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Pneumococcal Vaccination of Crohn Patients (PneuVAC)

Primary Purpose

Crohns Disease

Status
Completed
Phase
Phase 4
Locations
Denmark
Study Type
Interventional
Intervention
Prevenar 13
Pneumovax
Sponsored by
Statens Serum Institut
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Crohns Disease focused on measuring antibodies

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Crohn's disease, receive immunosuppressive treatment or no treatment

Exclusion Criteria:

  • <18 years of age,
  • pregnant,
  • anemia,
  • previously pneumococcus vaccination

Sites / Locations

  • Statens Serum Institut

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

Crohn's patients treated with Azathioprine

Crohn's patients treated with Azathioprine and TNFa inhibitors

Crohn's disease patients without treatment

Arm Description

Vaccination with PPV23 or Vaccination with PCV 13

Vaccination with PPV23 or Vaccination with PCV 13

Vaccination with PPV23 or Vaccination with PCV 13

Outcomes

Primary Outcome Measures

Change in antibody titers
The primary outcome is to detect a difference in antibody change between the two vaccines as a consequence of the vaccination

Secondary Outcome Measures

Change in antibody titers as a function of Crohns disease treatment
The secondary outcome is to detect a difference in antibody change between the two vaccines as a function of the treatment for Crohns disease.

Full Information

First Posted
September 9, 2013
Last Updated
February 6, 2015
Sponsor
Statens Serum Institut
Collaborators
Hvidovre University Hospital, Herlev Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01947010
Brief Title
Pneumococcal Vaccination of Crohn Patients
Acronym
PneuVAC
Official Title
Pneumococcal Vaccination of Crohn Patients - A Randomized, Non-blinded Phase 4 Clinical Trial With the Purpose of Investigating the Immune Response Against Two Different Pneumococcal Vaccines in Patients With Crohn's Disease
Study Type
Interventional

2. Study Status

Record Verification Date
February 2015
Overall Recruitment Status
Completed
Study Start Date
July 2013 (undefined)
Primary Completion Date
August 2014 (Actual)
Study Completion Date
August 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Statens Serum Institut
Collaborators
Hvidovre University Hospital, Herlev Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Inflammatory bowel disease (IBD) are at increased risk of infections. This increased susceptibility to infections is due to the disease itself, but also be-cause many patients with autoimmune conditions are treated with immuno-suppressive drugs, such as azathioprine and or TNF-a inhibitors. Streptococcus pneumoniae (pneumococcus) is a cause of worldwide morbidity and mortality and one of the most common cause of bacterial meningitis in adults. Infection with pneumococcus can be prevented with vaccination. Two pneumococcal vaccine are used in Denmark, the 23 valent polysaccharide-based vaccine (23PPV) and the 13 valent of conjugate pneumococcal vaccines (PCV13). In this study the investigators wish to study the effect of pneumococcal vaccination with either PPV23 or PCV13 in IBD patients treated with either TNF-a inhibitors, azathioprine or untreated.
Detailed Description
Patients with autoimmune diseases like inflammatory bowel disease (IBD) and rheumatoid arthritis (RA) are at increased risk of infections. This increased susceptibility to infections is due to the disease itself, but also be-cause many patients with autoimmune conditions are treated with immuno-suppressive drugs. Different drugs are well-known suppressors of the immune system: Prednisolone, Azathioprine, Methotrexate (MTX), TNF-a inhibitors, and the newer biological agents such as, e.g., Rituximab (RTX), which is a drug used in the treatment of RA patients often in combination with MTX. The extent of immunosuppression induced by these therapeutic agents seems to depend, to some extent, on pharmacological dose/response relationships and on the combination of drugs, but individual variability plays a major role as well. Prophylactic measures such as vaccination, quick upstart of antibiotics in case of fever and general information to patients about how to handle fever etc. are important in order to prevent as many cases of serious infections as possible among patients in immunosuppressive treatment. Streptococcus pneumoniae is a cause of worldwide morbidity and mortality. Pneumococcal vaccines have been available since the early 1980's. The vaccine which has been licensed for immunization of children >2 years and adults is a polysaccharide-based vaccine (23PPV) consisting of capsule parts of the 23 most frequent serotypes of pneumococci. This vaccine elicits in normal immunocompetent persons a high antibody response, which lasts for approximately 10 years. Because the 23PPV is a polysaccharide-based vaccine, it induces a T-cell independent response with no memory and there-fore with no possibility of boosting. In 2001, the first generation of conjugate pneumococcal vaccines (PCV7) was licensed. In the PCV's, the capsule material from the pneumococci has been conjugated to a protein, which means that the vaccines can elicit a T-cell dependent immune response even in infants giving memory response and booster possibility. This vaccine has been licensed for use in children from 0-5 years, but studies suggest that PCV immunization might be useful in other groups of people as well etc. immunodeficient children and adults (especially now where the second-generation vaccines PCV10, PCV13 have been licensed covering more pneumococcal serotypes). Some studies have shown that patients treated with immunosuppressive drugs cannot mount a sufficient antibody response upon vaccination whereas other studies suggest that these patient groups do respond to conventional vaccination. It is recommended in the Danish guidelines for pneumococcal vaccination, that elderly patients with chronic diseases and patients with a decreased immune system are vaccinated against pneumococcal diseases. Accordingly, patients with Crohn's disease treated with TNF-a inhibitors are recommended pneumococcal vaccination. In this study, the investigators aim to carry out an investigation of the response to pneumococcal vaccination in persons with Crohn's disease treated with TNF-a inhibitors and/or azathioprine, in order to determine if there is a place for the usage of conjugate vaccination in these patient groups.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Crohns Disease
Keywords
antibodies

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
151 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Crohn's patients treated with Azathioprine
Arm Type
Active Comparator
Arm Description
Vaccination with PPV23 or Vaccination with PCV 13
Arm Title
Crohn's patients treated with Azathioprine and TNFa inhibitors
Arm Type
Active Comparator
Arm Description
Vaccination with PPV23 or Vaccination with PCV 13
Arm Title
Crohn's disease patients without treatment
Arm Type
Active Comparator
Arm Description
Vaccination with PPV23 or Vaccination with PCV 13
Intervention Type
Biological
Intervention Name(s)
Prevenar 13
Intervention Type
Biological
Intervention Name(s)
Pneumovax
Primary Outcome Measure Information:
Title
Change in antibody titers
Description
The primary outcome is to detect a difference in antibody change between the two vaccines as a consequence of the vaccination
Time Frame
Day 0, 4 weeks post vaccination, 1 year post vaccination
Secondary Outcome Measure Information:
Title
Change in antibody titers as a function of Crohns disease treatment
Description
The secondary outcome is to detect a difference in antibody change between the two vaccines as a function of the treatment for Crohns disease.
Time Frame
Day 0, 4 weeks post vaccination, 1 year post vaccination

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Crohn's disease, receive immunosuppressive treatment or no treatment Exclusion Criteria: <18 years of age, pregnant, anemia, previously pneumococcus vaccination
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andreas M Petersen, MD
Organizational Affiliation
Hvidovre University Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ole Ø Thomsen, MD
Organizational Affiliation
Herlev Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Statens Serum Institut
City
Copenhagen
ZIP/Postal Code
2300
Country
Denmark

12. IPD Sharing Statement

Citations:
PubMed Identifier
31290715
Citation
Kantso B, Halkjaer SI, Ostergaard Thomsen O, Belard E, Gottschalck IB, Jorgensen CS, Krogfelt KA, Slotved HC, Ingels H, Petersen AM. Persistence of antibodies to pneumococcal conjugate vaccine compared to polysaccharide vaccine in patients with Crohn's disease - one year follow up. Infect Dis (Lond). 2019 Sep;51(9):651-658. doi: 10.1080/23744235.2019.1638519. Epub 2019 Jul 10.
Results Reference
derived
PubMed Identifier
26275480
Citation
Kantso B, Halkjaer SI, Thomsen OO, Belard E, Gottschalck IB, Jorgensen CS, Krogfelt KA, Slotved HC, Ingels H, Petersen AM. Immunosuppressive drugs impairs antibody response of the polysaccharide and conjugated pneumococcal vaccines in patients with Crohn's disease. Vaccine. 2015 Oct 5;33(41):5464-5469. doi: 10.1016/j.vaccine.2015.08.011. Epub 2015 Aug 12.
Results Reference
derived

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Pneumococcal Vaccination of Crohn Patients

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