Ankylosing spondylitis (AS) is a chronic inflammatory disease that involves the sacroiliac joints, axial skeleton, entheses and peripheral joints. Current therapy for AS is mainly NSAIDs and physiotherapy which are oft insufficient. Treatment with the TNF-alpha blocking agent infliximab was shown to have definite clinical efficacy in patients with active AS on a short- and a long-term-basis over 2 years. We want to show that treatment with infliximab on a long-term basis over 4 years is safe and efficient and can prevent radiographic progression over a long period of time. Further we want to learn about the outcome after discontinuation of anti-TNF-alpha therapy.

Condition	Intervention
Ankylosing Spondylitis	Drug: infliximab

Further study details as provided by Rheumazentrum Ruhrgebiet:

Primary Outcomes: Degree of structural damage (radiographic progression)after 4 years of infliximab therapy (2 years of ASSERT trial plus 2 years of EASIC trial)
Secondary Outcomes: Proportion of patients which have received anti-TNF-alpha therapy as standard care after the end of ASSERT; Description of the various treatment regimens after the end of ASSERT of the participating AS patients in various countries; Degree of spinal inflammation analyzed by MRI after discontinuation of infliximab and 4-8 weeks and 2 years after re-treatment; Long-term efficacy of infliximab over 4 years of therapy measured by the ASAS response criteria; Efficacy and safety of a new start of infliximab therapy after discontinuation for several months after 2 years of continuous treatment; Long-term effects on QoL; Long-term effects on health resource utilisation and productivity in paid and unpaid work
Expected Total Enrollment:  149

Ankylosing spondylitis (AS) is a chronic inflammatory disease of unknown etiology that involves the sacroiliac joints, axial skeleton, entheses and peripheral joints. Chronic inflammation of entheses leads to new bone formation, syndesmophytes and ankylosis of joints, primarily in the axial skeleton. This leads to a dramatic loss of range of motion and to disability. The disease may also have nonskeletal manifestations including uveitis, carditis, pulmonary fibrosis and cardiac conduction abnormalities.

Current therapy for AS is mainly with NSAIDs and physiotherapy which are often insufficient. Clinical outcome with conventional therapies has not been good, with 50-70% of patients progressing to fusion of the spine by 10 to 15 years. Treatment with the TNF-alpha blocking agent infliximab was shown to have definite clinical efficacy in patients with active ankylosing spondylitis on a short- and a long-term basis over 2 years.

There is limited data available on the efficacy and safety of long-term anti-TNF therapy for 3 and more years, the outcome after discontinuation of anti-TNF therapy and the effect of anti-TNF therapy on radiographic progression over a long period of time.

The ASSERT trial was a 2 year international randomized placebo controlled trial to evaluate the efficacy and safety ot treatment with infliximab in patients with active and severe AS. The EASIC trial is initiated to follow the European participants of the ASSERT trial for at least an additional 2 years of treatment combined with systematic data collection.

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

• All patients in Europe who have completed visit "week 96" of ASSERT (last infusion of infliximab)
• Capacity to understand and sign an informed consent form
• Capacity to read and understand subject assessment forms
• Using adequate birth control measures for the duration of the study and for 6 months after receiving the last infusion, if the patient is of childbearing potential
• Serum creatinine < 1,4 mg/dl
• Hemoglobin > 9,0 mg /dl for males and > 8,5 mg/dl for females
• Serum transaminase levels within 3 times the upper limit of normal range

Exclusion Criteria:

• Have used systemic prednisolone > 20 mg during the 2 weeks prior to screening
• Have used cytotoxic drugs after the end of ASSERT including chlorambucil, cyclophosphamide and alkylating agents
• Have received any previous treatment with etanercept or any other anti-TNF agent (other than infliximab) after the end of the ASSERT trial
• General medical exclusion criteria
• Use of any investigational drug within 30 days prio to screening
• Concomitant diagnosis or history of congestive heart failure
• History of latent or active tuberculosis
• Signs or symptoms suggestive of active tuberculosis
• Recent close contact with a person with active tuberculosis

Please refer to this study by ClinicalTrials.gov identifier  NCT00237419

Jürgen Braun, Prof. Dr.      +49 (0) 2325 592131    j.braun@rheumazentrum-ruhrgebiet.de
Frank Heldmann, Dr. med.      + 49 (0) 2325 592138    heldmann@rheumazentrum-ruhrgebiet.de

Belgium
      University Hospital Leuven, Leuven,  3000,  Belgium
      Limburg University Centre, Diepenbeek,  Belgium
      Erasme University Hospital, Brussels,  Belgium
      Universitair Ziekenhuis, Afdeling Rheumatologie, Gent,  9000,  Belgium
Finland
      University Central Hospital, Division of Rheumatology, Helsinki,  00029HYKS,  Finland
France
      Groupe Hopitalier Cochin, Paris,  France
      Universitat R. Descartes, Hopital Cochin, Paris,  France
Germany
      Charite Mitte, Berlin,  10117,  Germany
      Charite Klinikum Steglitz, Berlin,  12200,  Germany
      Ludwigs-Maximilian-Universität, München,  80336,  Germany
      Rheumazentrum Ruhrgebiet, Herne,  44652,  Germany
Netherlands
      University Hospital Maastricht, Maastricht,  6202 AZ,  Netherlands
      Academic Ziekenhuis, Amsterdam,  1007MB,  Netherlands
United Kingdom
      University of Leeds, Leeds,  LS2 9N2,  United Kingdom
      University of Cambridge/ Clin Med, Cambridge,  CB2 QQ,  United Kingdom

Study chairs or principal investigators

Jürgen Braun, Prof. Dr.,  Principal Investigator,  Rheumazentrum Ruhrgebiet   

Study ID Numbers:  EASIC 30505
Last Updated:  December 8, 2005
Record first received:  October 10, 2005
ClinicalTrials.gov Identifier:  NCT00237419
Health Authority: Germany: Paul-Ehrlich-Institut
ClinicalTrials.gov processed this record on 2006-01-10