Your browser doesn't support javascript.
loading
Safety and efficacy of belimumab after B cell depletion therapy in systemic LUPUS erythematosus (BEAT-LUPUS) trial: statistical analysis plan.
Muller, Patrick; Chowdhury, Kashfia; Gordon, Caroline; Ehrenstein, Michael R; Doré, Caroline J.
Affiliation
  • Muller P; Comprehensive Clinical Trials Unit, Institute of Clinical Trials and Methodology, University College London, London, UK. p.muller@ucl.ac.uk.
  • Chowdhury K; Comprehensive Clinical Trials Unit, Institute of Clinical Trials and Methodology, University College London, London, UK.
  • Gordon C; Rheumatology Research Group, Institute of Inflammation and Ageing (IIA), University of Birmingham, Birmingham, UK.
  • Ehrenstein MR; Centre for Rheumatology, Division of Medicine, University College London, London, UK.
  • Doré CJ; Comprehensive Clinical Trials Unit, Institute of Clinical Trials and Methodology, University College London, London, UK.
Trials ; 21(1): 652, 2020 Jul 16.
Article in En | MEDLINE | ID: mdl-32677992
ABSTRACT

BACKGROUND:

There is limited evidence that rituximab, a B cell depletion therapy, is an effective treatment for systemic lupus erythematosus (SLE). Data on the mechanisms of B cell depletion in SLE indicate that the combination of rituximab and belimumab may be more effective than rituximab alone. The safety and efficacy of belimumab after B cell depletion therapy in systemic LUPUS erythematosus (BEAT-LUPUS) trial aims to determine whether belimumab is superior to placebo, when given 4-8 weeks after treatment with rituximab. This article describes the statistical analysis plan for this trial as an update to the published protocol. It is written prior to the end of patient follow-up, while the outcome of the trial is still unknown. DESIGN AND

METHODS:

BEAT-LUPUS is a randomised, double-blind, phase II trial of 52 weeks of belimumab versus placebo, initiated 4-8 weeks after rituximab treatment. The primary outcome is anti-dsDNA antibodies at 52 weeks post randomisation. Secondary outcomes include lupus flares and damage, adverse events, doses of concomitant medications, quality of life, and clinical biomarkers. We describe the trial's clinical context, outcome measures, sample size calculation, and statistical modelling strategy, and the supportive analyses planned to evaluate for mediation of the treatment effect through changes in concomitant medication doses and bias from missing data.

DISCUSSION:

The analysis will provide detailed information on the safety and effectiveness of belimumab. It will be implemented from July 2020 when patient follow-up and data collection is complete. TRIAL REGISTRATION ISRCTN 47873003 . Registered on 28 November 2016. EudracT 2015-005543-14 . Registered on 19 November 2018.
Subject(s)
Key words

Full text: 1 Database: MEDLINE Main subject: B-Lymphocytes / Antibodies, Monoclonal, Humanized / Lupus Erythematosus, Systemic Type of study: Clinical_trials / Diagnostic_studies / Guideline / Prognostic_studies Limits: Humans Language: En Journal: Trials Journal subject: MEDICINA / TERAPEUTICA Year: 2020 Type: Article Affiliation country: United kingdom

Full text: 1 Database: MEDLINE Main subject: B-Lymphocytes / Antibodies, Monoclonal, Humanized / Lupus Erythematosus, Systemic Type of study: Clinical_trials / Diagnostic_studies / Guideline / Prognostic_studies Limits: Humans Language: En Journal: Trials Journal subject: MEDICINA / TERAPEUTICA Year: 2020 Type: Article Affiliation country: United kingdom