Intradermal Influenza Vaccine in the Young

Influenza Viral Infections Clinical Trial

Official title:

Intradermal Trivalent Influenza Vaccine in Young Adults, a Double-blind Randomized Controlled Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02103023
• Other study ID #: UW 14-016
• Status: Completed
• Phase: Phase 3
• First received: March 28, 2014
• Last updated: December 3, 2014
• Start date: March 2014
• Est. completion date: November 2014

Study information

• Verified date: December 2014
• Source: The University of Hong Kong
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Influenza poses a heavy burden to our health service. The WHO estimates that seasonal influenza causes 250,000-500,000 deaths worldwide each year. Various strategies including intradermal vaccination and new vaccine adjuvants have been shown to improve immunogenicity. Recently, imiquimod, a synthetic Toll-like receptor 7 (TLR7) agonist useful for the treatment of DNA virus infection, have been shown to improve vaccine immunogenicity against influenza virus in mouse model. The objective of this prospective double-blind randomized controlled trial is to evaluate the effect and safety of topical treatment with imiquimod immediately before intradermal influenza vaccination in healthy young adults.

Description:

Influenza poses a heavy burden to our health service. Seasonal, zoonotic and pandemic influenza are constant global threats. The WHO estimates that seasonal influenza causes 250,000-500,000 deaths worldwide each year, with an even higher mortality during the pandemic periods. Moreover zoonotic influenza such as the avian-origin H5N1 and more recently the H7N9 influenza are associated with a much higher mortality than seasonal influenza. Vaccine immunogenicity among elderly individuals is also suboptimal due to immunosenescence. Various strategies including intradermal vaccination and new vaccine adjuvants have been shown to improve immunogenicity.

Recently, imiquimod, a synthetic Toll-like receptor 7 (TLR7) agonist useful for the treatment of DNA virus infection, have been shown to improve vaccine immunogenicity against influenza virus in both mouse model. The objective of this prospective double-blind randomized controlled trial is to evaluate the effect and safety of topical treatment with imiquimod immediately before intradermal influenza vaccination. Our a priori hypothesis is that imiquimod pretreatment would expedite and augment the immunogenicity of influenza vaccination.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 160
• Est. completion date: November 2014
• Est. primary completion date: November 2014
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 30 Years

Eligibility

Inclusion Criteria:

• All adult patients at the age of 18-30 years and given written informed consent

• Subjects must be available to complete the study and comply with study procedures.

• Willingness to allow for serum samples to be stored beyond the study period, for potential additional future testing to better characterize immune response.

Exclusion Criteria:

• Clinically significant immune-related diseases or significant recent co-morbidities

• Inability to comprehend and to follow all required study procedures

• History or any illness that might interfere with the results of the study or pose additional risk to the subjects due to participation in the study

• Have received trivalent influenza vaccine within the same year

• Have a recent history (documented, confirmed or suspected) of a flu-like disease within a week of vaccination.

• Have a known allergy to eggs or other components of the Study Vaccines (including gelatin, formaldehyde, octoxinol, thimerosal, and chicken protein), or history of any anaphylaxis, serious vaccine reactions, to any excipients.

• Have a positive urine or serum pregnancy test within 24 hours prior to vaccination, or women who are breastfeeding.

• Female of childbearing potential, not using any acceptable contraceptive methods for at least 2 months prior to study entry or that do not plan to use acceptable birth control measures during the first 3 weeks after vaccination.

• Have immunosuppression as a result of an underlying illness or treatment, or use of anticancer chemotherapy or radiation therapy (cytotoxic) within the preceding 36 months.

• Have an active neoplastic disease or a history of any hematologic malignancy.

• Have long-term use of glucocorticoids including oral, parenteral or high-dose inhaled steroids (>800 mcg/day of beclomethasone dipropionate or equivalent) within the preceding 6 months. (Nasal and topical steroids are allowed).

• Have a history of receiving immunoglobulin or other blood product within the 3 months prior to vaccination in this study.

• Have known active human immunodeficiency virus (HIV), Hepatitis C infection or autoimmune hepatitis and cirrhosis.

• Received an experimental agent (vaccine, drug, biologic, device, blood product, or medication) within 1 month prior to vaccination in this study or expect to receive an experimental agent during this study. Unwilling to refuse participation in another clinical study through the end of this study.

• History of progressive or severe neurological disorders Have received any licensed vaccines within 4 weeks or inactivated licensed vaccines within 2 weeks prior to vaccination in this study or plan receipt of such vaccines within 21 days following the second vaccination (only exception being unadjuvanted seasonal influenza vaccines which are allowed until 1 week prior to and after 1 week study vaccinations).

• Axillary temperature = 38°C or oral temperature = 38.5°C within 3 days of intended study vaccination

• Surgery planned during the study period that in the Investigator's opinion would interfere with the study visits schedule

• Have a history of alcohol or drug abuse in the last 5 years.

• Have a history of Guillain-Barré Syndrome. Have any condition that the investigator believes may interfere with successful completion of the study.

Related Conditions & MeSH terms

• Influenza Viral Infections
• Influenza, Human
• Virus Diseases

Intervention

Drug:
• Imiquimod ointment
5% 250mg imiquimod ointment
• Aqueous cream
aqueous cream

Biological:
• Intradermal influenza vaccine
intradermal trivalent influenza vaccine (Intanza15)
• Intramuscular influenza vaccine
intramuscular trivalent influenza vaccine (Vaxigrip)

Locations

Country	Name	City	State
China	The University of Hong Kong, Queen Mary Hospital	Hong Kong	Hong Kong

Sponsors (1)

Lead Sponsor	Collaborator
The University of Hong Kong

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Seroconversion rate	Hemagglutination inhibition assay	Day 7
Secondary	Seroprotection rate	Hemagglutination inhibition assay	Day 7
Secondary	GMT fold increase	Hemagglutination inhibition assay	Day 7
Secondary	GMT	Microneutralization antibody assay	Day 7
Secondary	Seroconversion rate	Hemagglutination inhibition assay	Day 21
Secondary	Seroprotection rate	Hemagglutination inhibition assay	Day 21
Secondary	GMT fold increase	Hemagglutination inhibition assay	Day 21
Secondary	GMT	Microneutralization antibody assay	Day 21
Secondary	Adverse events	Solicited local and systemic adverse reactions monitored from time of vaccination till day 7.	Day 7