An Observational Study on Patients With Rheumatoid Arthritis Treated With MabThera (Rituximab)

NCT ID: NCT01075477

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

151 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-09-30

Study Completion Date

2011-12-31

Brief Summary

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This observational study will assess the execution, efficacy and safety of treatment with MabThera in patients with rheumatoid arthritis. Data from patients receiving MabThera according to local treatment guidelines will be collected for 29 months. Target sample size is 100-200 patients.

Detailed Description

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Conditions

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Rheumatoid Arthritis

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Cohort

rituximab [Mabthera/Rituxan]

Intervention Type DRUG

As prescribed by physician

Interventions

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rituximab [Mabthera/Rituxan]

As prescribed by physician

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* adult patients, \>/= 18 years of age
* rheumatoid arthritis
* treatment with rituximab

Exclusion Criteria

* unable/unwilling to give informed consent to data collection
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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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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Hämeenlinna, , Finland

Site Status

Helsinki, , Finland

Site Status

Joensuu, , Finland

Site Status

Jyväskylä, , Finland

Site Status

Paimio, , Finland

Site Status

Riihimäki, , Finland

Site Status

Seinäjoki, , Finland

Site Status

Tampere, , Finland

Site Status

Countries

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United States Finland

Other Identifiers

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ML22609

Identifier Type: -

Identifier Source: org_study_id