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Infliximab IBD Influenza Vaccine Study

Primary Purpose

Inflammatory Bowel Disease

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Influenza vaccination
Sponsored by
University of Calgary
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Inflammatory Bowel Disease focused on measuring Influenza vaccine, Immune response, Remicade (infliximab), Inflammatory bowel disease

Eligibility Criteria

9 Years - 60 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosis of IBD established by accepted criteria
  • On maintenance infliximab administered every 6 to 8 weeks (already received at least 6 weeks of infliximab)
  • Between ages 9 and 60 years

Exclusion Criteria:

  1. Pregnancy
  2. Hypersensitivity reaction to previous dose of influenza vaccine
  3. Known hypersensitivity to eggs or chicken or other components of influenza vaccine

Sites / Locations

  • University of Calgary

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Influenza vaccination Timing #1

Influenza vaccination Timing #2

Arm Description

Influenza vaccination administered on the same day as infliximab administration (Day 0 to 4).

Influenza vaccination administered at the mid-point between infliximab infusions (Day 21 to 28)

Outcomes

Primary Outcome Measures

Serologic protection
To compare the proportion of IBD patients on maintenance infliximab who mount serologic protection to each component of the influenza vaccination between patients vaccinated on day of infliximab infusion (Day 0 to 4) and patients vaccinated at the mid-point between infliximab infusions (Day 21 to 28). Serologic protection will be defined by a hemagglutination-inhibition titer ≥ 1:40.

Secondary Outcome Measures

Immunogenic response
To compare the proportion of IBD patients on maintenance infliximab who mount an immunogenic response to each component of the influenza vaccination between patients vaccinated on day of infliximab infusion (Day 0 to 4) and patients vaccinated at the mid-point between infliximab infusions (Day 21 to 28). Immunogenicity will be defined as a fourfold or greater differences in titer between pre and post-vaccination sera.

Full Information

First Posted
August 8, 2012
Last Updated
May 5, 2016
Sponsor
University of Calgary
Collaborators
Janssen Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT01666535
Brief Title
Infliximab IBD Influenza Vaccine Study
Official Title
Effect of Influenza Vaccination Timing on Immune Response in Patients With Inflammatory Bowel Disease on Infliximab Therapy: A Randomized Equivalence Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2016
Overall Recruitment Status
Completed
Study Start Date
September 2012 (undefined)
Primary Completion Date
March 2013 (Actual)
Study Completion Date
August 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Calgary
Collaborators
Janssen Inc.

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The investigators will compare the immunogenicity of influenza vaccine in adults and children with inflammatory bowel disease by timing of vaccine in relation to maintenance infliximab dosing. The primary objective is to compare the proportion of IBD patients on maintenance infliximab who mount serologic protection to each component of the influenza vaccination between patients vaccinated on day of infliximab infusion (Day 0 to 4) and patients vaccinated at the mid-point between infliximab infusions (Day 21 to 28). Serologic protection will be defined by a hemagglutination-inhibition titer ≥ 1:40. The secondary objective is to compare the proportion of IBD patients who mount an immunogenic response (≥ 4-fold increase from pre to post-vaccination titer) to each component of the influenza vaccination between patients vaccinated on day of infliximab infusion and those vaccinated at the mid-point.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Inflammatory Bowel Disease
Keywords
Influenza vaccine, Immune response, Remicade (infliximab), Inflammatory bowel disease

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
137 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Influenza vaccination Timing #1
Arm Type
Other
Arm Description
Influenza vaccination administered on the same day as infliximab administration (Day 0 to 4).
Arm Title
Influenza vaccination Timing #2
Arm Type
Other
Arm Description
Influenza vaccination administered at the mid-point between infliximab infusions (Day 21 to 28)
Intervention Type
Biological
Intervention Name(s)
Influenza vaccination
Primary Outcome Measure Information:
Title
Serologic protection
Description
To compare the proportion of IBD patients on maintenance infliximab who mount serologic protection to each component of the influenza vaccination between patients vaccinated on day of infliximab infusion (Day 0 to 4) and patients vaccinated at the mid-point between infliximab infusions (Day 21 to 28). Serologic protection will be defined by a hemagglutination-inhibition titer ≥ 1:40.
Time Frame
28 days ± 3 days after influenza vaccination
Secondary Outcome Measure Information:
Title
Immunogenic response
Description
To compare the proportion of IBD patients on maintenance infliximab who mount an immunogenic response to each component of the influenza vaccination between patients vaccinated on day of infliximab infusion (Day 0 to 4) and patients vaccinated at the mid-point between infliximab infusions (Day 21 to 28). Immunogenicity will be defined as a fourfold or greater differences in titer between pre and post-vaccination sera.
Time Frame
28 days ± 3 days after influenza vaccination
Other Pre-specified Outcome Measures:
Title
Number of participants with serious adverse events
Description
To evaluate the number of participants with early serious adverse reactions (≤ 3 days post-vaccination)
Time Frame
3 days post vaccination
Title
Change in disease activity from baseline
Description
To evaluate the change in disease activity score from baseline using the validated instruments of the Pediatric Ulcerative Colitis Activity Index for participants with Ulcerative Coltiis and the Harvey Bradshaw Index for participants with Crohn's Disease
Time Frame
Four week post-vaccination

10. Eligibility

Sex
All
Minimum Age & Unit of Time
9 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of IBD established by accepted criteria On maintenance infliximab administered every 6 to 8 weeks (already received at least 6 weeks of infliximab) Between ages 9 and 60 years Exclusion Criteria: Pregnancy Hypersensitivity reaction to previous dose of influenza vaccine Known hypersensitivity to eggs or chicken or other components of influenza vaccine
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jennifer deBruyn, MD
Organizational Affiliation
University of Calgary
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Calgary
City
Calgary
State/Province
Alberta
ZIP/Postal Code
T3B 6A8
Country
Canada

12. IPD Sharing Statement

Learn more about this trial

Infliximab IBD Influenza Vaccine Study

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