Phase 3 Trial of Serbian Seasonal Influenza Vaccine

Phase 3

Completed

Conditions: Influenza

Interventions: Other: Placebo
Biological: Vaccine

Registration Number: NCT02935192

Lead Sponsor: Institute of Virology, Vaccines and Sera, Torlak

Brief Summary: A Phase 3, double-blind, randomized, placebo-controlled trial of a seasonal, trivalent, split, inactivated influenza vaccine produced by InstituteTorlak.

Detailed Description: This is a phase 3, double-blind, randomized, placebo- controlled trial with two groups of participants to receive seasonal trivalent split, inactivated influenza vaccine (A/H1N1; A/H3N2 and B) or placebo (phosphate buffered saline). A total of about 480 healthy male and female adults 18 through 65 years of age; 320 participants will be randomized to receive vaccine and160 will receive placebo (a 2:1 ratio). At least 25% of the participants (N=120) will be \>/= 45 years of age (80 vaccine and 40 placebo recipients).

Safety will be assessed in all participants through Day 91. Immunogenicity will be assessed in serum samples obtained at baseline and 21 days after vaccination in a subset of at least 100 individuals randomized to study vaccine and 50 placebo recipients.

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 480

Inclusion Criteria

Aged 18 to 65 years on the day of screening/enrollment.
Literate (by self-report) and willing to provide written informed consent.
Able to attend all scheduled visits and to comply with all trial procedures.
Healthy or medically stable, as established by medical history and physical examination. For individuals with medical conditions, symptoms/signs, if present must be stable under control or unchanged for the past three months. If medication is used to treat the condition, the medication dose must have been stable for at least one month preceding vaccination.

For female participants:

Not breast feeding, non-pregnant (based on negative urine pregnancy test) and no plan to become pregnant up to Day 22.
Women who are not surgically sterile (hysterectomy or tubal ligation) or post-menopausal for more than one year must be willing to use effective contraceptive method to prevent pregnancy until three weeks (Day 22) after vaccination. Effective methods include intrauterine device, hormonal contraceptives (oral, injectable, patch, implant, ring) or double barrier contraceptives (condom or diaphragm with spermicide). Women with credible history of abstinence may be enrolled at the discretion of the investigator.

Exclusion Criteria

Participation in another clinical trial involving any therapy within the previous three months or planned enrollment in such a trial during the period of this study.
Receipt of influenza vaccine in the last 10 months.
Receipt of any non-study vaccine within four weeks prior to enrollment or refusal to postpone receipt of such vaccines until after the Day 22 visit.
Receipt of immune globulin or other blood products within three months prior to study enrollment or planned receipt of such products prior to the Day 22 visit.
Known or suspected congenital or acquired immunodeficiency.
Chronic administration (defined as more than 14 consecutively-prescribed days) of immunosuppressants or other immune-modulating therapy within six months prior to study enrollment. (For corticosteroids, this means prednisone or equivalent, ≥ 0.5 mg per kg per day; topical steroids are allowed.)
Unstable illness by history or physical examination that in the opinion of the investigator, might interfere with the conduct or results of the study or pose additional risk to the participant.
Hypersensitivity after previous administration of any vaccine.
Suspected or known hypersensitivity to any of the study vaccine components, including chicken or egg protein or antibiotics.
Bleeding disorder or receipt of anticoagulants in the three weeks preceding enrollment.
Known active tuberculosis or symptoms of active tuberculosis, regardless of cause (self-report).
Current alcohol or drug addiction that in the opinion of the Investigator, might interfere with the ability to comply with trial procedures.
History of Guillain-Barré Syndrome.
Neoplastic disease or any hematologic malignancy. Allowed: localized skin or prostate cancer that is no longer being treated and is stable at the time of vaccination and participants who have a history of neoplastic disease and who have been disease free for ≥ 5 years.
Any condition that, in the opinion of the investigator, would increase the health risk to the participant if he/she participates in the study, or would interfere with the evaluation of the study objectives.

Study & Design

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Placebo Arm	Placebo	Phosphate buffered saline
Vaccine Arm	Vaccine	Seasonal trivalent split, inactivated influenza vaccine

Primary Outcome Measures

Name	Time	Method
Number of Participants With Solicited Local Adverse Events (Local Reactogenicity)	5-day period (Days 1-5) post-vaccination	Number of subjects reporting one or more solicited local reactions (redness/erythema, swelling/induration, pain, and tenderness) at the injection site post-vaccination with study vaccine or placebo
Number of Participants With Solicited Adverse Events (Local & Systemic Reactogenicity)	30-minute post-vaccination period	Number of participants experiencing one or more solicited local AEs, including redness /erythema, swelling / induration and pain
Number of Participants With Solicited Systemic Adverse Events (Systemic Reactogenicity)	5-day period (Days 1-5) post-vaccination	Number of subjects reporting one or more solicited systemic reactions (fever, fatigue/malaise, muscle aches, joint aches, chills, nausea, vomiting, and headache) post-vaccination with study vaccine or placebo.
Number and Percentage of Seroconverted Subjects	Day 22	Seroconversion is defined as a serum HAI antibody titer meeting the following criteria: * Pre-vaccination titer \<1:10 and a post-vaccination titer measured on Day 22 of ≥1:40; or * Pre-vaccination titer ≥1:10 and at least a four-fold increase in post-vaccination measured on Day 22. Measured against each of the 3 antigens
Number and Percentage of Participants With a HAI Antibody Titer ≥1:40 (Seroprotection)	Day 1 and Day 22	Seroprotective Titers is considered as HAI antibody Titre ≥1:40; measured for each of the 3 antigens
Geometric Mean Fold Rises (GMFRs) of Serum HAI Antibodies	Day 1 and Day 22	GMFR calculated as GMT for of Serum HAI Antibodies Post-vaccination/Pre-vaccination; measured for each of the 3 antigens
Number of Participants With Unsolicited Adverse Events	Within 21 days post vaccination	Unsolicited AEs occurring in 1% or more of study participants; includes events irrespective of causality
Number of Participants With Serious Adverse Events (SAE)	Over the entire study period (Day 91)	Number of participants reporting one or more of all anticipated and unanticipated serious adverse events, grouped by organ system, with number and frequency of such events in each arm/group of the clinical study.
Geometric Mean Titers (GMTs) of Serum HAI Antibodies	Day 1 and Day 22	Serum HAI Antibodies GMTs Pre- (Day 1) and Post-vaccination (Day 22); measured for each of the 3 antigens

Secondary Outcome Measures

Name	Time	Method

Trial Locations

Locations (6): Institute for Students' Healthcare
🇷🇸
Belgrade, Serbia
Institute of Health Care of Workers of the Ministry of Internal Affairs
🇷🇸
Belgrade, Serbia
General Hospital Vrsac
🇷🇸
Vršac, Serbia
Clinical Center of Serbia: Clinic for Infectious and Tropical Diseases
🇷🇸
Belgrade, Serbia
Clinical Center of Serbia: Clinic for Pulmonology
🇷🇸
Belgrade, Serbia
Jevremova Special gynecology hospital with maternity
🇷🇸
Belgrade, Serbia