Safety and Immunogenicity Study to Evaluate Single- or Two-Dose Regimens Of RSV F Vaccine With and Without Aluminum Phosphate or Matrix-M1™ Adjuvants In Clinically-Stable Older Adults

Novavax5 sites in 1 country300 target enrollmentJanuary 2017

ConditionsRespiratory Syncytial Viruses

Overview

Phase: Phase 2
Intervention: Not specified
Conditions: Respiratory Syncytial Viruses
Sponsor: Novavax
Enrollment: 300
Locations: 5
Primary Endpoint: Neutralizing antibody titers to at least one RSV/A strain
Status: Completed
Last Updated: 4 years ago

Overview Investigators Eligibility Criteria Outcomes Sites Similar Trials

Overview

Brief Summary

This is a randomized, observer-blind, trial in clinically-stable older adults. Up to 300 eligible older adults 60 through 80 years of age will be enrolled at a 1:1 ratio into multiple dose/formulation treatment arms. Safety and immunogenicity data through Day 56 will be used to select a vaccine candidate to potentially evaluate in a Part 2 study. Proportions of subjects in various strata will not be pre-specified and the goal will be to achieve an approximately equal distribution of subjects with these characteristics across the treatment groups. Serology measures consistent with the study outcomes will be reported.

Registry

clinicaltrials.gov

Start Date

January 2017

End Date

May 18, 2018

Last Updated

4 years ago

Study Type

Interventional

Study Design

Parallel

Sex

All

Investigators

Sponsor

Novavax

Responsible Party

Sponsor

Eligibility Criteria

Inclusion Criteria

•Males and females 60 through 80 years of age who are ambulatory and live in the community or in an assisted-living facility that provides minimal assistance, such that the subject is primarily responsible for self-care and activities of daily living. Subjects may have one or more chronic medical diagnoses, but should be clinically stable as assessed by:
•Absence of changes in medical therapy within one month due to treatment failure or toxicity (dose adjustments of ongoing therapies for optimal effect, or replacements within a class of drugs due to convenience or cost, will be deemed acceptable),
•Absence of medical events qualifying as SAEs within one month of the planned vaccination on Day 0, and
•Absence of known, current, and life-limiting diagnoses which, in the opinion of the investigator, render survival to completion of the protocol unlikely.
•Willing and able (on both a physical and cognitive basis) to give informed consent prior to study enrollment. To complete the consent process, all qualifying subjects will correctly answer at least 4 out of 5 questions of the informed consent form (ICF) comprehension assessment in no more than 2 attempts.
•Able to comply with study requirements. As the protocol procedures involve telephone contacts for safety ascertainment, eligible subjects must have a reliable access to a telephone.

Exclusion Criteria

•Received any prior RSV vaccine.
•Participation in research involving any additional investigational product (drug / biologic / device) within 45 days before planned date of first vaccination.
•History of a serious reaction to any prior vaccination or a history of Guillain-Barré syndrome (GBS) within 6 weeks of any prior influenza immunization.
•Receipt of inactivated influenza vaccine within 14 days prior to the Day 0 dose of test article or any other vaccine within the 4 weeks prior to the Day 0 dose of test article.
•Any known or suspected immunosuppressive condition, acquired or congenital, as determined by history and/or physical examination.
•Chronic administration (defined as more than 14 continuous days) of immunosuppressants or other immune-modifying drugs within 6 months prior to the administration of the study vaccine. An immunosuppressant dose of glucocorticoid will be defined as a systemic dose ≥ 10 mg of prednisone per day or equivalent. The use of topical, inhaled, and nasal glucocorticoids will be permitted.
•Administration of immunoglobulins and/or any blood products within the 3 months preceding the administration of the study vaccine or during the study.
•Acute disease at the time of enrollment (defined as the presence of a moderate or severe illness with or without fever, or an oral temperature ≥ 38.0°C on the planned day of vaccine administration).
•Known disturbance of coagulation. Potential subjects receiving aspirin, clopidogrel, prasugrel, dipyridamole, dabigatran, apixaban, rivaroxaban, or warfarin under good control for cardiovascular prophylaxis or prophylaxis of thromboembolic disease or stroke in the setting of atrial fibrillation will NOT be excluded.
•Suspicion or recent history (within one year of planned vaccination) of alcohol or other substance abuse.

Outcomes

Primary Outcomes

Neutralizing antibody titers to at least one RSV/A strain

Time Frame: Day 0, 21, 28

Subjects with solicited local and systemic AEs occurring within the 7-day period following dosings on Day 0 and Day 21 and all adverse events, solicited and unsolicited, occurring within the 56-day period of Day 0.

Time Frame: Day 0 - Day 6, Day 21 - Day 27; Day 0 - Day 56

Secondary Outcomes

Serum concentrations of antibodies competitive with palivizumab (i.e., PCA) for binding to the RSV F protein.(Day 0, 21, 28, 56, 119, 385)
Serum IgG antibody concentrations as ELISA units (EUs) specific for the F protein antigen.(Day 0, 21, 28, 56, 119, 385)
Counts of IFN-γ spot forming units following in vitro stimulation of Day 0, Day 7, and Day 28 PBMC isolates with RSV F peptides.(Day 0, 7, 28)
Counts and proportions of Day 0, Day 7, and Day 28 peripheral blood T cells positive by intracellular staining for IL-2, IFN-γ, or TNF-α production (alone or any combination thereof) following in vitro stimulation with RSV F peptides.(Day 0, 7, 28)