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Effect of Patient Cost Sharing on Treatment Discontinuation Among Rheumatoid Arthritis Patients

Bristol-Myers Squibb (BMS) logo

Bristol-Myers Squibb (BMS)

Status

Completed

Conditions

Rheumatoid Arthritis

Study type

Observational

Funder types

Industry

Identifiers

NCT01137851
IM101-256

Details and patient eligibility

About

The purpose of this study is to assess the impact of patient cost sharing on treatment discontinuation of biologic agents in patients with Rheumatoid Arthritis (RA)

Enrollment

3,940 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Patients diagnosed with Rheumatoid Arthritis (RA) who newly initiated a biologic DMARD (bDMARD) during a study timeframe of 1/01/06 to 3/31/09.

Inclusion Criteria:

  • 18 to 64 years of age at index date
  • Diagnosis of RA during the study period (ICD-9CM 714.xx)
  • Evidence of at least one biologic DMARD of interest during the study timeframe
  • Continuous enrollment during the study timeframe
  • Both medical and pharmacy benefits
  • No evidence of a claim for a bDMARD in the 6-month pre-period

Exclusion Criteria:

  • Patients are excluded if they have a diagnosis of psoriasis, psoriatic arthritis, ankylosing spondylitis, Crohn's disease, or ulcerative colitis at any time during the study timeframe; have a claim for Rituxan, IV etanercept, or IV adalimumab; or have Medicare or Medicaid during the study timeframe

Trial design

3,940 participants in 1 patient group

New to bDMARD
Description:
New to bDMARD RA patients with high and low cost share who continue or discontinue treatment

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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