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Clinical Trials/NCT01897701
NCT01897701
Completed
Phase 1

A Phase 1 Randomized, Observer-Blinded, Dose-Ranging Study to Evaluate the Immunogenicity and Safety of Monovalent A/Anhui/1/2013 (H7N9) Virus-Like Particle (VLP) Avian Influenza Antigen (Recombinant) in Healthy Adults With and Without Adjuvant 1

Novavax3 sites in 1 country280 target enrollmentJuly 2013
ConditionsAvian Influenza

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Avian Influenza
Sponsor
Novavax
Enrollment
280
Locations
3
Primary Endpoint
Assessment of Safety
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

This is a randomized, observer-blinded, placebo-controlled trial in adults ≥18 years old. Randomization will be stratified by age (18 to 49 years and ≥50 years) and by prior influenza immunization within the past three months. Proportions of subjects in the various strata will not be pre-specified; rather, the goal will be to achieve an approximately equal distribution of subjects with these characteristics across the various treatment groups.

Treatments will comprise two identical IM doses at a 21-day interval (Day 0 and Day 21), in alternate deltoids. For each subject, study follow-up will span approximately 385 days total, or approximately 13 months from the first dose.

Registry
clinicaltrials.gov
Start Date
July 2013
End Date
August 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Novavax
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Subjects must meet all of the following to be eligible for participation in the study:
  • Healthy adult male or female, ≥18 years of age,
  • Willing and able to give informed consent prior to study enrollment,
  • Able to comply with study requirements, and
  • Women of childbearing potential must have a negative urine pregnancy test prior to each vaccination, will be advised through the Informed Consent process to avoid becoming pregnant over the duration of the study, and must assert that they will employ an effective form of birth control for the duration of the study. Acceptable forms of birth control are: credible history of continuous abstinence from heterosexual activity or prior surgical sterilization, hormonal contraceptives (oral, injectable, implant, patch, ring), barrier contraceptives (condom or diaphragm), and intrauterine device (IUD). Women with an adequately documented history of surgical sterility, or ≥50 years of age and without menses for ≥ 1 year are exempt from urine pregnancy testing.

Exclusion Criteria

  • Subjects meeting any of the following criteria are not eligible for participation in the study.
  • Any ongoing, symptomatic acute or chronic illness requiring medical or surgical care.
  • Asymptomatic conditions or findings (e.g., mild hypertension, dyslipidemia) that are not associated with evidence of end-organ damage are not exclusionary provided that they are being appropriately managed and are clinically stable (i.e., unlikely to result in symptomatic illness within the time-course of this study) in the opinion of the investigator.
  • Note that illnesses or conditions may be exclusionary, even if otherwise stable, due to therapies used to treat them (see exclusion criteria 2, 5, 7, 8).
  • Participation in research involving investigational product (drug / biologic / device) within 45 days before planned date of first vaccination.
  • History of a serious reaction to prior influenza vaccination.
  • History of Guillain-Barré Syndrome (GBS) within 6 weeks following a previous influenza vaccine.
  • Received any vaccine in the 4 weeks preceding the study vaccination; or any A(H7N9) avian influenza vaccine at any time.
  • 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.

Outcomes

Primary Outcomes

Assessment of Safety

Time Frame: Day 0 to Day 384

Number (and percentages) of subjects with solicited local and systemic AEs over the seven days post-injection and all adverse events, solicited and unsolicited, including adverse changes in clinical laboratory parameters, over 35 days post-first injection. Significant New Medical Conditions, Medically Attended Events and Serious Adverse Events will be collected for one year post-second injection.

Immunogenicity as assessed by hemagglutination-inhibiting (HAI) antibody titers against the vaccine-homologous A/Anhui/1/13 (H7N9) virus.

Time Frame: Day 0 to Day 384

* Geometric mean titer (GMT) * Geometric mean ratio (GMR) * Seroconversion rate (SCR) * Seroresponse rate (SRR)

Secondary Outcomes

  • Immunogenicity as assessed by neuraminidase-inhibiting antibodies to N9.(Day 0 to Day 384)

Study Sites (3)

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