Safety Study of Respiratory Syncytial Virus (RSV)-Fusion (F) Protein Particle Vaccine

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Novavax
ClinicalTrials.gov Identifier:
NCT01290419
First received: February 2, 2011
Last updated: March 6, 2012
Last verified: March 2012

February 2, 2011
March 6, 2012
December 2010
December 2011   (final data collection date for primary outcome measure)
To assess and compare the safety, reactogenicity, and tolerability of 6 RSV-F protein particle vaccine formulations. [ Time Frame: Day 60 (2 months) ] [ Designated as safety issue: Yes ]

This primary outcome will be evaluated through an assessment of the following parameters:

  • Immediate AEs
  • Solicited AEs
  • All SAEs and SNMCs
  • Vital signs
  • Laboratory Assessments
To assess and compare the safety, reactogenicity, and tolerability of 4 RSV-F vaccine formulations. [ Time Frame: Day 60 (2 months) ] [ Designated as safety issue: Yes ]

This primary outcome will be evaluated through an assessment of the following parameters:

  • Immediate AEs
  • Solicited AEs
  • All nonserious AEs
  • All SAEs and SNMCs
  • Vital signs
  • Laboratory Assessments
Complete list of historical versions of study NCT01290419 on ClinicalTrials.gov Archive Site
To assess and compare the immunogenicity (neutralizing antibody and total anti-F antibody) of the 6 RSV-F protein particle vaccine formulations [ Time Frame: Day 60 (2 months) ] [ Designated as safety issue: No ]

This secondary outcome will be assessed in the following manner:

  • Neutralizing antibody against RSV measured in a PRNT assay
  • Total anti-F IgG measured by ELISA by ELISA
  • To assess and compare the immunogenicity (neutralizing and total anti-F antibody) of the 4 RSV-F vaccine formulations [ Time Frame: Day 60 (2 months) ] [ Designated as safety issue: No ]

    This secondary outcome will be assess in the following manner:

    - Antibody against RSV measured by ELISA and Micronuetralization in Hep2 cells.

  • To confirm the "dose sparing" and "value added" effects of the aluminum phosphate adjuvant [ Time Frame: Day 180 (6 months) ] [ Designated as safety issue: No ]

    This secondary outcome will be assess in the following manner:

    - cell-mediated immunity (CMI) measured in a subset of subjects.

Not Provided
Not Provided
 
Safety Study of Respiratory Syncytial Virus (RSV)-Fusion (F) Protein Particle Vaccine
A Phase 1 Randomized, Observer-Blinded,Placebo-Controlled Trial to Evaluate the Safety and Immunogenicity of a Recombinant Respiratory Syncytial Virus F Protein Particle Vaccine in Healthy Adults

A Phase 1, Randomized, Placebo-Controlled, Observer-Blinded, Escalating Dose-Ranging Study to Assess the Safety, and immunogenicity of 6 different recombinant RSV-F formulations in healthy adults (18 to 49 years of age).

Study Objectives:

Primary:

  • To assess and compare the safety, reactogenicity, and tolerability of 6 RSV-F protein particle vaccine formulations.

Secondary:

  • To assess and compare the immunogenicity (neutralizing antibody and total anti-F antibody) of the 6 RSV-F protein particle vaccine formulations
  • To confirm the "dose sparing" and "value added" effects of the aluminum phosphate adjuvant

A total of 150 subjects will be allocated to 7 cohorts. Subjects will be randomly assigned to vaccine treatment or saline placebo in a 4:1 ratio, such that each cohort will include 20 subjects who receive active vaccine (Groups A, B, C, D, F and G) and 5 subjects who receive placebo (Group E).

Subjects will be followed for all AEs, including SAEs and non-serious AEs, from the time of each vaccination through 30 days following the second vaccination (Day 60±5). After Day 60, subjects will be contacted via telephone on a monthly basis (approximately Days 90, 120, 150, 180, and 210) and asked about the occurrence of SAEs and SNMCs.

Interventional
Phase 1
Allocation: Randomized
Endpoint Classification: Safety Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Investigator)
Primary Purpose: Treatment
Respiratory Syncytial Virus Infections
  • Biological: RSV-F Particle Vaccine
    Dose 1 + adjuvant / dose; Day 0 and Day 30
  • Biological: RSV-F Particle Vaccine
    Dose 2 + adjuvant / dose; Day 0 and Day 30
  • Biological: RSV-F Particle Vaccine
    Dose 3 + adjuvant / dose; Day 0 and Day 30
  • Biological: RSV-F Particle Vaccine
    Dose 3 / dose; Day 0 and Day 30
  • Biological: Placebo
    Placebo; Day 0 and Day 30
  • Biological: RSV-F Particle Vaccine
    Dose 4 / dose; Day 0 and Day 30
  • Biological: RSV-F Particle Vaccine
    Dose 4 + adjuvant / dose; Day 0 and Day 30
  • Experimental: A: Dose 1 + adjuvant
    Intervention: Biological: RSV-F Particle Vaccine
  • Experimental: B: Dose 2 + adjuvant
    Intervention: Biological: RSV-F Particle Vaccine
  • Experimental: C: Dose 3 + adjuvant
    Intervention: Biological: RSV-F Particle Vaccine
  • Experimental: D: Dose 3 alone
    Intervention: Biological: RSV-F Particle Vaccine
  • Placebo Comparator: E: Placebo control
    Intervention: Biological: Placebo
  • Experimental: F: Dose 4 alone
    Intervention: Biological: RSV-F Particle Vaccine
  • Experimental: G: Dose 4 +adjuvant
    Intervention: Biological: RSV-F Particle Vaccine

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
150
December 2011
December 2011   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Male or female aged 18 to 49 years inclusive
  • Ability to provide written informed consent to participate
  • Healthy, as determined by medical history, physical examination, vital signs, and clinical safety laboratory examinations at baseline
  • Females are required to fulfill one of the following criteria:

    • At least 1 year post-menopausal
    • Surgically sterile
    • Willing to use oral, implantable, transdermal or injectable contraceptives for 30 days prior to first vaccination and until 28 days after each vaccination
    • Willing to abstain from sexual intercourse or use another reliable form of contraception approved by the Investigator (eg, intrauterine device, female condom, and diaphragm with spermicide, cervical cap, use of condom by the sexual partner, or a sterile sexual partner) for study duration and until 28 days after vaccination
  • All female subjects must have a negative urine pregnancy test within 48 hours preceding receipt of each vaccination.
  • Comprehension of the study requirements, expressed availability for the required study period, and ability to attend scheduled visits and be contacted by telephone throughout the follow-up period

Exclusion Criteria:

  • Presence of significant uncontrolled medical or psychiatric illness (acute or chronic). This includes institution of new medical or surgical treatment, or a significant dose alteration for uncontrolled symptoms or drug toxicity within 3 months of screening and reconfirmed on Day 1 prior to vaccination
  • Positive serology for HIV-1 or HIV-2, or HBsAg or HCV antibodies
  • Pregnant or lactating female
  • Females who plan to become pregnant or plan to discontinue contraceptive precautions within 30 days prior to first vaccination and 28 days after each vaccination
  • Cancer, or treatment for cancer, within 3 years, excluding basal cell carcinoma or squamous cell carcinoma, which is allowed
  • Presence of any medical condition that may be associated with impaired immune responsiveness, including diabetes mellitus
  • Receipt (or history of receipt), during the preceding 3-month period, of any medications or other treatments that may adversely affect the immune system such as allergy injections, immune globulin, interferon, immunomodulators, cytotoxic drugs or other drugs known to be frequently associated with significant major organ toxicity, or systemic corticosteroids (oral or injectable). Inhaled and topical corticosteroids will be allowed.
  • Receipt or planned administration of a nonstudy vaccine within 30 days prior to vaccination or during the study. If a nonstudy vaccine has been administered, administration of study vaccine injection can be delayed and given as soon as allowable within the 30-day window, provided the nonstudy vaccine is not administered within 2 weeks prior to study enrollment. Immunization with Tetanus Toxoids Adsorbed for adult use (Td or Tdap) vaccine, on an emergency basis, up to 8 days before or at least 8 days after a dose of study vaccine will be allowed.
  • History of illicit drug or alcohol abuse within the previous 1 year or positive drug or alcohol screen
  • History of anaphylactic type reaction to injected vaccines
  • Receipt of any investigational product or nonregistered drug within the 30 days prior to vaccination or current enrollment in any investigational drug study or intent to enroll in such a study within the ensuing study period
  • Receipt or donation of blood or blood products 8 weeks prior to vaccination or planned receipt or donation during the study period
  • Acute disease, defined as the presence of a moderate or severe illness (as determined by the Investigator through medical history and physical examination) with or without fever, or an oral temperature of ≥38ºC, within 72 hours prior to vaccination. Study vaccine can be administered to persons with a minor illness, such as diarrhea or mild upper respiratory tract infection with or without low-grade fever. Vaccination can be delayed until the subject has recovered.
  • Any condition that, in the opinion of the Investigator, would interfere with the primary study objectives
Both
18 Years to 49 Years
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01290419
NVX 757.101
Yes
Novavax
Novavax
Not Provided
Study Director: D. Nigel Thomas, Ph.D. Novavax, Inc.
Principal Investigator: Dennis Ruff, MD Healthcare Discoveries d/b/a ICON Development Solutions
Novavax
March 2012

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