Group Study of the Safety of and Immune Response to a Single Dose of Bird Flu Vaccine (H7N3) in Healthy Adults

National Institute of Allergy and Infectious Diseases (NIAID)

Status and phase

Completed

Phase 1

Conditions

Influenza

Virus Diseases

Treatments

Biological: Live Influenza A Vaccine H7N3 (6-2) AA ca Recombinant (A/chicken/British Columbia/CN-6/2004 x A/Ann Arbor/6/60 ca)

Study type

Interventional

Funder types

NIH

Identifiers

NCT00853255

CIR 260

Details and patient eligibility

About

Over the past decade, avian influenza (AI) has become a major health concern. The development of safe and effective vaccines against avian strains that infect people is important. The purpose of this study is to determine the safety of and immune response of an investigational AI vaccine in healthy adults against the H7N3 strain of avian influenza.

Full description

The current pandemic risk associated with avian influenza H7N3 infection is significant, as an increasing number of humans are infected. H7 influenza transmission usually occurs in humans when they are exposed through direct contact to infected poultry or surfaces and objects contaminated by infected poultry feces. A pandemic occurs when a new influenza subtype emerges that infects humans, causes serious illness, and spreads easily between humans. The development of a safe and effective vaccine is necessary. The purpose of this study is to evaluate the safety and immunogenicity of a one-dose administration of the live, attenuated AI virus vaccine, H7N3 (6-2) AA ca Recombinant (A/chicken/British Columbia/CN-6/2004 x A/Ann Arbor/6/60 ca).

This study will last approximately 180 days. Participation in this study includes one 12-day hospital stay in an isolation unit at the University of Rochester Vaccine Evaluation Isolation Unit at St. Mary's Hospital in Rochester, NY. All participants will receive one dose of vaccine in nasal spray form at study entry. Participants will be admitted to the isolation unit 2 days prior to vaccination. A targeted physical exam, vital signs measurement, and nasal wash will occur daily following each vaccination until discharge. Participants will be discharged after two consecutive nasal washes on or after Day 7 are negative. Blood and urine collection will occur at selected timepoints throughout the study. Follow-up outpatient visits will occur approximately at Days 28, 56, and 180. A nasal wash and adverse events evaluation will occur at each follow-up visit.

Enrollment

20 patients

Sex

All

Ages

18 to 49 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Good general health
Available for the duration of the trial
For females, willing to use acceptable forms of contraception for the duration of the study. More information on this criterion can be found in the protocol.

Exclusion criteria

Clinically significant neurologic, heart, lung, liver, rheumatologic, autoimmune, or kidney disease
Behavioral or cognitive impairment or psychiatric disease that, in the opinion of the investigator, may affect study participation
Previously enrolled in an H7N3 influenza vaccine trial or in any study of an avian influenza vaccine
Seropositive to the H7N3 influenza A virus (serum hemagglutination inhibition [HI] titer greater than 1:8)
Illegal drug use or dependency determined by urine test
Medical, work, or family problems as a result of alcohol or illicit drug use within 12 months prior to study entry
History of severe allergic reaction
Allergy to oseltamivir
Asthma or reactive airways disease within 2 years prior to study entry
History of Guillain-Barre syndrome
HIV-infected
Hepatitis C virus infected
Positive for hepatitis B surface antigen (HBsAg)
Known immunodeficiency syndrome
Use of corticosteroids or immunosuppressive drugs within 30 days prior to vaccination. Participants who have used topical corticosteroids are not excluded.
Receipt of live vaccines within 4 weeks prior to study vaccination
Receipt of killed vaccines within 2 weeks prior to study vaccination
Absence of spleen
Receipt of blood products within 6 months prior to study vaccination
Current smoker unwilling to stop smoking for the duration of the study
Have traveled to the Southern Hemisphere within 14 days prior to study vaccination
Have traveled on a cruise ship within 14 days prior to study vaccination
Work in the poultry industry within 14 days prior to or after study vaccination
Other investigational vaccine or drug within 30 days prior to study vaccination
Allergy to eggs or egg products
Other condition that, in the opinion of the investigator, may interfere with the study
Pregnant or breastfeeding