A Retrospective Chart Review of MabThera (Rituximab) Treatment in Rheumatoid Arthritis (RA) Participants in Australia

NCT ID: NCT02564770

Last Updated: 2016-11-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

167 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-01-31

Study Completion Date

2012-02-29

Brief Summary

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This is a cross-sectional, observational study examining the factors leading to the therapeutic decision to use MabThera (rituximab) in participants with RA. Routine rheumatology clinical practice data of participants who are being or have been treated with rituximab for RA will be collected and analysed in this chart review.

Detailed Description

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Conditions

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Rheumatoid Arthritis

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

RETROSPECTIVE

Study Groups

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Rheumatoid arthritis (RA) participants

Participants who had been treated with rituximab for RA are reviewed retrospectively using chart review from Baseline until and their most recent visit to the rheumatologist prior to the conduct of the chart review.

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Greater than or equal to (\>=) 18 years of age at the time of data collection
* RA diagnosed by a rheumatologist
* Treatment with rituximab for RA

Exclusion Criteria

* Participants whose primary diagnosis and indication for rituximab treatment is a condition other than RA
* Participants who have been treated with an experimental agent for RA which is not currently approved for the treatment of RA in Australia
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Roche Products Pty Ltd (Australia)

UNKNOWN

Sponsor Role collaborator

Hoffmann-La Roche

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Clinical Trials

Role: STUDY_DIRECTOR

Hoffmann-La Roche

Locations

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Geelong, Victoria, Australia

Site Status

Countries

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Australia

Other Identifiers

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ML28321

Identifier Type: -

Identifier Source: org_study_id