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ARTIOS Ofatumumab in relapsingMS patients moving from other therapies

  • Research type

    Research Study

  • Full title

    A single-arm, prospective, multicentre, open-label study to evaluate ofatumumab treatment effectiveness and patient reported outcomes in patients with relapsing multiple sclerosis transitioning from dimethyl fumarate or fingolimod therapy

  • IRAS ID

    275978

  • Contact name

    Jane Watson

  • Contact email

    jane.watson@novartis.com

  • Sponsor organisation

    Novartis Pharma AG

  • Eudract number

    2019-001341-40

  • Duration of Study in the UK

    3 years, 3 months, 4 days

  • Research summary

    The purpose of this study is to evaluate the safety and effectiveness of ofatumumab treatment in patients who are transitioning from their current multiple sclerosis (MS) treatment (DMF or fingolimod) due to breakthrough disease, onto ofatumumab. In addition, the study will explore the utility of biomarkers and digital tools in the assessment and treatment of people living with MS. The study will be run in 8 centred in the UK but only 6 have been selected at the time of submission. The remaining 2 will be submitted once known.

  • REC name

    West Midlands - Edgbaston Research Ethics Committee

  • REC reference

    20/WM/0082

  • Date of REC Opinion

    22 Apr 2020

  • REC opinion

    Further Information Favourable Opinion