Immunogenicity and Safety Trial of Adjuvanted and Non-adjuvanted Trivalent Influenza Vaccine in Tropical Africa

NCT ID: NCT01819155

Last Updated: 2013-10-22

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 296 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2013-04-30
• Study Completion Date: 2013-09-30

Brief Summary

This study will provide the Senegal Ministry of Health with data on the safety and immunogenicity of adjuvanted trivalent inactivated influenza vaccine (adjTIV) and full-dose seasonal non-adjuvanted trivalent inactivated influenza vaccine (TIV) in children. This data will inform future policy considerations for influenza vaccine. The study is not powered to detect significant differences between vaccines or groups, and no hypotheses are to be tested; therefore, immunogenicity and safety objectives are to be analyzed descriptively.

Detailed Description

The is a phase 2b, single-center, randomized, observer-blind, parallel group, placebo-controlled trial of the immunogenicity and safety of adjTIV and seasonal TIV among healthy children aged 6 months through 71 months in the town of Niakhar, Senegal. A total of 300 healthy children will be randomized in a 2:2:1 ratio of adjTIV to TIV to placebo. Each child will receive two doses of one of the three study vaccines, with each dose given 28 days apart. Each child will be followed closely for safety after each dose for the period from one month post-dose two to 3 months post-dose two. For determination of immune response to vaccination or background influenza infection, 3 mL of blood will be obtained at three time points: pre-vaccination, 28 days post-dose one (prior to receipt of dose two), and at 28 days post-dose two. Serum anti-influenza antibodies produced against virus strains contained in the vaccine will be detected using hemagglutination inhibition assay.

Conditions

Influenza

Keywords

influenza; influenza vaccine; immunogenicity; Africa; Senegal

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: QUADRUPLE

Study Groups

adjTIV

Children randomized to receive adjTIV

Group Type: EXPERIMENTAL

Adjuvanted seasonal trivalent inactivated influenza vaccine

Intervention Type: BIOLOGICAL

TIV

Children randomized to receive TIV

Group Type: EXPERIMENTAL

Seasonal trivalent inactivated influenza vaccine

Intervention Type: BIOLOGICAL

Placebo

Children randomized to receive Placebo

Group Type: PLACEBO_COMPARATOR

Saline (bacteriostatic 0.9% sodium chloride for injection)

Intervention Type: BIOLOGICAL

Interventions

Adjuvanted seasonal trivalent inactivated influenza vaccine

Intervention Type: BIOLOGICAL

Seasonal trivalent inactivated influenza vaccine

Intervention Type: BIOLOGICAL

Saline (bacteriostatic 0.9% sodium chloride for injection)

Intervention Type: BIOLOGICAL

Other Intervention Names

Fluad; VaxiGrip

Eligibility Criteria

Inclusion Criteria

• A male or female child at least 6 months of age and under 6 years of age (has not yet reached 72 months of age) at the enrollment visit.
• Free of obvious health problems, as established by the medical history and screening evaluations, including physical examination.
• Subject's parent or legal guardian is willing to provide written informed consent prior to the subject's first study vaccination.

Exclusion Criteria

• Known hypersensitivity to any component in adjTIV or TIV (which include egg protein) or placebo.
• Receipt of any non-study vaccine within two weeks prior to enrollment or refusal to postpone receipt of such vaccines until after the Day 56 visit.
• Previous receipt of any influenza vaccine.
• Hypersensitivity after previous administration of any vaccine.
• Acute illness accompanied by a body temperature of 37.5°C or greater (axillary measurement) within 14 days of enrollment visit. (Enrollment and administration of adjTIV, TIV, or placebo should be postponed until at least 14 days after recovery. Minor illnesses, such as mild upper respiratory infection, with an axillary temperature of <37.5°C, are not reason for exclusion or postponing study vaccination.)
• Any condition that, in the opinion of the investigator, would pose a health risk to the participant if he/she participates in the study or would interfere with the evaluation of the study objectives.

• Minimum Eligible Age: 6 Months
• Maximum Eligible Age: 71 Months
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Institut de Recherche pour le Developpement

OTHER_GOV

Sponsor Role: collaborator

Centers for Disease Control and Prevention

FED

Sponsor Role: collaborator

PATH

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Aldiouma Diallo, MD

Role: PRINCIPAL_INVESTIGATOR

Institut de Recherche pour le Developpement

John C Victor, PhD, MPH

Role: STUDY_DIRECTOR

PATH

Locations

Institut de Recherche pour le Développement

Niakhar, , Senegal

Countries

Senegal

References

Diallo A, Victor JC, Feser J, Ortiz JR, Kanesa-Thasan N, Ndiaye M, Diarra B, Cheikh S, Diene D, Ndiaye T, Ndiaye A, Lafond KE, Widdowson MA, Neuzil KM. Immunogenicity and safety of MF59-adjuvanted and full-dose unadjuvanted trivalent inactivated influenza vaccines among vaccine-naive children in a randomized clinical trial in rural Senegal. Vaccine. 2018 Oct 15;36(43):6424-6432. doi: 10.1016/j.vaccine.2018.08.032. Epub 2018 Sep 14.

Reference Type: DERIVED

PMID: 30224199 (View on PubMed)

Other Identifiers

MF59-TIV-SEN-01

Identifier Type: -

Identifier Source: org_study_id