A Phase 3b Study to Assess the Safety of Novartis Meningococcal B Recombinant Vaccine When Administered in Healthy At-risk Adults
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|ClinicalTrials.gov Identifier: NCT01478347|
Recruitment Status : Completed
First Posted : November 23, 2011
Results First Posted : March 6, 2015
Last Update Posted : March 27, 2015
The proposed study will evaluate the safety of the rMenB+OMV NZ in an adult population potentially at risk for meningococcal disease (e.g. lab workers).
In the second part of the study additional blood samples of high responding vaccinated subjects will be collected for the purpose of generating a control serum panel for the human serum bactericidal assay (hSBA) tests.
|Condition or disease||Intervention/treatment||Phase|
|Meningococcal Disease Meningococcal Meningitis||Biological: Recombinant meningococcal B + OMV NZ||Phase 3|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||18 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||A Phase 3b, Single-Center, Open-label Study to Assess the Safety of Novartis Meningococcal B Recombinant Vaccine When Administered at a 0, 2-Month Schedule in Healthy At-risk Adults|
|Study Start Date :||May 2013|
|Actual Primary Completion Date :||March 2014|
|Actual Study Completion Date :||November 2014|
Experimental: rMenB+OMV NZ
Healthy adults (≥18 to ≤65 years), at high risk for meningococcal B disease due to routine occupational exposure to N. Meningitidis cultures (e.g. lab workers), were administered two injections of Recombinant meningococcal B (rMenB) + Outer Membrane Vesicle (OMV NZ) vaccine, 2 months apart, in part I of the study, were enrolled for optional blood draws and safety follow-up in part II of the study.
Biological: Recombinant meningococcal B + OMV NZ
2 injections 2 months apart
- Number of Subjects Reporting Unsolicited Adverse Events, Following Vaccination With Two Injections of rMenB+OMV NZ Vaccine Between Day 1 Through Day 91. [ Time Frame: Day 1 to day 91 ]The number of subjects with serious adverse events (SAE), medically attended adverse events and adverse events (AEs) leading to premature withdrawal, following two injections of rMenB+OMV NZ vaccine are reported.
- Number of Subjects (Who Had Received Two Injections of rMenB+OMV NZ Vaccine in Part I of This Study) Reporting Unsolicited Adverse Events During Safety Follow-up (Part II of the Study). [ Time Frame: Day 92 to day 331 ]The number of subjects (who had received two injections of rMenB + OMV NZ vaccine in the part I of this study) reporting unsolicited AEs during the safety follow-up in part II of the study, are reported. Unsolicited AEs in part two of the study include - AEs considered to be related to blood draw procedure and all SAEs.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01478347
|UOC Medicina Interna 2, Azienda Ospedaliera Universitaria Senese|
|Siena, Italy, 53100|
|Study Chair:||Novartis Vaccines||Novartis Vaccines|