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Adalimumab in Alleviating Inflammation in Patients With Axial Spondyloarthritis (PETSPA)

Primary Purpose

Ankylosing Spondyloarthritis

Status
Unknown status
Phase
Phase 4
Locations
Finland
Study Type
Interventional
Intervention
Adalimumab
PET/CT imaging
Sponsored by
University of Helsinki
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ankylosing Spondyloarthritis

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Axial spondyloarthritis (ASAS criteria) and radiologic sacroiliitis as detected either by MRI or X-ray.

Exclusion Criteria:

  • Psoriasis or psoriasis arthropathy
  • Inflammatory bowel disease
  • Unwillingness to participate in the study with additional imaging protocols
  • Expected life-span less than <1 year
  • Diabetes (to improve the PET imaging quality)
  • Probable noncompliance
  • Pregnancy
  • Age <18 years or >75 years
  • Contraindication for adalimumab
  • Methotrexate used within the previous 6 months
  • A biologic medicine used within the previous 6 months

Sites / Locations

  • Helsinki University Central HospitalRecruiting
  • Päijät-Häme Central HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

DMARD-naive

Post-sulfasalazine

Arm Description

Sulfasalazine will be given as the initial therapy.

Sulfasalazine contraindicated or not efficient, adalimumab will be given as the initial therapy.

Outcomes

Primary Outcome Measures

PET signals within groups
Decrease in PET signal levels both in major CV tissues (mean TBR in the whole aorta) and musculoskeletal tissues (lumbar spine and articular enthesitis as well as arthritis) after antirheumatic treatment. Thus the variables of most interest reflect intraindividual changes.

Secondary Outcome Measures

PET signals between groups
Comparison of the pre-treatment PET signals between the three groups: those with axial spondyloarthritis, historical healthy controls and the patients with coronary heart disease.

Full Information

First Posted
December 16, 2015
Last Updated
February 22, 2017
Sponsor
University of Helsinki
Collaborators
AbbVie
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1. Study Identification

Unique Protocol Identification Number
NCT02634541
Brief Title
Adalimumab in Alleviating Inflammation in Patients With Axial Spondyloarthritis
Acronym
PETSPA
Official Title
The Efficacy of Adalimumab and Conventional Antirheumatic Drugs in Alleviating Axial and Aortic Inflammation Detected in PET/CT in Patients With Axial Spondyloarthritis
Study Type
Interventional

2. Study Status

Record Verification Date
February 2017
Overall Recruitment Status
Unknown status
Study Start Date
January 2016 (Actual)
Primary Completion Date
December 2017 (Anticipated)
Study Completion Date
December 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Helsinki
Collaborators
AbbVie

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Axial spondyloarthritis is an inflammatory rheumatic disease mainly affecting joints in the spine and the sacroiliac joints. Inflammatory pathways are likely the central link from axial spondyloarthritis to the known increased risk of atherosclerotic morbidity. Positron emission tomography (PET) is the most sensitive method to detect inflammatory foci in clinical practice. A few small studies have demonstrated that PET imaging together with computed tomography (PET/CT) detects inflamed tissues in relevant patient groups. One study suggested that antirheumatic treatment diminishes the inflammation detected in PET/CT. No study so far has disclosed whether aortic inflammation is present in patients with spondyloarthritis, and whether the inflammation would wane with efficient antirheumatic treatment. The current study is aimed to grade the articular and aortic inflammatory signals in the PET/CT imaging before and after antirheumatic treatment of clinically active axial spondyloarthritis. Sixty patients aged 18-75 years with axial spondyloarthritis and radiologic sacroiliitis as detected either by MRI or X-ray will be recruited. Twenty of those are DMARD-naive, and 40 patients have axial spondyloarthritis resistant to sulfasalazine or other conventional antirheumatic drug. In addition, approximately 30 patients without spondyloarthritis but with stable coronary heart disease and approximately 20 healthy controls will be taken as historical controls. All the axial spondyloarthritis patients are PET/CT scanned after inclusion in the study. The DMARD-naive patients (n=20) are started sulfasalazine-based regimen for 12 weeks, which is the time point for a second PET scan for this subgroup. Adalimumab will be commenced for those without remission at 12 weeks. After another 16 weeks, those with adalimumab will be scanned with PET/CT for the third time. The subgroup with active disease in spite of prior conventional treatment (n=40) is also scanned with PET/CT right after the enrolment and after 16-week treatment with adalimumab. The first 15 patients form a pilot group, which is used to check the validity of the power calculation. The project will give essential new information on PET-detectable inflammation in the patients with axial spondyloarthritis. The results will be published in international publication series. The publications will form the basis for a doctoral thesis. Funding for the project comes from Abbvie Ltd.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ankylosing Spondyloarthritis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
DMARD-naive
Arm Type
Active Comparator
Arm Description
Sulfasalazine will be given as the initial therapy.
Arm Title
Post-sulfasalazine
Arm Type
Experimental
Arm Description
Sulfasalazine contraindicated or not efficient, adalimumab will be given as the initial therapy.
Intervention Type
Drug
Intervention Name(s)
Adalimumab
Intervention Description
Biologic drug
Intervention Type
Other
Intervention Name(s)
PET/CT imaging
Intervention Description
PET/CT imaging
Primary Outcome Measure Information:
Title
PET signals within groups
Description
Decrease in PET signal levels both in major CV tissues (mean TBR in the whole aorta) and musculoskeletal tissues (lumbar spine and articular enthesitis as well as arthritis) after antirheumatic treatment. Thus the variables of most interest reflect intraindividual changes.
Time Frame
16 weeks
Secondary Outcome Measure Information:
Title
PET signals between groups
Description
Comparison of the pre-treatment PET signals between the three groups: those with axial spondyloarthritis, historical healthy controls and the patients with coronary heart disease.
Time Frame
16 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Axial spondyloarthritis (ASAS criteria) and radiologic sacroiliitis as detected either by MRI or X-ray. Exclusion Criteria: Psoriasis or psoriasis arthropathy Inflammatory bowel disease Unwillingness to participate in the study with additional imaging protocols Expected life-span less than <1 year Diabetes (to improve the PET imaging quality) Probable noncompliance Pregnancy Age <18 years or >75 years Contraindication for adalimumab Methotrexate used within the previous 6 months A biologic medicine used within the previous 6 months
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Tuomo Nieminen, PhD, MD
Phone
+358 50 910 5150
Email
tuomo.vm.nieminen@helsinki.fi
First Name & Middle Initial & Last Name or Official Title & Degree
Anne Kerola, BMS
Phone
+358 50 360 0550
Email
anne.kerola@helsinki.fi
Facility Information:
Facility Name
Helsinki University Central Hospital
City
Helsinki
Country
Finland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tuomo Nieminen
Email
tuomo.vm.nieminen@helsinki.fi
Facility Name
Päijät-Häme Central Hospital
City
Lahti
Country
Finland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anne Kerola
Email
anne.kerola@helsinki.fi

12. IPD Sharing Statement

Plan to Share IPD
No

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Adalimumab in Alleviating Inflammation in Patients With Axial Spondyloarthritis

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