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Effect of the Interferon Alpha Citizen by Sub-Lingual Way on the Humoral Immunizing Answer (GP-INFA)

Primary Purpose

Influenza Infection

Status
Terminated
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
vaccine
Placebo
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Influenza Infection focused on measuring Influenza vaccine, interferon, adjuvant, the elderly

Eligibility Criteria

75 Years - undefined (Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Subjects aged 75 or more, -institutionalized-
  • Subjects who were informed of the objectives of the study and who have given their written consent.
  • Subjects who have received at least one prior influenza vaccination in the previous 5 years.
  • Subjects who should be vaccinated against influenza during the 2005 vaccination campaign.

Exclusion Criteria:

  • Individuals with severe disease, including neoplasia, autoimmune disease, or type I diabetes
  • concomitant treatment with glucocorticoid or immunosuppressive drugs splenectomy or tonsillectomy
  • or incapacity to open the mouth

Sites / Locations

  • Assistance Publique-Hôpitaux de Paris, Groupe Hospitalier Broca-La Rochefoucauld, Service de Gérontologie 1

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

1

2

Arm Description

IFNalpha 2b

Placebo

Outcomes

Primary Outcome Measures

Percentage of subjects presenting an increase > 4 fold of antiH1N1 or antiH3N2 or anti-B haemagglutination inhibition antibody titer, 3 weeks following influenza vaccination.

Secondary Outcome Measures

geometric mean of haemagglutination antibody titer obtained at day 21 with or without IFNa
influenza virus strain-specific IgG total, IgG2a, IgG2a/IgG1 ratio, secretory IgA responses at day 21 in each group .
influenza virus strain-specific secretory IgA anti-influenza antibody titers in saliva 14 and 21 days following vaccination.
evaluation of individual response to IFNa treatment
levels of serologic alpha interferon and of anti- alpha -interferon at day 21.
Percentage of patients maintaining protective antibody titers 3 and 6 months following vaccination.
Predictive factors of vaccine response (age, total lymphocyte cell count, CD4 cell count…)
Evaluation of cellular vaccine response in a subgroup of subjects.

Full Information

First Posted
March 26, 2008
Last Updated
March 28, 2008
Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Orakine Ltd, Dublin, Ireland
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1. Study Identification

Unique Protocol Identification Number
NCT00647465
Brief Title
Effect of the Interferon Alpha Citizen by Sub-Lingual Way on the Humoral Immunizing Answer
Acronym
GP-INFA
Official Title
Randomized Double-Blind Placebo Controlled Study Evaluating the Effect of Sublingual Administration of IFNa on the Immune Response to Influenza Vaccination in Subjects Aged 75 or More.
Study Type
Interventional

2. Study Status

Record Verification Date
November 2005
Overall Recruitment Status
Terminated
Why Stopped
End of the study
Study Start Date
October 2005 (undefined)
Primary Completion Date
May 2006 (Actual)
Study Completion Date
March 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Orakine Ltd, Dublin, Ireland

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Influenza vaccination reduces the morbidity and mortality associated with influenza infection in at risk groups including the elderly and individuals with an impaired immune response, but is not totally protective in all recipient. Cytokines including type I interferons are known to play a key role in the innate immune response to virus infection and in the induction of the primary adaptive-immune response. Thus, we evaluated the safety of sublingual administration of IFNa and its effect on immune response to influenza vaccination in a randomized double-blind placebo controlled study in elderly institutionalized individuals.
Detailed Description
The protection afforded by the commonly used influenza sub-unit vaccines is thought to be due principally to the production of antibodies to viral haemagglutinin. The haemagglutination inhibitory (HAI) antibody titer is generally used as a surrogate marker of protection and a HAI antibody titer of 1:40 or greater is considered to confer protection. This is attained, however, in only 50% of elderly subject. Thus, there is an unmet need for an effective non-toxic adjuvant capable of enhancing the antibody response to influenza and other vaccines. Type I IFNs have been shown to induce B-lymphocytes to differentiate into antibody producing plasma cells and to be necessary for the production of both specific and polyclonal IgGs in response to influenza infection. Furthermore, type I IFNs increase the primary antibody response to a soluble antigen in vivo, and increase the production of all IgG sub-classes. Type I IFNs play a key role in adjuvant-induced Th1 responses. Thus, we evaluated the safety of sublingual administration of IFNa and its effect on immune response to influenza vaccination.Institutionalized subjects, aged 75 or more, were randomly assigned to two groups to receive in a double-blind fashion either 107 IU of Intron ATM in 1 ml of isotonic saline or 1 ml of saline alone (placebo) administered sublingually. Interferon or placebo were retained in the mouth for at least 30 seconds prior to ejection. All subjects were then vaccinated, within 30 minutes, with a single intramuscular injection (im) of influenza vaccine (InfluvacTM, Solvay Pharma, France). The primary objective of this study is to compare the immunogenicity percentage of subjects who increased up to 4 fold their HAI antibody titer at day 21) obtained in the IFN treated group relative to the placebo treated group. The secondary objectives are to compare mean HAI antibodies titers obtained in the two groups at day 21 ; specific IgG, IgG2a, IgG2a/IgG1 ratio and secretory IgA titers in the 2 groups; specific secretory IgA titers in saliva; durability of protective HAI antibodies titers 3 and 6 months after the vaccination and the safety of sublingual administration of IFNa.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Influenza Infection
Keywords
Influenza vaccine, interferon, adjuvant, the elderly

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
140 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
IFNalpha 2b
Arm Title
2
Arm Type
Placebo Comparator
Arm Description
Placebo
Intervention Type
Drug
Intervention Name(s)
vaccine
Other Intervention Name(s)
Influenza vaccination
Intervention Description
IFNalpha 2b
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
Percentage of subjects presenting an increase > 4 fold of antiH1N1 or antiH3N2 or anti-B haemagglutination inhibition antibody titer, 3 weeks following influenza vaccination.
Time Frame
21 days
Secondary Outcome Measure Information:
Title
geometric mean of haemagglutination antibody titer obtained at day 21 with or without IFNa
Time Frame
21 days
Title
influenza virus strain-specific IgG total, IgG2a, IgG2a/IgG1 ratio, secretory IgA responses at day 21 in each group .
Time Frame
21 days
Title
influenza virus strain-specific secretory IgA anti-influenza antibody titers in saliva 14 and 21 days following vaccination.
Time Frame
21 days
Title
evaluation of individual response to IFNa treatment
Time Frame
21 days
Title
levels of serologic alpha interferon and of anti- alpha -interferon at day 21.
Time Frame
21 days
Title
Percentage of patients maintaining protective antibody titers 3 and 6 months following vaccination.
Time Frame
3 months and 6 months after
Title
Predictive factors of vaccine response (age, total lymphocyte cell count, CD4 cell count…)
Time Frame
21 days
Title
Evaluation of cellular vaccine response in a subgroup of subjects.
Time Frame
21 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Subjects aged 75 or more, -institutionalized- Subjects who were informed of the objectives of the study and who have given their written consent. Subjects who have received at least one prior influenza vaccination in the previous 5 years. Subjects who should be vaccinated against influenza during the 2005 vaccination campaign. Exclusion Criteria: Individuals with severe disease, including neoplasia, autoimmune disease, or type I diabetes concomitant treatment with glucocorticoid or immunosuppressive drugs splenectomy or tonsillectomy or incapacity to open the mouth
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Frederic Bloch, MD, PhD
Organizational Affiliation
Assistance Publique-Hôpitaux de Paris, Groupe Hospitalier Broca-La Rochefoucauld, Service de Gérontologie 1 AP-HP
Official's Role
Principal Investigator
Facility Information:
Facility Name
Assistance Publique-Hôpitaux de Paris, Groupe Hospitalier Broca-La Rochefoucauld, Service de Gérontologie 1
City
Paris
ZIP/Postal Code
75005
Country
France

12. IPD Sharing Statement

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Effect of the Interferon Alpha Citizen by Sub-Lingual Way on the Humoral Immunizing Answer

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