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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02622503
Other study ID # ML30146
Secondary ID
Status Completed
Phase N/A
First received December 2, 2015
Last updated December 12, 2016
Start date April 2008
Est. completion date August 2008

Study information

Verified date December 2016
Source Hoffmann-La Roche
Contact n/a
Is FDA regulated No
Health authority Finland: Finnish Medicines Agency
Study type Observational

Clinical Trial Summary

The purpose of the study is to obtain an overall picture of rituximab treatments and treatment responses in RA patients.


Recruitment information / eligibility

Status Completed
Enrollment 81
Est. completion date August 2008
Est. primary completion date August 2008
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Rheumatoid arthritis (RA) patients treated with rituximab in Finland

Exclusion Criteria:

Study Design

Observational Model: Case-Only, Time Perspective: Retrospective


Related Conditions & MeSH terms


Intervention

Drug:
Rituximab
This is an observational study. Patients with rheumatoid arthritis and having received treatment previously will be assessed for the treatment responses.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Hoffmann-La Roche

Country where clinical trial is conducted

Finland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Information on previous RA treatments 3 months No
Primary Information on rituximab treatment responses 3 months No
Primary Information on concomitant medications 3 months No
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