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A Phase 3b Study to Assess the Safety of Novartis Meningococcal B Recombinant Vaccine When Administered in Healthy At-risk Adults

This study is ongoing, but not recruiting participants.
Sponsor:
Information provided by (Responsible Party):
Novartis ( Novartis Vaccines )
ClinicalTrials.gov Identifier:
NCT01478347
First received: November 21, 2011
Last updated: July 10, 2014
Last verified: July 2014

November 21, 2011
July 10, 2014
May 2013
March 2014   (final data collection date for primary outcome measure)
Number of subjects exposed to study vaccines with reported serious adverse events (SAEs) and/or adverse events (AEs) [ Time Frame: from day 1 to day 90 ] [ Designated as safety issue: Yes ]
To descriptively assess the safety of Novartis rMenB+OMV NZ in healthy at-risk adults when administered at a 0,2- month schedule, throughout the clinical study.
All SAEs, AEs that result in a subject's withdrawal from the study and medically attended AEs will be collected throughout the study period (i.e., from ICF signature up to Visit 3, 1 month after last vaccination. [ Time Frame: 3 months ] [ Designated as safety issue: Yes ]
Complete list of historical versions of study NCT01478347 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
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A Phase 3b Study to Assess the Safety of Novartis Meningococcal B Recombinant Vaccine When Administered in Healthy At-risk Adults
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

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 portion 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.

Not Provided
Interventional
Phase 3
Allocation: Non-Randomized
Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Prevention
  • Meningococcal Disease
  • Meningococcal Meningitis
Biological: Recombinant meningococcal B + OMV NZ
2 dose 2 months apart
Experimental: Arm 1
rMenB+OMV NZ
Intervention: Biological: Recombinant meningococcal B + OMV NZ
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
18
January 2015
March 2014   (final data collection date for primary outcome measure)

Inclusion criteria:

  1. 18 - 65 years of age inclusive who have given written informed consent at the time of enrollment;
  2. Able to comprehend and follow all required study procedures;
  3. Who are available for all the visits scheduled in the study (i.e., not planning to leave the area before the end of the study period);
  4. In good health as determined by the outcome of medical history, physical examination and clinical judgment of the investigator;
  5. Who were or might be routinely exposed to N. meningitidis cultures

Inclusion criteria for protocol part 2

  1. 18 - 65 years of age inclusive;
  2. At least 50 kg weight;
  3. Blood pressure within the following ranges: Systolic 110-180; Diastolic 60-100;
  4. Regular pulse rate (50-90 beats per minute) - exceptions are acceptable upon investigator's judgment;
  5. Hematocrit higher than: 32% for women and 35% for males;
  6. Visit 3 sera suitable as control for standardization of the SBA as confirmed by the central laboratory.

Exclusion criteria:

  1. History of any serogroup B meningococcal vaccine administration
  2. History of severe allergic reactions after previous vaccinations or hypersensitivity to any vaccine component;
  3. Pregnancy or nursing (breastfeeding) mothers;
  4. Females of childbearing age who have not used or do not plan to use acceptable birth control measures, for the duration of the study. Oral, injected or implanted hormonal contraceptive, barrier methods (condom or diaphragm with spermicide), intrauterine device, surgical sterilization, transdermal delivery, congenital sterility or sexual abstinence are considered acceptable forms of birth control. If sexually active the subject must have been using one of the accepted birth control methods at least one months prior to study entry;
  5. Known or suspected autoimmune disease or impairment/alteration of the immune system resulting from (for example):

    • Receipt of any chronic immunosuppressive therapy
    • Receipt of any chronic immunostimulants
    • Immune deficiency disorder, or known HIV infection
  6. Known bleeding diathesis or any condition that may be associated with a prolonged bleeding time.
  7. History or any illness/condition which, in the opinion of the investigator, might interfere with the evaluation of the study objectives or pose additional risk to the subjects due to participation in the study.
  8. Any significant chronic infection.
  9. Any serious chronic or progressive disease according to judgment of the investigator (e.g. neoplasm, insulin dependent diabetes, cardiac, renal or hepatic disease).

Exclusion criteria for protocol part 2:

  1. Known or suspected autoimmune disease;
  2. Any serious chronic or progressive disease according to judgment of the investigator (e.g. neoplasm, diabetes, cardiovascular, renal, hepatic, immunological, metabolic, urogenital, hematological, gastrointestinal, central nervous system disease);
  3. Known bleeding diathesis or any condition that may be associated with a prolonged bleeding time;
  4. History of fainting or seizure episodes;
  5. Pregnancy;
  6. Any significant chronic infection.
  7. Significant acute infections within the previous 2 weeks or body temperature >38.0C within the previous 2 weeks.
  8. Known or suspected autoimmune disease or impairment/alteration of the immune system resulting from (for example):

    • Receipt of any chronic immunosuppressive therapy
    • Receipt of any chronic immunostimulants
    • Immune deficiency disorder, or known HIV infection
  9. Significant acute illness within the previous 7 days or body temperature >38.0C within the previous 3 days.
  10. Receipt of systemic antibiotics within the previous 3 days (72 hours).
Both
18 Years to 65 Years
Yes
Contact information is only displayed when the study is recruiting subjects
Italy
 
NCT01478347
V72_37
No
Novartis ( Novartis Vaccines )
Novartis Vaccines
Not Provided
Study Chair: Novartis Vaccines Novartis Vaccines
Novartis
July 2014

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP