reactogenicity of Boostrix 10 Years After Previous Booster Vaccination.
NCT00610168
GlaxoSmithKlinePhase 4
CompletedImmunogenicity & Reactogenicity of Boostrix 10 Years After Previous Booster Vaccination in Study NCT01267058
NCT00548171
GlaxoSmithKlinePhase 4
CompletedPersistence Study of GSK Biologicals' Tdap Vaccine 1, 3, 5 and 9 Years Following Administration as an Initial
NCT00489970
GlaxoSmithKlinePhase 3
CompletedPneumococcal Vaccine Booster Study in Healthy Children 11-18 Months Old Previously Primed With the Same Vaccin
NCT00463437
GlaxoSmithKlinePhase 3
CompletedStudy to Assess Safety & Immunogenicity of GSK Biologicals' Boostrix (dTpa) Vaccine vs. Chinese DT Vaccine
NCT00452686
GlaxoSmithKlinePhase 3
CompletedStudy to Assess Safety & Immunogenicity of GSK Biologicals' DTPa/Hib Vaccine vs Separate Administration of DTP
NCT00412854
GlaxoSmithKlinePhase 3
CompletedStudy to Assess the Safety & Reactogenicity of GSK Biologicals' dTpa Vaccine (Boostrix) When Given at 6-8 Year
NCT00406562
GlaxoSmithKlinePhase 3
CompletedImmunogenicity, Safety of GSKs Tdap Vaccine Boostrix When Coadministered With GSKs Influenza Vaccine Fluarix i
NCT00385255
GlaxoSmithKlinePhase 3
CompletedImmunogenicity and Safety of a DTPa-HBV-IPV/Hib Vaccine Given at 2, 3 and 4 Months of Age
NCT00376779
GlaxoSmithKlinePhase 2
CompletedStudy to Assess the Safety & Reactogenicity of GSK Biologicals' DTPa/Hib Vaccine When Given at 3, 4 and 5 Mont
NCT00379977
GlaxoSmithKlinePhase 3
CompletedSafety and Immunogenicity of GSK's Tdap Vaccine (Boostrix) in Adults Aged 19 to 64 Years
NCT00346073
GlaxoSmithKlinePhase 3
CompletedCompare Immunogenicity & Safety of 2 Formulations of GSK Biologicals' DTPa-HBV-IPV/Hib Vaccine Given in Health
NCT00320463
GlaxoSmithKlinePhase 3
CompletedPost-marketing Safety Study of GSK Biologicals' Boostrix® Vaccine
NCT00297856
GlaxoSmithKline
CompletedUS-licensed Combined Vaccine Against Tetanus & Diphtheria, Given With US-licensed Vaccine Against Meningococca
NCT00282295
GlaxoSmithKlinePhase 4
CompletedEvaluation of the Immunogenicity, Safety and Reactogenicity of the Combined DTPa-IPV Vaccine in Healthy Infant
NCT00290342
GlaxoSmithKlinePhase 3
CompletedImmunogenicity & Safety of GSK's Combined DTPa-HBV-IPV/Hib Vaccine in Indian Infants at 2 Diff Vaccination Sch
NCT00316147
GlaxoSmithKlinePhase 3
CompletedMulticentre Booster & Immune Memory Study of a Booster Dose of GSK Biologicals' 10-valent Pneumococcal Conjuga
NCT00307567
GlaxoSmithKlinePhase 2
CompletedImmune Response and Safety Comparison of 3 Lots of GSK Biologicals' DTaP-IPV Candidate Vaccine to DTaP + IPV V
NCT00148941
GlaxoSmithKlinePhase 3
CompletedAssess the Safety & Reactogenicity of DTPa-IPV/Hib Vaccine Administered at 3, 4, 5 & 18 Mths of Age, in Health
NCT00325156
GlaxoSmithKlinePhase 4
CompletedSafety of DTPa-IPV/Hib & DTPa-HBV-IPV/Hib, Followed by DTPa-IPV/Hib Vaccine in Infants Who Received Hepatitis
NCT00325143
GlaxoSmithKlinePhase 3
CompletedAssessment of GSK Biologicals' Tdap Candidate Vaccine Administered as a Booster (6th Dose) in Terms of Immunog
NCT00263679
GlaxoSmithKlinePhase 3
CompletedComparison of Immunogenicity and Reactogenicity of INFANRIX™ HEXA and HEXAVAC™ Vaccines as a Primary Vaccinati
NCT01457547
GlaxoSmithKlinePhase 4
CompletedImmunogenicity & Safety Study of Combined/Separate Vaccine(s) Against Common Diseases in Infants (2,4,6 Months
NCT00352963
GlaxoSmithKlinePhase 3
CompletedPost Market Surveillance for Infanrix™
NCT00908115
GlaxoSmithKline
TerminatedImmunogenicity, Antibody Persistence and Safety of GSK Biologicals' DTPa (INFANRIX) and dTpa (BOOSTRIX) Vaccin
NCT00544271
GlaxoSmithKlinePhase 4
CompletedImmunogenicity and Reactogenicity Study of BoostrixTM (dTpa) and Boostrix-IPV (dTpa-IPV)
NCT01294605
GlaxoSmithKlinePhase 4
CompletedPost-marketing Safety Study of GSK Biological's Pediarix™ Vaccine
NCT00146835
GlaxoSmithKline
CompletedComparison of GSK Biologicals' DTaP-IPV Candidate Vaccine to DTaP and IPV Separately Administered Vaccines in
NCT00263692
GlaxoSmithKlinePhase 2
CompletedA Combined Tdap Vaccine Used As A Booster Compared To Licensed Td Vaccine
NCT00109330
GlaxoSmithKlinePhase 3
CompletedComparison of GSK Biologicals' Reduced Antigen Diphtheria and Tetanus Toxoids and Acellular Pertussis- Inactiv
NCT01277705
GlaxoSmithKlinePhase 3
CompletedImmunogenicity and Reactogenicity of GSK Bio DTPa-HBV-IPV and Hib Vaccines When Coadministered to Healthy Infa
NCT00879827
GlaxoSmithKlinePhase 3
CompletedImmunogenicity and Reactogenicity of DTPa-HBV-IPV/Hib Vaccine Followed by the Same Vaccine and Oral Polio Vacc
NCT01457560
GlaxoSmithKlinePhase 3