A(H7N9) VLP Antigen Dose-Ranging Study With Matrix-M1™ Adjuvant

Influenza (Pandemic) Clinical Trial

Official title:

A Phase I/II Randomized, Observer-Blinded, Dose-Ranging Study to Evaluate the Immunogenicity and Safety of Monovalent A/Anhui/1/13 (H7N9) Virus-Like Particle (VLP) Avian Influenza Antigen (Recombinant) in Healthy Adults With and Without Matrix-M1™

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02078674
• Other study ID #: FLU-MI7A-201
• Status: Completed
• Phase: Phase 1/Phase 2
• First received: March 3, 2014
• Last updated: September 20, 2016
• Start date: March 2014
• Est. completion date: July 2015

Study information

• Verified date: September 2016
• Source: Novavax
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug AdministrationUnited States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

This is a randomized, observer-blinded, placebo-controlled trial in adults 18 to 64 years old. Randomization will be stratified by age (18 to 49 years and 50 to 64 years) and by prior influenza immunization within the past three months. Subjects 18 to 49 years of age will comprise ~67% of subjects in each treatment group, and the balance will comprise subjects 50 to 64 years.

Each subject will receive two identical IM doses of test article 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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 610
• Est. completion date: July 2015
• Est. primary completion date: July 2015
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 64 Years

Eligibility

Inclusion Criteria:

1. Healthy adult male or female, 18 to 64 years of age,

2. Willing and able to give informed consent prior to study enrollment,

3. Able to comply with study requirements, and

4. Women of child-bearing potential must have a negative urine pregnancy test prior to each vaccination, and 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 will be excluded if they meet any of the following criteria:

1. 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.

• Acute or chronic illnesses or conditions which may be reasonably predicted to become symptomatic if treatment were withdrawn or interrupted are exclusionary, even if stable.

• Note that illnesses or conditions may be exclusionary, even if otherwise stable and clinically minor, due to therapies used to treat them (see exclusion criteria 3, 5, 8, 9).

2. Any grade 1 or higher (as based on the Toxicity Grading Scale [TGS]) abnormality in ALT, AST, alkaline phosphatase, total bilirubin, blood urea nitrogen, or creatinine levels.

3. Any grade 2 or higher (as based on the TGS) vital sign or clinical laboratory abnormality not specified in criterion 2 above. Note that any abnormal vital sign may be repeated at the Investigator's discretion.

4. Participation in research involving investigational product (drug / biologic / device) within 45 days before planned date of first vaccination.

5. History of a serious reaction to prior influenza vaccination.

6. History of Guillain-Barré Syndrome (GBS) within 6 weeks following a previous influenza vaccine.

7. Received any vaccine in the 4 weeks preceding the study vaccination; or any A(H7N9) avian influenza vaccine at any time.

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

9. 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.

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

11. 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).

12. Known disturbance of coagulation.

13. Women who are pregnant or breastfeeding, or plan to become pregnant during the study.

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

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Prevention

Related Conditions & MeSH terms

• Influenza (Pandemic)
• Influenza, Human

Intervention

Biological:
• Monovalent Avian Influenza VLP (H7N9)

• Matrix-M1™ adjuvant

• Placebo

Locations

Country	Name	City	State
United States	Regional Clinical Research, Inc.	Endwell	New York
United States	Advanced Clinical Research	Meridian	Idaho
United States	Miami Research Associates	Miami	Florida
United States	Coastal Carolina Research	Mt. Pleasant	South Carolina
United States	Diablo Clinical Research	Walnut Creek	California

Sponsors (2)

Lead Sponsor	Collaborator
Novavax	Department of Health and Human Services

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Assessment of Safety	Counts (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 42 days post-first injection.; In addition, MAEs, SAEs, and SNMCs will be collected for one year.	Day 0 to Day 384	Yes
Primary	Immunogenicity as assessed by hemagglutination-inhibiting (HAI) antibody titers against the vaccine-homologous A/Anhui/1/13 (H7N9) virus.	Geometric mean titer (GMT) Geometric mean ratio (GMR) Seroconversion rate (SCR) Seroresponse rate (SRR)	Day 0 to Day 384	No
Secondary	Immunogenicity as assessed by neuraminidase-inhibiting antibodies to N9.		Day 0 to Day 384	No

External Links

•   Novavax, Inc