CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 98 enrolled
Drug / intervention
4CMenB (Bexsero®) vaccinebiological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04295733
NCT04295733N/ACompleted

Evaluation of Safety, Tolerability and Immunogenicity of Two Doses of the 4CMenB Vaccine in Adults With an Immunodeficiency

Ospedale Policlinico San Martino·observational·Posted Mar 4, 2020·Updated Jan 22, 2024

In Brief

An observational study evaluating 4CMenB (Bexsero®) vaccine for Acquired Immunodeficiency. Completed, enrolled 98 participants across 1 site.

Detailed Summary

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.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesItaly
CollaboratorsGlaxoSmithKline

Timeline

N/ACompletedFinished
2020202120222023202420252026
First PostedMar 4, 2020
Enrollment StartFeb 6, 2020
Primary CompletionJan 11, 2024
TodayJul 2, 2026
Enrollment to primary: 3.9 yearsPosted 6.3 years ago

Interventions

4CMenB (Bexsero®) vaccinebiological

Participants will receive 2 doses of 4CMenB (Bexsero®) vaccine administered intramuscularly 1-2 months apart