Standard-dose Versus High-dose Flu Vaccine in Solid Organ Transplant.

Phase 4

Completed

• Conditions: Transplantation Infection; Influenza, Human
• Interventions: Biological: influenza trivalent inactive vaccine; Biological: influenza trivalent inactive vaccine high dose

• Registration Number: NCT01808456
• Lead Sponsor: Inova Health Care Services

Brief Summary

Influenza infection in recipients of solid organ transplants recipients while on maintenance immunosuppressant therapy is associated with increased morbidity and mortality. Although influenza vaccination is recommended in these high-risk patients, safety and immunogenicity of commercially available different strengths of influenza vaccine have not been established.

The primary study objective is to determine the safety and immunogenicity of Fluzone and Fluzone High-Dose, with a secondary objective to determine the tolerability and efficacy of two different strengths of trivalent influenza vaccine (TIV, flu vaccine). Both vaccines are commercially available for use in the general population. Fluzone is approved for use in 6 months of age and older, and Fluzone High-Dose is approved for use in 65 years of age and older.

This is an exploratory, open-label, parallel group, observer blinded, prospective study. All recipients of kidney, lung, heart transplants who attend for post-transplant follow-up, at least 30-days after transplantation at Inova Fairfax Hospital Transplant Center will be eligible for enrollment.

Enrolled patients will be followed for three months (a total of 4 visits) following enrollment and randomization: day 0 (enrollment) and follow-up visits at weeks 1, 4, 8, and 12.

Detailed Description

A potential strategy to enhance immune responses to influenza vaccine in this patient population could be to use different strengths of TIV. One of the pathways that can improve the immunogenicity of inactivated vaccines is to increase the dose of influenza antigens contained in the vaccine. Studies have demonstrated that increasing the dose of the influenza virus hemagglutinin for each of the commonly encountered viral strains beyond the conventional dose of 15 microgram for each strain is associated with dose-dependent increase in serum antibody titers.

Influenza TIV is commercially available in two different strengths, Fluzone as well as Fluzone High-Dose, and it is valuable because of variable immunogenic potency of different strengths. Fluzone is approved for use in persons 6 months of age and older. High-dose Fluzone is approved for use in persons 65 years of age and older.

The purpose of this exploratory study is to assess the safety, tolerability, and immunogenicity of these two commercially available different strengths of TIV in solid organ transplant recipients (kidney, heart and lung) in the period after 30 days after transplant procedure. We will evaluate the safety, tolerability (reactogenicity) and immunogenicity of two different strengths of commercially available TIV in a single center, cluster randomization, investigator blinded, study by enrolling patients in the post-transplant clinic at Inova Fairfax Hospital from: August 1, 2013 - March 31, 2014; and August 1, 2014 to March 31, 2015.

Study protocol will remain active till December 31, 2016. All bio-specimens will be stored till December 31, 2016.

Study Timeline

• Study First Submitted: 2013-03-04
• Study First Submitted QC: 2013-03-07
• Study First Posted: 2013-03-11
• Study Start: 2013-10
• Primary Completion: 2016-12
• Study Completion: 2016-12
• Results First Submitted: 2021-04-28
• Status Verified: 2022-07
• Results First Submitted QC: 2022-07-20
• Last Update Submitted: 2022-07-20
• Results First Posted: 2022-07-22
• Last Update Posted: 2022-07-22

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 62

Inclusion Criteria

1. All adults age ≥18 years of age following solid organ transplants (kidney, heart and lung) of all races and gender unless as specified in the exclusion criteria.
2. At least 30 days after organ transplantation of kidney, heart, or lung.
3. In good health as determined by a) medical history, b) physical examinations, c) clinical judgment of the investigator team.
4. Informed consent will be obtained from all the subjects before enrollment into the study, after the nature of the study has been fully explained to the satisfaction of the participant.
5. Non-English speaking persons will be included ONLY if consent can be obtained with the help of the translator or interpreter.

Exclusion Criteria

1. Less than 30 days after transplantation procedure.
2. Post operative complications of any type.
3. Transplant organ dysfunction and/or under evaluation for possible infection.
4. Recent acute transplant rejection and treatment for rejection for the past 30 days.
5. Receiving another investigational drug or biologic for transplant.
6. Previous history of allergic reaction to influenza vaccine, chicken egg or other unknown allergic reactions to flu vaccine or other vaccines.
7. Acute ongoing respiratory illness.
8. Bleeding diathesis or on anticoagulation therapy.
9. Major surgery (pre-arranged) planned during the study period.
10. Any condition that may preclude the participant from completion of study related activities; such as planned travel, or out of the state of residence and not able to return for follow-up visits or relocation of residence.
11. Females of reproductive age unless proven to be urine HCG negative at the time of participation.
12. Recent opportunistic infection, such as CMV, EBV, BK viral reactivation, or any other documented or laboratory confirmed opportunistic infection or on treatment for confirmed infection.
13. Vulnerable subjects such as aged less than 18 years, pregnant women, nursing home residents or other institutionalized persons, students, employees, prisoners, and persons who may not be able to make independent decisions or is considered to have a cognitive impairment, or non-English speaking in the absence of a reliable interpreter or translator.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Flu Vaccine	influenza trivalent inactive vaccine	influenza trivalent inactive vaccine IM injection one time administration
High Dose Flu Vaccine	influenza trivalent inactive vaccine high dose	influenza trivalent inactive vaccine high dose. IM (intramuscular) injection one time administration

Primary Outcome Measures

Name	Time	Method
Number of Patients With Local Site Reactions	Day 1 and weeks 1, 4, and 12	Evaluation of local and systemic reactions, use of analgesics or antipyretics.
Measurement of Strain-specific Hemagglutination Inhibition (HI) Antibody Titers	Week 1, 4, and 12	Number of patients and percentage of subjects achieving hemagglutination inhibition (HI) titer≥40

Secondary Outcome Measures

Name	Time	Method
Number and Percentage of Subjects in Each Group Achieving Seroconversion for Each Strain	Week 4 and Week 12	Number and percentage of subjects in each group achieving seroconversion (at least 4-fold increase in titers from baseline) for each any strain at weeks 4 and 12
All Cause ED Visits/Unscheduled Clinic Visits	day 1 - 3 months	All-cause outpatient/Emergency department visits during study follow-up (other than pre-specified post transplant follow-up visits).

Trial Locations

Locations (1)

Inova Fairfax Hospital; 🇺🇸 Falls Church, Virginia, United States