Investigating the Immunogenicity of a U.S.-Licensed Meningococcal Serogroup B Vaccine (Trumenba)

Phase

Condition

Meningitis

Treatment

N/A

Clinical Study ID

NCT02569632

ChildrensHRCOakland

Ages 18-65
All Genders
Accepts Healthy Volunteers

Study Summary

This study will investigate the breadth of protection against meningococcal disease in humans immunized with a newly FDA approved meningococcal B vaccine, trade name "Trumenba®" manufactured by Pfizer Vaccines. As a secondary goal the investigators will investigate underlying mechanisms by which human anti-FHbp antibodies elicit complement-mediated bactericidal activity.

Eligibility Criteria

Inclusion

Inclusion Criteria:

Adults in the following risk groups: physicians, nurses, respiratory therapists,microbiology laboratory personnel working at UCSF Benioff Children's Hospital Oaklandor the University of Massachusetts Medical School as well as medical studentsattending accredited U.S. medical schools
Able to comprehend and follow all required study procedures
In good health as determined by a brief medical history
For females of child bearing age a negative urine pregnancy test will be required

Exclusion

Exclusion Criteria:

Are not in the risk groups summarized above
Have not given or are unable to give written informed consent to participate in thestudy
Females of child bearing potential who are pregnant, or planning on becoming pregnantduring the study period.
Persons with a past history of having Guillain-Barré Syndrome (GBS), or a familyhistory of GBS in a parent or sibling.
Persons with presence or suspected presence of serious chronic disease including butnot limited to: chronic cardiac disease, autoimmune disease, diabetes, hepatitis B/C,HIV, progressive neurological disease or seizure, leukemia, lymphomas, or neoplasm.
Have participated in any other investigational drug or received any other vaccinewithin the last 30 days.
Received a dose of a meningococcal serogroups A, C, Y, W conjugate vaccine within theprevious 30 days or wish to receive a dose of this vaccine during the six month studyperiod.
Have a history of anaphylactic shock, asthma, urticaria or other allergic reactionafter previous dose of Trumenba
Have experienced fever (oral temperature above 38.0°C) within the past 3 days or aresuffering from a present acute infectious disease
Are planning to leave the area of the study site before the end of the study period
Have obesity (BMI higher than 33); or 11.
With any condition which, in the opinion of the investigator, might interfere with theevaluation of the study objectives.

Study Design

January 01, 2015

December 31, 2016

Study Description

Neisseria meningitidis causes meningitis and severe infections of the blood stream. The incidence of serogroup B meningococcal disease however is too low to conduct a randomized, controlled trial to determine the actual efficacy of the new serogroup B vaccines. Instead vaccine efficacy was inferred from serum bactericidal antibody responses using four test strains. However, because of strain variability of FHbp amino acid sequence (there are more than 800 sequence variants described) and strain variability of FHbp expression, bactericidal data on only four strains are unlikely to be sufficient to predict the actual strain coverage by the vaccine. There also are gaps in knowledge about the underlying mechanisms by which human antibodies to FHbp elicit complement mediated bactericidal activity. For example, binding of FH to FHbp is specific for human FH. Therefore in vaccinated humans the vaccine antigen is expected to form a complex with FH right after immunization. The investigators' hypothesis is that binding of human FH to the vaccine antigen skews the antibody repertoire to FHbp epitopes located outside of the FH combining site. The resulting antibodies would be expected not to inhibit binding of FH to the bacteria. This hypothesis will be investigated in Trumenba-immunized humans as part of studies in Aim 1 (and in future studies of recombinant human anti-FHbp Fabs that will be enabled by obtaining DNA from individual B cells, described in Aim 2).

Connect with a study center

UCSF Benioff Children's Hospital Oakland
Oakland, California 94609
United States
Site Not Available
University of Massachusetts Medical School
Worcester, Massachusetts 01655
United States
Site Not Available

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