A Study of Infliximab (Remicade) in Patients With Ankylosing Spondylitis.
Primary Purpose
Ankylosing Spondylitis
Status
Completed
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
infliximab
Sponsored by
About this trial
This is an interventional treatment trial for Ankylosing Spondylitis focused on measuring Ankylosing Spondylitis, infusion
Eligibility Criteria
Inclusion Criteria: Have had a diagnosis of definite Akylosing Spondylitis for at least 3 months prior to screening Have active disease with spinal pain receiving or intolerant to standard anti-inflammatory agents Exclusion Criteria: Have Rheumatoid Arthritis, systemic lupus erythematosus, or other inflammatory rheumatic disease Have a documented history of fibromyalgia Have total ankylosis
Sites / Locations
Outcomes
Primary Outcome Measures
The primary endpoint of this study was the proportion of subjects who achieved an ASAS 20 response at week 24.
Secondary Outcome Measures
The change from baseline in BASFI at week 24, the proportion of subjects who achieved an AS major clinical response at week 24, and the change from baseline in the physical component summary score of the SF-36 at week 24
Full Information
NCT ID
NCT00207701
First Posted
September 13, 2005
Last Updated
May 16, 2011
Sponsor
Centocor, Inc.
Collaborators
Centocor BV
1. Study Identification
Unique Protocol Identification Number
NCT00207701
Brief Title
A Study of Infliximab (Remicade) in Patients With Ankylosing Spondylitis.
Official Title
A Randomized, Double-blind Trial of the Efficacy of REMICADE (Infliximab) Compared With Placebo in Subjects With Ankylosing Spondylitis Receiving Standard Anti-inflammatory Drug Therapy
Study Type
Interventional
2. Study Status
Record Verification Date
August 2010
Overall Recruitment Status
Completed
Study Start Date
September 2002 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
February 2005 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Centocor, Inc.
Collaborators
Centocor BV
4. Oversight
5. Study Description
Brief Summary
A study of the safety and efficacy of Infliximab (Remicade) versus placebo in subjects with Ankylosing Spondylitis
Detailed Description
This is a clinical research study that will determine if there is a reduction in the signs and symptoms (such as back pain and stiffness) of patients with ankylosing spondylitis with infliximab therapy. This study will also study the safety of infliximab in patients with ankylosing spondylitis. The effect of infliximab on physical function, damage to joints and the quality of life in patients with ankylosing spondylitis will also be studied. Subjects received infusions of either placebo at weeks 0, 2, 6, 12, 18 and 5 mg/kg infliximab at weeks 24, 26, 30 and every 6 weeks through week 96, or 5 mg/kg infliximab at weeks 1, 2, 6, 12, 18 and every 6 weeks through week 96
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ankylosing Spondylitis
Keywords
Ankylosing Spondylitis, infusion
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
279 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
infliximab
Primary Outcome Measure Information:
Title
The primary endpoint of this study was the proportion of subjects who achieved an ASAS 20 response at week 24.
Secondary Outcome Measure Information:
Title
The change from baseline in BASFI at week 24, the proportion of subjects who achieved an AS major clinical response at week 24, and the change from baseline in the physical component summary score of the SF-36 at week 24
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Have had a diagnosis of definite Akylosing Spondylitis for at least 3 months prior to screening
Have active disease with spinal pain
receiving or intolerant to standard anti-inflammatory agents
Exclusion Criteria:
Have Rheumatoid Arthritis, systemic lupus erythematosus, or other inflammatory rheumatic disease
Have a documented history of fibromyalgia
Have total ankylosis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Centocor, Inc. Clinical Trial
Organizational Affiliation
Centocor, Inc.
Official's Role
Study Director
12. IPD Sharing Statement
Citations:
PubMed Identifier
16874778
Citation
van der Heijde D, Han C, DeVlam K, Burmester G, van den Bosch F, Williamson P, Bala M, Han J, Braun J. Infliximab improves productivity and reduces workday loss in patients with ankylosing spondylitis: results from a randomized, placebo-controlled trial. Arthritis Rheum. 2006 Aug 15;55(4):569-74. doi: 10.1002/art.22097.
Results Reference
result
PubMed Identifier
16646033
Citation
Braun J, Landewe R, Hermann KG, Han J, Yan S, Williamson P, van der Heijde D; ASSERT Study Group. Major reduction in spinal inflammation in patients with ankylosing spondylitis after treatment with infliximab: results of a multicenter, randomized, double-blind, placebo-controlled magnetic resonance imaging study. Arthritis Rheum. 2006 May;54(5):1646-52. doi: 10.1002/art.21790.
Results Reference
result
PubMed Identifier
15692973
Citation
van der Heijde D, Dijkmans B, Geusens P, Sieper J, DeWoody K, Williamson P, Braun J; Ankylosing Spondylitis Study for the Evaluation of Recombinant Infliximab Therapy Study Group. Efficacy and safety of infliximab in patients with ankylosing spondylitis: results of a randomized, placebo-controlled trial (ASSERT). Arthritis Rheum. 2005 Feb;52(2):582-91. doi: 10.1002/art.20852.
Results Reference
result
PubMed Identifier
32993799
Citation
Webers C, Stolwijk C, Schiepers O, Schoonbrood T, van Tubergen A, Landewe R, van der Heijde D, Boonen A. Infliximab treatment reduces depressive symptoms in patients with ankylosing spondylitis: an ancillary study to a randomized controlled trial (ASSERT). Arthritis Res Ther. 2020 Sep 29;22(1):225. doi: 10.1186/s13075-020-02305-w.
Results Reference
derived
PubMed Identifier
18759257
Citation
Braun J, Deodhar A, Dijkmans B, Geusens P, Sieper J, Williamson P, Xu W, Visvanathan S, Baker D, Goldstein N, van der Heijde D; Ankylosing Spondylitis Study for the Evaluation of Recombinant Infliximab Therapy Study Group. Efficacy and safety of infliximab in patients with ankylosing spondylitis over a two-year period. Arthritis Rheum. 2008 Sep 15;59(9):1270-8. doi: 10.1002/art.24001.
Results Reference
derived
Links:
URL
http://filehosting.pharmacm.com/DownloadService.ashx?client=CTR_JNJ_6051&studyid=154&filename=CR004792_CSR.pdf
Description
A Randomized, Double-blind Trial of the Efficacy of REMICADE� (Infliximab) Compared with Placebo in Subjects with Ankylosing Spondylitis Receiving Standard Anti-inflammatory Drug Therapy
URL
http://filehosting.pharmacm.com/DownloadService.ashx?client=CTR_JNJ_6051&studyid=154&filename=CR004792_REF1.pdf
Description
| A Randomized, Double-blind Trial of the Efficacy of REMICADE® (Infliximab) Compared with Placebo in Subjects with Ankylosing Spondylitis Receiving Standard Anti-inflammatory Drug Therap
Learn more about this trial
A Study of Infliximab (Remicade) in Patients With Ankylosing Spondylitis.
We'll reach out to this number within 24 hrs