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An Observational Study to Describe in Routine Clinical Practice the Treatment Patterns of Usage of Biological DMARDs in RA Patients.

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Roche

Status

Completed

Conditions

Rheumatoid Arthritis

Treatments

Other: Routine clinical practice

Study type

Observational

Funder types

Industry

Identifiers

NCT02590562
ML28487

Details and patient eligibility

About

This observational study will describe the treatment patterns of usage of biological DMARDs in routine clinical practice and the demographics and RA disease characteristics in patients suffering from rheumatoid arthritis. Patients will be recruited and examined the same day when recruited. There will be no follow up visit or treatment period only one visit in this study.

Enrollment

808 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients at least 18 years of age.
  • Patients with a diagnosis of RA according to the revised ACR criteria.
  • Patients receiving treatment of launched biological DMARDs.

Exclusion criteria

  • Patients who received biological DMARDs due to clinical trials or biologics not launched.
  • Patients who are considered not appropriate for study due to other reasons at physicians' discretion.

Trial design

808 participants in 1 patient group

RA patients treated with routine clinical practice
Description:
Describe in routine clinical practice the treatment patterns of usage of biological DMARDs in patients suffering from RA including frequency of monotherapy, biological DMARDs usage status (types, dosage), concomitant DMARDs usage information (type and dosage)
Treatment:
Other: Routine clinical practice

Trial contacts and locations

15

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Data sourced from clinicaltrials.gov

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