Baricitinib therapy for Rheumatoid Arthritis: an Observational Study

  • Research type

    Research Study

  • Full title

    A Multinational, Prospective, Observational Study of the Effectiveness, Healthcare Resource Utilization and Costs in Patients with Rheumatoid Arthritis Receiving Baricitinib, Targeted Synthetic or Biologic Disease-Modifying Therapies

  • IRAS ID

    249435

  • Contact name

    Tom Sheeran

  • Contact email

    t.sheeran@nhs.net

  • Sponsor organisation

    Eli Lilly and Company

  • Duration of Study in the UK

    6 years, 3 months, 31 days

  • Research summary

    The purpose of this study is to assess the effectiveness of Olumiant (baricitinib) and certain other treatments for rheumatoid arthritis and the effect, if any, on physical functioning, quality of life, and pain associated with rheumatoid arthritis. The healthcare resources required for treating and managing rheumatoid arthritis and the associated costs will also be explored.

    This is an observational study. There are no experimental treatments involved, and there will be no additional tests or clinic visits required. Participants will only be undergoing standard of care treatment.

    About 200 clinics in 9 countries across different parts of the world will provide information on their participants for this study. There will be approximately 1840 participants in this study.

  • REC name

    South West - Frenchay Research Ethics Committee

  • REC reference

    18/SW/0214

  • Date of REC Opinion

    14 Sep 2018

  • REC opinion

    Favourable Opinion