Safety, Tolerability and Immunogenicity of 4CMenB Vaccine(2 Doses) in Adults With an Immunodeficiency

Ospedale Policlinico San Martino

Status

Completed

Conditions

Acquired Immunodeficiency

Treatments

Biological: 4CMenB (Bexsero®) vaccine

Study type

Observational

Funder types

Other

Industry

Identifiers

NCT04295733

4CMenB

Details and patient eligibility

About

The meningococcal quadrivalent conjugate vaccine (MenACWY) and the licenced multicomponent MenB vaccine (Bexsero®) have already been included in the Italian childhood immunization programme and recommendations for high risk categories have been also implemented.

As by NIP, vaccination against MenB with either 4CMenB or fHbp-MenB is offered for free for several conditions including subjects with severe primary or secondary immunodeficiency.

In Liguria Region meningococcal vaccination is actively offered to several chronic conditions including asplenia, patients with lymphoproliferative disease (also HSCT), subject treated with anti-CD20 mAb and HIV-positive.

In Liguria Region there is a large diverse population with risk condition that, as by national and regional recommendation, receive meningococcal vaccination. For some of them, i.e. asplenic and complement deficiencies groups, evidence have been generated through an ad hoc clinical trial, while for other important groups there is clear need of immunogenicity data.

In the proposed study, the Investigators plan to administer two doses of MenB vaccine (Bexsero®), 1-2 months apart, to adult patients living in Genoa area and belonging to following categories:

Bone marrow transplant (HSCT patient)
HIV positive
Alfa-CD20 subjects (i.e. Patients candidates for / in treatment with biologic drugs such as Rituximab).

Immunogenicity data will be then obtained from sera collected at the day of the first Bexsero dose and one month after the immunization course by Serum Bactericidal Activity (SBA) assay.

Enrollment

98 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Males and females 18 through 65 years of age at the time of enrollment who are high risk for IMD, including subjects with documented medical history of any of the following criteria:
1. Hematopoietic Stem Celi Transplantation (allogenic or autologous stem celi transplant)
2. HIV infection
3. candidate for / in treatment (ongoing) with biological drugs such as monoclonal antibodies anti CD- 20 (rituximab or ocrelizumab)
Written informed consent obtained from the subject (or legal representative).
Subjects (or legal representative) who are able to comprehend all procedures and to comply with the study requirements

Exclusion criteria

Subjects not able to understand and to adhere to ali study procedures
Subjects aged <18 or >65 years
Known or suspected allergy/hypersensitivity to any vaccine component
History of serious adverse reaction to any vaccine
Administration of immunoglobulins and/or any blood products within 3 months prior to enrollment or planned administration during the entire study period
History of any meningococcal group B vaccination or having been diagnosed with meningococcal disease ever before
Stem celi transplantation within 6 months before the enrollment to the study
HIV-infected patients with detectable viral load (>50 copies/mL) and/or CD4 celi count < 200 cells/mm3 in the last 6 months
Receipt of any vaccine within 28 (for live vaccines) or 14 (for no-live vaccines) days prior to study vaccination
Planned vaccination (other than the study vaccination) during the entire study period
Fever or any acute disease or infection within 3 days prior to vaccination
Receipt of any antibiotics within 3 days before enrollment
Coagulation disorder contraindicating intramuscular vaccination Any condition that in the opinion of the investigator would pose a health risk to the subject if enrolled or could interfere with the study procedures
Current participation to another investigational study or planned enrollment to an investigational during the entire study period
Planned surgery or hospitalization during the entire study period
Subjects who participated in Cohort 1, 2 or 3, cannot be included in other different cohorts
Pregnancy or breastfeeding (asking the woman to sign a declaration that she is not pregnant or breastfeeding).
Any contraindication to the study vaccine (Bexsero®) as specified in the Summary of Product Characteristics.