An Observational Study of MabThera/Rituxan (Rituximab) in Patients With Sero-Positive Rheumatoid Arthritis Who Are Non-Responders or Intolerant to a Single TNF-Inhibitor (PORTSMAB)
NCT ID: NCT01309282
Last Updated: 2016-08-12
Study Results
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View full resultsBasic Information
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COMPLETED
9 participants
OBSERVATIONAL
2010-07-31
2013-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Rituximab
Sero-positive \[Rheumatoid Factor (RF) and/or anti-Cyclic Citrullinated Peptide (CCP+)\] rheumatoid arthritis (RA) patients, who had initiated therapy with Rituximab (MabThera) following lack of response or intolerance to a single tumour necrosis factor (TNF)-inhibitor will be included in this arm
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Rheumatoid arthritis positive for rheumatoid factor and/or anti-CCP
* Non-responder or intolerant to single TNF-inhibitor therapy
* Initiating treatment with MabThera/Rituxan
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Hoffmann-La Roche
INDUSTRY
Responsible Party
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Principal Investigators
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Clinical Trials
Role: STUDY_DIRECTOR
Hoffmann-La Roche
Locations
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Lisbon, , Portugal
Countries
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Other Identifiers
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ML22935
Identifier Type: -
Identifier Source: org_study_id
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