A Safety and Immunogenicity Trial in Adults 65 Years of Age or Over to Prevent Influenza

NCT00706732 | Completed Phase 1

• 1 other identifier: AVX502-003
• Study Type: interventional
• Target: 28
• Locations: 1 country
• Sites: 1

Brief Summary

The objective of this study is to evaluate the safety of the vaccine and the immune response to the vaccine in healthy adult volunteers 65 years of age or older. Volunteers will be assigned by randomization to receive either the vaccine or an inactive substance (placebo) by injections in the arm on two occasions over one month. The study will last approximately 10 months and will have a total of 7 visits.

Conditions

Influenza

Keywords

Influenza; Flu; A/Wyoming/03/2003; Alphavirus

Outcome Measures

Primary Outcomes (1)

• Evaluate the safety of AVX502 in healthy adult volunteers 65 years of age or older via the frequency of systemic reactogenicity events, local vaccine reactions and Adverse Events

  28 weeks

Secondary Outcomes (1)

• Evaluate the immunogenicity of AVX502 in healthy adult volunteers 65 years of age and older via serum antibody concentration

  4 weeks after second dose of vaccine

Study Arms (4)

T1

ACTIVE COMPARATOR

Biological: AVX502

T2

ACTIVE COMPARATOR

Biological: AVX502

C1

PLACEBO COMPARATOR

Biological: Placebo

C2

PLACEBO COMPARATOR

Biological: Placebo

Interventions

AVX502 BIOLOGICAL

2 doses at 2e8 IU given at T=0 and T=4 weeks via the IM route

T1

Placebo BIOLOGICAL

2 doses of placebo given at T=0 and T=4 weeks via the IM route

C1

Eligibility Criteria

• Age: 65 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Older Adult (65+)

You may qualify if:

• Age 65 years of age or older
• Good general health without significant physical examination findings or clinically significant abnormal laboratory results
• Available to participate for entire study period
• Acceptable laboratory parameters
• Willingness to have blood stored for up to 10 years for use in additional assays to evaluate immune responses to influenza or the alphavirus vector if such assays become available
• Willingness to refrain from donating blood while participating in the study
• Willingness to delay receipt of 2008-2009 licensed influenza vaccination until after completing study visit 6 procedures (study week 8)
• Signed inform consent obtained before screening and before enrollment

You may not qualify if:

• Venous access deemed inadequate for th phlebotomy demands of the study
• Receipt of any other vaccine within 30 days prior to enrollment
• Use of any investigational agent within 30 days prior to enrollment
• Receipt of immunoglobulin or other blood products within 60 days prior to enrollment
• Use of cytotoxic medications within 6 months prior to enrollment
• Use of systemic corticosteroids within 6 months prior to enrollment (except that participants who have completed a course of prednisone, at up to 20 mg per day for up to 7 days, at least 1 month prior to enrollment are eligible for enrollment)
• History of serious adverse reactions to any vaccines, including anaphylaxis and related symptoms such as hives, respiratory difficulty, angioedema, or abdominal pain
• History of autoimmune disease or splenectomy
• History of malignancy within the last 3 years (except that participants with a diagnosis of basal cell carcinoma of the skin are eligible for enrollment)
• Psychiatric condition that may interfere with the ability to comply with the protocol requirements or to understand informed consent. Specifically excluded are persons with history of psychosis within the past 3 years or history of suicidal attempt or gesture within the past 3 years.
• History of medical, occupational, or family problems as a result of alcohol or illicit drug use during the past 12 months
• Any condition which leads the investigator to believe that the particpant cannot comply with the protocol requirements or that may place the participant at an unacceptable risk for further participation.

Sponsors & Collaborators

• AlphaVax, Inc.: lead

Study Sites (1)

Johnson County Clin-Trials

Lenexa, Kansas, 66219, United States

Location

Related Links

• AlphaVax, Inc.
• Johnson County Clin-Trials

MeSH Terms

Conditions

Influenza, Human

Condition Hierarchy (Ancestors)

Respiratory Tract Infections; Infections; Orthomyxoviridae Infections; RNA Virus Infections; Virus Diseases; Respiratory Tract Diseases

Study Officials

• Robert Olmsted, Ph.D.

  AlphaVax, Inc.

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: QUADRUPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
• Purpose: PREVENTION
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: June 26, 2008
• First Posted: June 30, 2008
• Study Start: June 1, 2008
• Primary Completion: September 1, 2008
• Study Completion: March 1, 2009
• Last Updated: July 12, 2012

Record last verified: 2012-07

Locations

US (1)