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A Clinical Trial to Study the Safety, Tolerance and Immunogenic Response to MCV4, Tdap and Bivalent rLP2086 Vaccine When Given at the Same Time to Children Between the Ages of 10 Through 12 Years of Age

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Pfizer
ClinicalTrials.gov Identifier:
NCT01461980
First received: September 28, 2011
Last updated: June 23, 2014
Last verified: June 2014

September 28, 2011
June 23, 2014
September 2011
May 2014   (final data collection date for primary outcome measure)
  • The geometric mean titers (GMTs) or geometric mean concentrations (GMCs) for each of the antibodies reactive with each of the 10 antigenic components in the marketed vaccines at visit 2, among subjects in Groups 1 and 2. [ Time Frame: Month 1 ] [ Designated as safety issue: No ]
  • The hSBA geometric mean titers (GMTs) for each of the 2 primary strains (PMB80 [A22] and PMB2948 [B24]) at visit 6, among subjects in Groups 1 and 3. [ Time Frame: Month 7 ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT01461980 on ClinicalTrials.gov Archive Site
  • The seroresponse rate at visit 2 for each of the 10 marketed vaccine antigens in Group 1 and Group 2. [ Time Frame: Month 1 ] [ Designated as safety issue: No ]
  • Proportion of subjects (Groups 1 and 2) who achieve an antibody level >=1.0 IU/mL to tetanus and proportion of subjects (Groups 1 and 2) who achieve an antibody level >1.0 IU/mL to diphtheria toxoid. [ Time Frame: Month 1 ] [ Designated as safety issue: No ]
  • hSBA titers as measured by GMTs for each of the 2 primary MnB test strains (PMB80 [A22] and PMB2948 [B24]) at each applicable blood sampling time point. [ Time Frame: Month 0, 1, 3, 7 ] [ Designated as safety issue: No ]
  • Proportion of subjects with hSBA titers ≥LLOQ, ≥1:4, ≥1:8, ≥1:16 , ≥1:32, ≥1:64, ≥1:128 at each blood draw visit, for each of the 2 primary strains (PMB80 [A22] and PMB2948 [B24]). [ Time Frame: Month 0, 1, 3, 7 ] [ Designated as safety issue: No ]
  • Exploratory immunogenicity endpoints will be applied to MCV4 antigenic components in subjects from Group 1 and Group 2. The exploratory endpoints are IgG response (measured as GMCs) in serogroups A, C, Y and W-135. [ Time Frame: Month 1 ] [ Designated as safety issue: No ]
  • Proportion of subjects achieving at least a 4-fold increase in hSBA titer from baseline to 1-month after the second and the third vaccination with the bivalent rLP2086 vaccine for each of the 2 primary strains (PMB80 [A22], PMB2948 [B24]). [ Time Frame: Month 3, 7 ] [ Designated as safety issue: No ]
  • Safety measured by subjects reporting adverse events and use of antipyretic medication. [ Time Frame: Throughout the study. ] [ Designated as safety issue: Yes ]
  • Immunogenicity measured by the proportion of subjects achieving hSBA titers greater than or equal to 1:4, 1 month after the second and third vaccination of rLP2086 for each of the 2 primary strains in Group 1 and Group 3. [ Time Frame: Months 3 and 7 ] [ Designated as safety issue: No ]
  • Immunogenicity measured by the seroresponse rate at visit 2 for each of the 10 marketed vaccine antigens in Group 1 and Group 2. [ Time Frame: Month 1 ] [ Designated as safety issue: No ]
  • Immunogenicity measured by the hSBA titers measured by GMTs for each of the 2 primary strains among subjects in Groups 1 and 3. [ Time Frame: Month 3 ] [ Designated as safety issue: No ]
  • Immunogenicity measured by the proportion of subjects (Groups 1 and 2) who achieve an antibody level greater than or equal to 1.0 IU/mL to tetanus [ Time Frame: Month 1 ] [ Designated as safety issue: No ]
  • Immunogenicity measured by the proportion of subjects (Groups 1 and 2) who achieve an antibody level greater than or equal to 1.0 IU/mL to diphtheria toxoid. [ Time Frame: Month 1 ] [ Designated as safety issue: No ]
  • Immunogenicity measured by the proportion of subjects with hSBA titers below lower limit of quantitation (LLOQ) at each applicable blood sampling time point for each of the 2 primary strains. [ Time Frame: Months 0, 3, and 7 ] [ Designated as safety issue: No ]
  • Immunogenicity measured by the proportion of subjects achieving at least 4 fold rise on hSBA titer for each of the 2 primary strains. [ Time Frame: Months 0, 3 and 7 ] [ Designated as safety issue: No ]
  • Immunogenicity measured by the hSBA titers measured by GMTs for each of the 2 primary strains at each applicable blood sampling time point. [ Time Frame: Months 0, 1, 3, and 7 ] [ Designated as safety issue: No ]
  • Immunogenicity measured by the proportion of subjects with hSBA titers greater than or equal to 1:4 at each blood draw visit, for each of the 2 primary strains. [ Time Frame: Months 0, 1, 3 and 7 ] [ Designated as safety issue: No ]
  • Immunogenicity measured by the proportion of subjects with hSBA titers greater than or equal to 1:8 at each blood draw visit, for each of the 2 primary strains. [ Time Frame: Months 0, 1, 3 and 7 ] [ Designated as safety issue: No ]
  • Immunogenicity measured by the proportion of subjects with hSBA titers greater than or equal to 1:16, at each blood draw visit, for each of the 2 primary strains. [ Time Frame: Months 1, 3, & 7 ] [ Designated as safety issue: No ]
  • Immunogenicity measured by the proportion of subjects with hSBA titers greater than or equal to 1:32, at each blood draw visit, for each of the 2 primary strains. [ Time Frame: Months 0 to 7 ] [ Designated as safety issue: No ]
  • Immunogenicity measured by the proportion of subjects with hSBA titers greater than or equal to 1:64, at each blood draw visit, for each of the 2 primary strains. [ Time Frame: Months 0 to 3 ] [ Designated as safety issue: No ]
  • Immunogenicity measured by the proportion of subjects with hSBA titers 1 greater than or equal to 1:28, at each blood draw visit, for each of the 2 primary strains. [ Time Frame: Months 0 to 3 ] [ Designated as safety issue: No ]
  • Immunogenicity measured by the geometric mean fold rise (GMFR) from Visit 1 to Visit 6 (postvaccination 3 relative to baseline) on hSBA titer for each of the 2 primary strains. [ Time Frame: Months 0,2,and 6 ] [ Designated as safety issue: No ]
  • Immunogenicity measured by the geometric mean fold rise (GMFR) from Visit 1 to Visit 4 (postvaccination 2 relative to baseline) on hSBA titer for each of the 2 primary strains. [ Time Frame: Months 0,1,and 3 ] [ Designated as safety issue: No ]
  • Safety measured by subjects reporting adverse events. [ Time Frame: Months 0 to 12 ] [ Designated as safety issue: Yes ]
Not Provided
Not Provided
 
A Clinical Trial to Study the Safety, Tolerance and Immunogenic Response to MCV4, Tdap and Bivalent rLP2086 Vaccine When Given at the Same Time to Children Between the Ages of 10 Through 12 Years of Age
A Phase 2, Randomized, Active-Controlled, Observer-Blinded Trial to Assess the Safety, Tolerability and Immunogenicity of MCV4, Tdap Vaccine and Bivalent rLP2086 Vaccine When Administered Concomitantly in Healthy Subjects Aged > = to 10 Years to Less Than 13 Years

This is a clinical study to assess the safety, tolerance and immunogenic response to MCV4(quadrivalent meningococcal polysaccharide conjugate, meningococcal serogroups A,C,Y, and W135), Tdap (diphtheria, tetanus, and acellular pertussis), and bivalent rLP2086 vaccine. Healthy male and female subjects, between the ages of 10 to 12 years old, will be randomized into 1 of 3 groups. The subjects, investigators, site staff and sponsor will be blinded to all injections given throughout the study. An unblinded administrator will be responsible to administer the vaccinations to all subjects and will be unblinded to the subject randomization in order to determine which subjects were in randomized to group 3 so they may receive their catch-up vaccinations of MCV4 and Tdap. A final telephone contact will be conducted with all subjects 6-months post their last vaccination to obtain safety information.

Not Provided
Interventional
Phase 2
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Primary Purpose: Prevention
  • Vaccines
  • Meningococcal Vaccines
  • Biological: rLP2086 + MCV4 + Tdap
    At visit 1, group 1 will receive MCV4 + Tdap vaccines concomitantly with an injection of rLP2086. At visits 3 and 5 (Months 2 and 6), group 1 will receive an injection of rLP2086.
  • Biological: MCV4 + Tdap + saline
    At visit 1, group 2 will receive MCV4 + Tdap vaccines concomitantly with an injection of saline. At visits 3 and 5 (months 2 and 6), this group will receive a saline injection only.
  • Biological: rLP2086 + saline
    At visit 1, group 3 will receive 2 injections of saline concomitantly with an injection of rLP2086. At visits 3 and 5 (Months 2 and 6), group 3 will receive an injection of rLP2086. Subjects randomized to this group will receive MCV4 and Tdap following their final visit blood draw (Visit 6).
  • Active Comparator: MCV4 + Tdap+ rLP2086
    Group 1 - MCV4 + Tdap + rLP2086
    Intervention: Biological: rLP2086 + MCV4 + Tdap
  • Active Comparator: MCV4 + Tdap + saline
    Group 2, MCV4 + Tdap+ saline
    Intervention: Biological: MCV4 + Tdap + saline
  • Placebo Comparator: Saline + saline + rLP2086
    Group 3- rLP2086 + saline
    Intervention: Biological: rLP2086 + saline
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
2657
May 2014
May 2014   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Evidence of a personally signed and dated informed consent document (ICD) indicating that the subject (and a legally authorized representative) has been informed of all pertinent aspects of the study.
  • Parent /legally authorized representative and subjects who are willing and able to comply with scheduled visits, laboratory tests, and other study procedures.
  • Male or female subject aged greater than or equal to 10 and <13 years at the time of enrollment.
  • Available for the entire study period and can be reached by telephone.
  • Healthy subject as determined by medical history, physical examination, and judgment of the investigator.
  • Has received full series (5-dose series is preferred, 4-dose catch up series is allowed) of diphtheria, tetanus and pertussis (whole cell or acellular) vaccines per country specific recommendations applicable at the time of receipt.
  • Male and female subjects of childbearing potential must agree to use a highly effective method of contraception throughout the study.

Exclusion Criteria:

  • Previous vaccination with any meningococcal serogroup B vaccine.
  • Vaccination with any diphtheria, tetanus or pertussis vaccine within 5 years of the first study vaccination.
  • Previous vaccination with any MCV4 vaccine.
  • A previous anaphylactic reaction to any vaccine or vaccine-related component.
  • Contraindication to vaccination with MCV4 and/or Tdap vaccine.
  • Subjects receiving any allergen immunotherapy with a non-licensed product or receiving allergen immunotherapy with a licensed product and are not on stable maintenance doses.
  • Bleeding diathesis or condition associated with prolonged bleeding time that would contraindicate intramuscular injection.
  • A known or suspected defect of the immune system that would prevent an immune response to the vaccine, such as subjects with congenital or acquired defects in B cell function, those receiving chronic systemic (oral, intravenous or intramuscular) corticosteroid therapy, or those receiving immunosuppressive therapy. Subjects with terminal complement deficiency may not be included.
  • History of culture-proven disease caused by Neisseria meningitidis or Neisseria gonorrhoea.
  • Significant neurological disorder or history of seizure (excluding simple febrile seizure).
  • Receipt of any blood products, including immunoglobulin within 6 months before the first study vaccination.
  • Current chronic use of systemic antibiotics.
  • Any neuroinflammatory or autoimmune condition, including, but not limited to, transverse myelitis, uveitis, optic neuritis, and multiple sclerosis.
Both
10 Years to 12 Years
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01461980
B1971015, 6108A1-2005
Yes
Pfizer
Pfizer
Not Provided
Study Director: Pfizer CT.gov Call Center Pfizer
Pfizer
June 2014

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP