Simvastatin in sight threatening Uveitis trial (SU)

  • Research type

    Research Study

  • Full title

    Can simvastatin significantly reduce the amount of immunosuppressive medication required by patients with sight threatening uveitis? A phase IIb, single site, randomized, placebo controlled, double blinded trial.

  • IRAS ID

    156966

  • Contact name

    Sue Lightman

  • Contact email

    s.lightman@ucl.ac.uk

  • Sponsor organisation

    UCL, Joint Research Office

  • Eudract number

    2014-003119-13

  • Clinicaltrials.gov Identifier

    NCT02252328

  • Duration of Study in the UK

    2 years, 7 months, 31 days

  • Research summary

    This study aims to examine the immunosupressive effect of oral simvastatin 80mg once a day among patients with uveitis who are receiving systemic corticosteroids. Recently it has been found that simvastatin has an immunosupressive effect in humans, results in greater control of systemic inflammation and slows the progression of conditions such as multiple sclerosis.

    This study will be conducted at Moorfields Eye Hospital and will include patients with uveitis who require systemic corticosteroids to control their ocular inflammation. Patients will be randomised to either receive either simvastatin or placebo, in addition to their immunosuppression treatment.
    The study will follow these patients for 24 months and explore whether the addition of simvastatin results in a greater tapering in systemic corticosteroids than placebo.

  • REC name

    London - Bloomsbury Research Ethics Committee

  • REC reference

    15/LO/0084

  • Date of REC Opinion

    11 Feb 2015

  • REC opinion

    Favourable Opinion