Assessment of Antibody Persistence at Eighteen Months After the Completion of the Vaccination Course in Study V72P10

NCT01148524 | Completed Phase 2 Results

• 1 other identifier: V72P10E1
• Study Type: interventional
• Target: 817
• Locations: 1 country
• Sites: 6

Brief Summary

This was a Phase 2b/3, multi-center, extension study of V72P10 to assess antibody persistence at 18 months after the vaccination course in study V72P10 (NCT00661713). Subjects who participated in study V72P10, and who meet all other enrollment criteria for this extension study, and a group of naïve subjects (defined as subjects who had never received rMenB+OMV NZ or other experimental MenB vaccines) of similar age to the subjects who were eligible to participate in this extension study, performed one study visit in which a single blood sample was drawn for MenB serological analyses.

Conditions

Meningococcal Disease; Meningococcal Meningitis

Keywords

Meningococcal disease; Vaccines; Adolescents

Outcome Measures

Primary Outcomes (4)

• Percentage of Subjects With hSBA Titers ≥1:4 Against Meningococcal Strains, At 18 Months After Month-6 Vaccination in V72P10 Study, and in Naive Subjects.

  The immune response was measured as the percentage of subjects with hSBA titers ≥1:4 against meningococcal strains 44/76-SL, 5/99 and NZ98/254, at 18 months after month-6 vaccination of rMenB+OMV-NZ or placebo in V72P10 study, and in age-matched vaccine naive subjects enrolled in this study, evaluated by serum bactericidal assay using human complement (hSBA).

  month 0 (bl=baseline), month 1 and 18 months after last vaccination in V72P10 study.

• Geometric Mean hSBA Titers Directed Against Meningococcal Strains, At 18 Months After Month-6 Vaccination in V72P10 Study, and in Naive Subjects.

  The immune response was measured as the hSBA geometric mean titers (GMTs) directed against meningococcal strains 44/76-SL, 5/99 and NZ98/254, at 18 months after month-6 vaccination of rMenB+OMV-NZ or placebo in V72P10 study, and in age-matched vaccine naive subjects enrolled in this study.

  month 0 (bl=baseline), month 1 and 18 months after last vaccination in V72P10 study.

• Geometric Mean Ratio at 18 Months After Month-6 Vaccination, Over Baselines at Month 0 and at One Month After the Last rMenB+OMV-NZ Vaccination in the V72P10 Study.

  The immune response was measured as the geometric mean ratio (GMRs) of hSBA GMTs against meningococcal strains 44/76-SL, 5/99 and NZ98/254 as follow: GMTs at 1 month after last vaccination to baseline GMTs; GMTs at 18 months after last vaccination to baselines GMTs; and GMTs at 18 months after last vaccination to GMTs at 1 month after last vaccination.

  month 0 (baseline), month 1 and 18 months after last vaccination in V72P10 study.

• Geometric Mean Concentration Against Meningococcal 287-953 Antigen, At 18 Months After Month-6 Vaccination in V72P10 Study, and in Naive Subjects.

  The immune response was measured as the geometric mean concentrations (GMCs) directed against meningococcal 287-953 antigen, evaluated using enzyme-linked immunosorbent assay (ELISA), at 18 months after month-6 vaccination of rMenB+OMV-NZ or placebo in V72P10 study, and in age-matched vaccine naive subjects enrolled in this study.

  18 months after last vaccination V72P10 study.

Study Arms (9)

rMenB06

OTHER

Subjects who had received 2 doses each of rMenB+OMV-NZ (at 0 and 6 months) and placebo (at 1 and 2 months) in V72P10 study had a blood draw.

Biological: rMenB+OMV-NZ

rMenB0

OTHER

Subjects who had received 1 dose of rMenB+OMV-NZ (at 0 month) and 3 doses of placebo (at 1, 2 and 6 months) in V72P10 study had a blood draw.

Biological: rMenB+OMV-NZ

rMenB016

OTHER

Subjects who had received 3 doses of rMenB+OMV-NZ (at 0, 1 and 6 months) and 1 dose of placebo (at 2 months) in V72P10 study had a blood draw.

Biological: rMenB+OMV-NZ

rMenB01

OTHER

Subjects who had received 2 doses each of rMenB+OMV-NZ (at 0 and 1 month) and placebo (at 2 and 6 months) in V72P10 study had a blood draw.

Biological: rMenB+OMV-NZ

rMenB026

OTHER

Subjects who had received 3 doses of rMenB+OMV-NZ (at 0, 2 and 6 months) and 1 dose of placebo (at 1 month) in V72P10 study had a blood draw.

Biological: rMenB+OMV-NZ

rMenB02

OTHER

Subjects who had received 2 doses each of rMenB+OMV-NZ (at 0 and 2 months) and placebo (at 1 and 6 months) in V72P10 study had a blood draw.

Biological: rMenB+OMV-NZ

rMenB012

OTHER

Subjects who had received 3 doses of rMenB+OMV-NZ (at 0, 1 and 2 months) and 1 dose of placebo (at 6 months) in V72P10 study had a blood draw.

Biological: rMenB+OMV-NZ

rMenB6

OTHER

Subjects who had received 1 dose of rMenB+OMV-NZ (at 6 months) and 3 doses of placebo (at 0, 1 and 2 months) in V72P10 study had a blood draw.

Biological: rMenB+OMV-NZ

Naive

OTHER

An additional study group of naïve subjects that served as a baseline comparator for assessing antibody persistence in the vaccine groups and had blood draw for serological analyses at the time of enrollment.

Biological: No Vaccine

Interventions

No Vaccine BIOLOGICAL

Naive

rMenB+OMV-NZ BIOLOGICAL

Subjects who had received either rMenB+OMV-NZ or placebo at study month 6 in V72P10 study had a blood sample drawn for serological analyses at 18 months later (-1/+3 months).

Also known as: Serogroup B meningococcal recombinant vaccine

rMenB0; rMenB01; rMenB012; rMenB016; rMenB02; rMenB026; rMenB06; rMenB6

Eligibility Criteria

• Age: 13 Years - 19 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Child (0-17), Adult (18-64)

You may qualify if:

• Informed consent was obtained from all the subjects before enrollment into the study after the nature of the study had been explained.
• Healthy adolescents, 13-19 years of age (the age window is defined as the first day the subject turns 13 years of age up to the day before the subject turns 20 years of age).
• For Minor subjects:
• subjects who had given their written assent and whose parent or legal guardians had given written informed consent at the time of enrollment, after the nature of the study had been explained.
• For Adult subjects:
• subjects who had given their written informed consent at the time of enrollment, after the nature of the study had been explained.
• Were available for the visit scheduled in the study.
• Were in good health as determined by medical history, physical examination, clinical judgment of the investigator.
• For Minor subjects: (≤18 years of age)
• subjects who had given their written assent and whose parent or legal guardians had given written informed consent at the time of enrollment, after the nature of the study had been explained.
• For Adult subjects: (older than 18 years of age)
• subjects who had given their written informed consent at the time of enrollment, after the nature of the study had been explained.
• Who had participated in the V72P10 study and had received their last vaccination 18 months (-30 + 90 days) before enrollment in V72P10E1.
• Who had completed the vaccination course in study V72P10, according to the protocol.
• Who had provided at least the blood sample one month after the last vaccination in V72P10 (blood sample at visit 6, month 7), according to the protocol.

You may not qualify if:

• For Minor subjects:
• subjects who were unwilling or unable to give written informed assent to participate in the study, and whose parent(s)/legal guardian(s) were unwilling or unable to give written informed consent to participate in the study
• For Adult subjects:
• subjects who were unwilling or unable to give written informed consent to participate in the study.
• History of any meningococcal B vaccine administration.
• Previous ascertained or suspected disease caused by N. meningitidis.
• Household contact with and/or intimate exposure to an individual with laboratory confirmed N. meningitidis.
• Antibiotic treatment within 6 days prior to enrollment.
• Any serious chronic or progressive disease according to the judgment of the investigator (e.g., neoplasm, diabetes mellitus Type I, cardiac disease, hepatic disease, neurological disease or seizure, either associated with fever or as part of an underlying neurological disorder or syndrome, autoimmune disease, HIV infection or AIDS, or blood dyscrasias or diathesis, signs of cardiac or renal failure or severe malnutrition).
• Receipt of blood, blood products and/or plasma derivatives or any parenteral immunoglobulin preparation within 90 days prior to enrollment.
• Participation in another clinical trial within 90 days prior to enrollment or planned for during study.
• Family members and household members of study staff.
• Any condition which, in the opinion of the investigator, could have interfered with the evaluation of the study objectives.

Sponsors & Collaborators

• Novartis Vaccines: lead

Study Sites (6)

Centro de Salud Lo Barnechea

Santiago, Chile

Location

Centro para vacunas en desarrollo. Hospital de Niños Roberto del Río

Santiago, Chile

Location

Escuela de Medicina de la Universidad de Valparaíso

Santiago, Chile

Location

Hospital Luis Calvo Mackenna

Santiago, Chile

Location

Liceo Jose Victorino Lastarria

Santiago, Chile

Location

Universidad de Chile. Facultad de Medicina

Santiago, Chile

Location

MeSH Terms

Conditions

Meningococcal Infections; Meningitis, Meningococcal

Condition Hierarchy (Ancestors)

Neisseriaceae Infections; Gram-Negative Bacterial Infections; Bacterial Infections; Bacterial Infections and Mycoses; Infections; Meningitis, Bacterial; Central Nervous System Bacterial Infections; Central Nervous System Infections; Central Nervous System Diseases; Nervous System Diseases; Meningitis; Neuroinflammatory Diseases

Results Point of Contact

• Title: Posting Director
• Organization: Novartis Vaccines and Diagnostics

RegistryContactVaccinesUS@novartis.com

Study Officials

• Novartis Vaccines

  Novartis Vaccines

  STUDY CHAIR

Publication Agreements

• PI is Sponsor Employee: No
• Restriction Type: GT60
• Restrictive Agreement: Yes

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: PREVENTION
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: June 4, 2010
• First Posted: June 22, 2010
• Study Start: August 1, 2010
• Primary Completion: January 1, 2012
• Study Completion: January 1, 2012
• Last Updated: June 15, 2018
• Results First Posted: March 11, 2014

Record last verified: 2018-05

Locations

CL (6)