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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

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....

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8166598/
https://www.ncbi.nlm.nih.gov/pubmed/34049922
http://dx.doi.org/10.1136/bmjopen-2020-047993
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author 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
author_facet 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
author_sort Vijiaratnam, Nirosen
collection PubMed
description 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 1:1, 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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spelling pubmed-81665982021-06-14 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 BMJ Open Neurology 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 1:1, 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. BMJ Publishing Group 2021-05-28 /pmc/articles/PMC8166598/ /pubmed/34049922 http://dx.doi.org/10.1136/bmjopen-2020-047993 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.
spellingShingle Neurology
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
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
title 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
title_full 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
title_fullStr 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
title_full_unstemmed 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
title_short 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
title_sort 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
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8166598/
https://www.ncbi.nlm.nih.gov/pubmed/34049922
http://dx.doi.org/10.1136/bmjopen-2020-047993
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