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Exenatide once weekly over 2 years as a potential disease-modifying treatment for Parkinson's disease: protocol for a multicentre, randomised, double blind, parallel group, placebo controlled, phase 3 trial: The 'Exenatide-PD3' study.
Vijiaratnam, Nirosen; Girges, Christine; Auld, Grace; Chau, Marisa; Maclagan, Kate; King, Alexa; Skene, Simon; Chowdhury, Kashfia; Hibbert, Steve; Morris, Huw; Limousin, Patricia; Athauda, Dilan; Carroll, Camille B; Hu, Michele T; Silverdale, Monty; Duncan, Gordon W; Chaudhuri, Ray; Lo, Christine; Del Din, Silvia; Yarnall, Alison J; Rochester, Lynn; Gibson, Rachel; Dickson, John; Hunter, Rachael; Libri, Vincenzo; Foltynie, Thomas.
Afiliação
  • Vijiaratnam N; Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, London, UK.
  • Girges C; National Hospital for Neurology and Neurosurgery, London, UK.
  • Auld G; Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, London, UK.
  • Chau M; National Hospital for Neurology and Neurosurgery, London, UK.
  • Maclagan K; The Comprehensive Clinical Trials Unit, UCL, London, UK.
  • King A; The Comprehensive Clinical Trials Unit, UCL, London, UK.
  • Skene S; The Comprehensive Clinical Trials Unit, UCL, London, UK.
  • Chowdhury K; The Comprehensive Clinical Trials Unit, UCL, London, UK.
  • Hibbert S; Surrey Clinical Trials Unit, University of Surrey, Guildford, UK.
  • Morris H; Department of Clinical & Experimental Medicine, University of Surrey, Guildford, UK.
  • Limousin P; The Comprehensive Clinical Trials Unit, UCL, London, UK.
  • Athauda D; The Comprehensive Clinical Trials Unit, UCL, London, UK.
  • Carroll CB; Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, London, UK.
  • Hu MT; National Hospital for Neurology and Neurosurgery, London, UK.
  • Silverdale M; Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, London, UK.
  • Duncan GW; National Hospital for Neurology and Neurosurgery, London, UK.
  • Chaudhuri R; Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, London, UK.
  • Lo C; National Hospital for Neurology and Neurosurgery, London, UK.
  • Del Din S; Applied Parkinson's Research Group, University of Plymouth, Plymouth, UK.
  • Yarnall AJ; University Hospitals Plymouth NHS Trust, Plymouth, UK.
  • Rochester L; Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, Oxfordshire, UK.
  • Gibson R; Oxford Parkinson's Disease Centre, University of Oxford, Oxford, UK.
  • Dickson J; Department of Clinical Neurology, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Hunter R; Department of Neurology and Neurosurgery, University of Manchester, Greater Manchester, UK.
  • Libri V; Western General Hospital, NHS Lothian, Edinburgh, UK.
  • Foltynie T; University of Edinburgh, Edinburgh, UK.
BMJ Open ; 11(5): e047993, 2021 05 28.
Article em En | MEDLINE | ID: mdl-34049922
ABSTRACT

INTRODUCTION:

Parkinson's disease (PD) is a common neurodegenerative disorder with substantial morbidity. No disease-modifying treatments currently exist. The glucagon like peptide-1 receptor agonist exenatide has been associated in single-centre studies with reduced motor deterioration over 1 year. The aim of this multicentre UK trial is to confirm whether these previous positive results are maintained in a larger number of participants over 2 years and if effects accumulate with prolonged drug exposure. METHODS AND

ANALYSIS:

This is a phase 3, multicentre, double-blind, randomised, placebo-controlled trial of exenatide at a dose of 2 mg weekly in 200 participants with mild to moderate PD. Treatment duration is 96 weeks. Randomisation is 11, drug to placebo. Assessments are performed at baseline, week 12, 24, 36, 48, 60, 72, 84 and 96 weeks.The primary outcome is the comparison of Movement Disorders Society Unified Parkinson's Disease Rating Scale part 3 motor subscore in the practically defined OFF medication state at 96 weeks between participants according to treatment allocation. Secondary outcomes will compare the change between groups among other motor, non-motor and cognitive scores. The primary outcome will be reported using descriptive statistics and comparisons between treatment groups using a mixed model, adjusting for baseline scores. Secondary outcomes will be summarised between treatment groups using summary statistics and appropriate statistical tests to assess for significant differences. ETHICS AND DISSEMINATION This trial has been approved by the South Central-Berkshire Research Ethics Committee and the Health Research Authority. Results will be disseminated in peer-reviewed journals, presented at scientific meetings and to patients in lay-summary format. TRIAL REGISTRATION NUMBERS NCT04232969, ISRCTN14552789.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson Tipo de estudo: Clinical_trials / Guideline / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson Tipo de estudo: Clinical_trials / Guideline / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article