NCT03026348

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
300

participants targeted

Target at P75+ for phase_2

Timeline
Completed

Started Jan 2017

Shorter than P25 for phase_2

Geographic Reach
1 country

5 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2017

Completed
16 days until next milestone

First Submitted

Initial submission to the registry

January 17, 2017

Completed
3 days until next milestone

First Posted

Study publicly available on registry

January 20, 2017

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2017

Completed
1.1 years until next milestone

Study Completion

Last participant's last visit for all outcomes

May 18, 2018

Completed
Last Updated

December 6, 2021

Status Verified

December 1, 2021

Enrollment Period

3 months

First QC Date

January 17, 2017

Last Update Submit

December 2, 2021

Conditions

Keywords

RSV

Outcome Measures

Primary Outcomes (2)

  • Neutralizing antibody titers to at least one RSV/A strain

    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.

    Day 0 - Day 6, Day 21 - Day 27; Day 0 - Day 56

Secondary Outcomes (4)

  • 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

Study Arms (12)

Treatment Group A

ACTIVE COMPARATOR

Day 0 RSV F Vaccine 135µg/0.5mL Day 21 Phosphate Buffer

Biological: RSV F VaccineOther: Phosphate Buffer

Treatment Group B

ACTIVE COMPARATOR

Day 0 Treatment / Formulation 1 Day 21 Phosphate Buffer

Biological: RSV F Vaccine with Aluminum Phosphate AdjuvantOther: Phosphate Buffer

Treatment Group C

ACTIVE COMPARATOR

Day 0 Treatment / Formulation 1 Day 21 Treatment / Formulation 1

Biological: RSV F Vaccine with Aluminum Phosphate Adjuvant

Treatment Group D

ACTIVE COMPARATOR

Day 0 Treatment / Formulation 2 Day 21 Phosphate Buffer

Biological: RSV F Vaccine with Aluminum Phosphate AdjuvantOther: Phosphate Buffer

Treatment Group E

ACTIVE COMPARATOR

Day 0 Treatment / Formulation 2 Day 21 Treatment / Formulation 2

Biological: RSV F Vaccine with Aluminum Phosphate Adjuvant

Treatment Group F

ACTIVE COMPARATOR

Day 0 Treatment / Formulation 3 Day 21 Phosphate Buffer

Biological: RSV F VaccineBiological: Matrix-M1 AdjuvantOther: Phosphate Buffer

Treatment Group G

ACTIVE COMPARATOR

Day 0 Treatment / Formulation 3 Day 21 Treatment / Formulation 3

Biological: RSV F VaccineBiological: Matrix-M1 Adjuvant

Treatment Group H

ACTIVE COMPARATOR

Day 0 Treatment / Formulation 4 Day 21 Phosphate Buffer

Biological: RSV F VaccineBiological: Matrix-M1 AdjuvantOther: Phosphate Buffer

Treatment Group J

ACTIVE COMPARATOR

Day 0 Treatment / Formulation 4 Day 21 Treatment / Formulation 4

Biological: RSV F VaccineBiological: Matrix-M1 Adjuvant

Treatment Group K

ACTIVE COMPARATOR

Day 0 Treatment / Formulation 5 Day 21 Phosphate Buffer

Biological: RSV F VaccineBiological: Matrix-M1 AdjuvantOther: Phosphate Buffer

Treatment Group L

ACTIVE COMPARATOR

Day 0 Treatment / Formulation 5 Day 21 Treatment / Formulation 5

Biological: RSV F VaccineBiological: Matrix-M1 Adjuvant

Treatment Group M

PLACEBO COMPARATOR

Day 0 Phosphate Buffer Day 21 Phosphate Buffer

Other: Phosphate Buffer

Interventions

Treatment Group BTreatment Group CTreatment Group DTreatment Group E
RSV F VaccineBIOLOGICAL
Treatment Group ATreatment Group FTreatment Group GTreatment Group HTreatment Group JTreatment Group KTreatment Group L
Treatment Group FTreatment Group GTreatment Group HTreatment Group JTreatment Group KTreatment Group L
Treatment Group ATreatment Group BTreatment Group DTreatment Group FTreatment Group HTreatment Group KTreatment Group M

Eligibility Criteria

Age60 Years - 80 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.
  • Any condition that in the opinion of the investigator would pose a health risk to the subject if enrolled or could interfere with evaluation of the vaccine or interpretation of study results (including neurologic, cognitive, or psychiatric conditions deemed likely to impair the quality of study compliance or safety reporting).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (5)

Research Site AU004

Sydney, New South Wales, Australia

Location

Research Site AU005

Herston, Queensland, 4006, Australia

Location

Research Site AU002

Adelaide, South Australia, 50000, Australia

Location

Research Site AU006

Prahran, Victoria, 3181, Australia

Location

Resarch Site AU001

Nedlands, Western Australia, 6009, Australia

Location

MeSH Terms

Interventions

Matrix-M

Study Officials

  • Clinical Development

    Novavax

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
phase 2
Allocation
RANDOMIZED
Masking
QUADRUPLE
Who Masked
PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 17, 2017

First Posted

January 20, 2017

Study Start

January 1, 2017

Primary Completion

April 1, 2017

Study Completion

May 18, 2018

Last Updated

December 6, 2021

Record last verified: 2021-12

Locations