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HUmira in Psoriatic Arthritis (HUPSA)

Primary Purpose

Psoriatic Arthritis

Status
Completed
Phase
Phase 4
Locations
Denmark
Study Type
Interventional
Intervention
Adalimumab
Sponsored by
Glostrup University Hospital, Copenhagen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Psoriatic Arthritis

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Subject Population: patients with active PsA, fulfilling the following major criteria:

  1. Diagnosis of PsA according to Moll and Wright criteria (Moll and Wright,
  2. Clinical active disease, defined as >2 (of 76) swollen joints and > 2 (of 78) tender joints
  3. Involvement of the hands (Clinical swelling of 1 or more finger joint and/or 1 or more 1 sausage finger)
  4. Clinical indication for anti-TNF alpha therapy, according to treating physician
  5. Among other issues: Age >18 years; adequate birth control; no contraindications for anti-TNF alpha-therapy, no previous anti-TNF alpha-therapy, no other significant dermatological disorders than psoriasis.

Sites / Locations

  • Copenhagen University Hospital, Glostrup

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Adalimumab

Arm Description

Responders at week 24 continue treatment with adalimumab. Non-responders at week 24 stops treatment with adalimumab.

Outcomes

Primary Outcome Measures

Modified Psoriatic Arthritis Response criteria (PsARC)

Secondary Outcome Measures

Full Information

First Posted
June 16, 2011
Last Updated
November 3, 2011
Sponsor
Glostrup University Hospital, Copenhagen
Collaborators
University Hospital, Gentofte, Copenhagen, Copenhagen University Hospital at Herlev, Copenhagen University Hospital, Hvidovre
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1. Study Identification

Unique Protocol Identification Number
NCT01465438
Brief Title
HUmira in Psoriatic Arthritis
Acronym
HUPSA
Official Title
Can New Imaging- and Biomarkers Improve the Assessment of Disease Activity and Progression and Predict Therapeutic Outcome in Psoriatic Arthritis Patients Receiving Adalimumab?
Study Type
Interventional

2. Study Status

Record Verification Date
February 2011
Overall Recruitment Status
Completed
Study Start Date
November 2006 (undefined)
Primary Completion Date
June 2011 (Actual)
Study Completion Date
June 2011 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Glostrup University Hospital, Copenhagen
Collaborators
University Hospital, Gentofte, Copenhagen, Copenhagen University Hospital at Herlev, Copenhagen University Hospital, Hvidovre

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Psoriatic arthritis (PsA) is an inflammatory arthritis associated with psoriasis, which has a estimated prevalence of 0.3 - 1 %. The clinical course varies, but PsA is often a progressive, erosive arthritis causing severe disability and increased mortality. The biologic treatment infliximab and etanercept have recently been introduced for treatment of PsA and psoriasis, and current data indicate a higher efficacy than with previously available therapies. No clinical trials on adalimumab in PsA are yet published (2005), but preliminary data are encouraging. The improved treatment options have increased the need for sensitive methods for diagnosis, monitoring and prognostication of PsA, so that the efficient therapies can be initiated at the optimal time point and monitored optimally. Ultrasonography (US) and magnetic resonance imaging (MRI) and a number of biomarkers are promising, but not yet sufficiently studied, methods for this. The hypothesis is that adalimumab will be an effective treatment option for PsA. Novel imaging- and biomarkers can provide additional information, compared to clinical measures and radiography, concerning activity, destructive progression and prediction of therapeutic response in PsA patients receiving adalimumab. The perspective is a potential improvement in diagnosis, monitoring and prognostication of patients with PsA.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Psoriatic Arthritis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
42 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Adalimumab
Arm Type
Experimental
Arm Description
Responders at week 24 continue treatment with adalimumab. Non-responders at week 24 stops treatment with adalimumab.
Intervention Type
Drug
Intervention Name(s)
Adalimumab
Other Intervention Name(s)
Humira
Intervention Description
Adalimumab 40 mg every other week
Primary Outcome Measure Information:
Title
Modified Psoriatic Arthritis Response criteria (PsARC)
Time Frame
24 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subject Population: patients with active PsA, fulfilling the following major criteria: Diagnosis of PsA according to Moll and Wright criteria (Moll and Wright, Clinical active disease, defined as >2 (of 76) swollen joints and > 2 (of 78) tender joints Involvement of the hands (Clinical swelling of 1 or more finger joint and/or 1 or more 1 sausage finger) Clinical indication for anti-TNF alpha therapy, according to treating physician Among other issues: Age >18 years; adequate birth control; no contraindications for anti-TNF alpha-therapy, no previous anti-TNF alpha-therapy, no other significant dermatological disorders than psoriasis.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Charlotte Wiell, MD, PhD
Organizational Affiliation
University Hospital, Gentofte, Copenhagen
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Inge Juul Sørensen, MD, PhD
Organizational Affiliation
Copenhagen University Hospital, Hvidovre
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Michael Sejer Hansen, MD, PhD
Organizational Affiliation
Copenhagen University Hospital at Herlev
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ole Rintek Madsen, MD, PhD
Organizational Affiliation
University Hospital, Gentofte, Copenhagen
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ole Slot, MD
Organizational Affiliation
Glostrup University Hospital, Copenhagen
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Susanne J Pedersen, MD
Organizational Affiliation
Gentofte University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Copenhagen University Hospital, Glostrup
City
Glostrup
State/Province
Copenhagen
ZIP/Postal Code
2600
Country
Denmark

12. IPD Sharing Statement

Citations:
PubMed Identifier
24369412
Citation
Poggenborg RP, Wiell C, Boyesen P, Boonen A, Bird P, Pedersen SJ, Sorensen IJ, Madsen OR, Slot O, Moller JM, Hasselquist M, Kubassova O, Ostergaard M. No overall damage progression despite persistent inflammation in adalimumab-treated psoriatic arthritis patients: results from an investigator-initiated 48-week comparative magnetic resonance imaging, computed tomography and radiography trial. Rheumatology (Oxford). 2014 Apr;53(4):746-56. doi: 10.1093/rheumatology/ket426. Epub 2013 Dec 24.
Results Reference
derived

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HUmira in Psoriatic Arthritis

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