Safety and Immunogenicity Study of an Inactivated Influenza Vaccine (Split Virus, Vero Cell Derived)

Ology Bioservices

Status and phase

Completed

Phase 2

Phase 1

Conditions

Influenza

Treatments

Biological: Inactivated seasonal influenza vaccine (split virus, vero cell derived)

Biological: Inactivated seasonal influenza vaccine (split virus, egg derived) [licensed control vaccine]

Study type

Interventional

Funder types

Industry

Identifiers

NCT00424086

720601

Details and patient eligibility

About

The objective of this study is to assess the safety, tolerability and immunogenicity of a Split Virus, Vero Cell derived, Seasonal Influenza Vaccine (VCIV) in comparison to a Licensed Egg Derived, Split Virus, Seasonal Influenza Vaccine (EIV) in healthy subjects 18 years of age and older.

Approximately 1000 subjects will be randomly assigned in a 3:1 ratio to receive a single injection of VCIV or EIV. Subjects will be monitored for 180 days following vaccination for occurrence of adverse reactions and for antibody response to the vaccine.

Enrollment

1,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Male and female subjects who

Are 18 to 49 years of age (inclusive) on the day of screening (Stratum A)
Are 50 years of age or older on the day of screening (Stratum B)
Have an understanding of the study, agree to its provisions, and give written informed consent prior to study entry
Are clinically healthy (in a physical condition such that the physician would have no reservations administering influenza vaccine outside the scope of a clinical study)
Are physically and mentally capable of participating in the study
Agree to keep a daily record of symptoms
If female and capable of bearing children, have a negative urine pregnancy test result within 24 hours of the vaccination on Study Day 0 and agree to employ adequate birth control measures. For the purposes of this study adequate birth control measures incorporate 2 types of the following FDA approved birth control measures through 60 days after vaccination:
- Hormonal types of birth control (such as implants, birth control pills, patches or other methods) or an intrauterine device, AND
- An additional barrier type of birth control measure (i.e., condoms, diaphragms, cervical caps, etc.)

Exclusion criteria

Subjects who

Have previously been vaccinated against influenza with vaccine formulated for the 2006/2007 influenza season
Have an oral temperature >=37.5°C at the time of vaccination on Day 0 (see note below)
Have Type I diabetes
Have a Body Mass Index >35
Have hypertension at screening (with or without medication) that is graded as greater than Stage 1 defined as a systolic pressure >159 or diastolic pressure >99 while seated and at rest (measurement may be repeated twice before subject is absolutely excluded)
Have clinically significant abnormal clinical laboratory values at screening
Have clinically significant electrocardiographic abnormalities at screening
Test positive for Human Immunodeficiency Virus(HIV), Hepatitis B Surface Antigen (HbsAg) or Hepatitis C Virus (HCV)
Have a history of cardiovascular disease that required hospitalization
Have a history of immunodeficiency or autoimmune diseases
Have a history of arthritis (joint swelling, tenderness, warmth or erythema) on more than one occasion, not related to trauma (including running) or any episode of non-trauma related arthritis within the previous 6 months
Suffer from active neoplastic disease or have a history of hematologic malignancy
Suffer from a disease or are undergoing a form of treatment that can be expected to influence immune response. Such treatment includes, but is not limited to systemic or high dose inhaled (>800 μg/day of beclomethasone dipropionate or equivalent) corticosteroids, radiation treatment or other immunosuppressive or cytotoxic drugs
Have a history of inflammatory or degenerative neurological disease (e.g. Guillain Barré, multiple sclerosis)
Have received any vaccination within 2 weeks prior to vaccination in this study
Have received a blood transfusion or immunoglobulins within 30 days prior to vaccination in this study
Have donated blood or plasma within 30 days prior to vaccination in this study
Have a history of any vaccine related contraindicating event (e.g., anaphylaxis, allergy to eggs, allergy to components of the test or comparator vaccine, other known contraindications)
Have a rash, dermatologic condition or tattoos which may interfere with injection site reaction rating
Have a positive urine drug screen (unless the detected drug is currently prescribed by a licensed health care provider and the continued administration of the drug would not otherwise exclude the subject from participation)
Were administered an investigational drug within 6 weeks prior to study entry
Are concurrently participating in a clinical study that Inactivated Influenza Vaccine (Split Virus, Vero Cell Derived)includes the administration of an investigational product
Are a member of the team conducting this study
Are in a dependent relationship with the study investigator. Dependent relationships include close relatives (i.e., children, partner/spouse, siblings, parents) as well as employees of the investigator
If female, are pregnant or lactating.

NOTE: If all other inclusion/exclusion criteria are met, a subject with a temperature >=37.5°C on Day 0 may be included in the study at a repeat visit provided:

They do not have an oral temperature >=37.5°C at the repeat visit,
The repeat visit is no more than 5 calendar days after the initial Day 0 visit,
The repeat visit is no more than 21 calendar days after all other screening procedures are completed,
Subjects are still being recruited at the study site.