Safety and Immunogenicity of the RSV-F Vaccine in Older Adults Previously Treated With the Same Vaccine or Placebo in the Prior Year.

NCT ID: NCT02593071

Last Updated: 2022-05-27

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 1330 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-10-31
• Study Completion Date: 2016-11-30

Brief Summary

This study will enroll subjects who received the RSV F vaccine or placebo in the earlier study (RSV-E-201, Year 1) and re-randomize them to receive either vaccine or placebo in a second season. This design will permit evaluation of the safety and immunogenicity of revaccination in a second RSV season, and the safety and immunogenicity of revaccination over two years.

Conditions

Respiratory Syncytial Virus (RSV)

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: TRIPLE

Study Groups

Treatment Group A

RSV-F Vaccine ( 0.5mL Injection)

Group Type: EXPERIMENTAL

RSV-F Vaccine

Intervention Type: BIOLOGICAL

Treatment Group B

Phosphate Buffer Placebo (0.5mL Injection)

Group Type: PLACEBO_COMPARATOR

Phosphate Buffer Placebo

Intervention Type: BIOLOGICAL

Interventions

RSV-F Vaccine

Intervention Type: BIOLOGICAL

Phosphate Buffer Placebo

Intervention Type: BIOLOGICAL

Eligibility Criteria

Inclusion Criteria

1. Males and females ≥60 years of age who are veterans of the RSV-E-201 clinical trial and who are ambulatory and live in the community or in residential facilities which provide 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,
• Absence of medical events qualifying as SAEs within two months, and
• Absence of known, current, life-limiting diagnoses that, in the opinion of the investigator, render survival to trial completion unlikely.

2. Willing and able (on both a physical and cognitive basis) to give informed consent prior to study enrollment.

3. Able to comply with study requirements, including access to transportation for study visits. The investigator may use his/her discretion to assess potential ability and willingness to comply based on performance in the prior trial, RSV-E-201.

4. Access to inbound and outbound communication by telephone with caregivers and study staff.

Exclusion Criteria

1. Participation in research involving investigational product (drug / biologic / device) within 45 days before planned date of first vaccination, with the exception of participation in the preceding study RSV-E-201.

2. History of a serious reaction to any prior vaccination, or Guillain-Barré syndrome (GBS) within 6 weeks of any prior influenza immunization, or withdrawal from the preceding RSV-E-201 clinical trial due to an adverse event deemed test article-related or at the advice of the investigator.

3. Receipt of any vaccine other than IIV in the 4 weeks preceding the study vaccination; or any RSV vaccine at any time unless administered in the preceding study, RSV-E-201.

4. Any known or suspected immunosuppressive condition, acquired or congenital, as determined by history and/or physical examination.

5. 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 ≥10mg of prednisone per day or equivalent. The use of topical, inhaled, and nasal glucocorticoids will be permitted.

6. Administration of immunoglobulins and/or any blood products within the 3 months preceding the administration of the study vaccine or during the study.

7. 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).

8. 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.

9. Suspicion or recent history (within one year of planned vaccination) of alcohol or other substance abuse.

10. 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).

• Minimum Eligible Age: 60 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Novavax

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Clinical Development

Role: STUDY_DIRECTOR

Novavax, Inc.

Locations

Nothern California Clinical Research

Redding, California, United States

Clinical Research Atlanta

Stockbridge, Georgia, United States

Johnson County Clin-Trials

Lenexa, Kansas, United States

Rapid Medical Research

Cleveland, Ohio, United States

Clinical Research Associates

Nashville, Tennessee, United States

Research Across America

Dallas, Texas, United States

Clinical Trials of Texas

San Antonio, Texas, United States

Advanced Clinical Research

West Jordan, Utah, United States

Group Health Research Institute

Seattle, Washington, United States

Marshfield Clinical Research Foundation

Wausau, Wisconsin, United States

Countries

United States

Other Identifiers

RSV-E-202

Identifier Type: -

Identifier Source: org_study_id