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Assessment of Rituximab''s Immunomodulatory Synovial Effects (The ARISE Study) - Article


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Methotrexate Injection

Amethopterin; MTX Injection


Clinical Trial: Assessment of Rituximab''s Immunomodulatory Synovial Effects (The ARISE Study)

This study is currently recruiting patients.
Verified by University of California, San Diego September 2005

Sponsors and Collaborators: University of California, San Diego
Genentech
Information provided by: University of California, San Diego
ClinicalTrials.gov Identifier: NCT00147966

Purpose

Using repeated arthroscopic biopsies of patients with rheumatoid arthritis, we will assess changes in the immune response that occur as a result of treatment with rituximab.
Condition Intervention Phase
Rheumatoid Arthritis
active disease despite concomitant methotrexate
 Drug: arthroscopic biopsy
Phase II

MedlinePlus related topics:  Rheumatoid Arthritis

Study Type: Interventional
Study Design: Diagnostic, Non-Randomized, Open Label, Active Control, Single Group Assignment, Safety/Efficacy Study

Official Title: Assessment of the Immunomodulatory Effects of Rituximab in Seropositive Rheumatoid Arthritis Using Arthroscopic Synovial Biopsies

Eligibility

Ages Eligible for Study:  18 Years   -   75 Years,  Genders Eligible for Study:  Both
Criteria

Inclusion Criteria:

  • Active rheumatoid arthritis use of concomitant methotrexate

Exclusion Criteria:

  • Use of DMARDs/biologics other than methotrexate serious medical conditions that would preclude the use of the treating agent

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00147966

Arthur Kavanaugh, MD      858-657-7040    akavanaugh@ucsd.edu

California
      UCSD CIT, La Jolla,  California,  92093,  United States; Recruiting
Jessica Hallinan  858-657-7042    jhallinan@ucsd.edu 

Study chairs or principal investigators

Arthur Kavanaugh, MD,  Principal Investigator,  UCSD CIT   

More Information

Study ID Numbers:  041569
Last Updated:  September 6, 2005
Record first received:  September 2, 2005
ClinicalTrials.gov Identifier:  NCT00147966
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-09-13


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Page Updated: June 1, 2005
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