TY - JOUR
T1 - Standardisation of diet and exercise in clinical trials of NAFLD-NASH
T2 - Recommendations from the Liver Forum
AU - Liver Forum Standard of Care Working Group
AU - Glass, Oliver
AU - Filozof, Claudia
AU - Noureddin, Mazen
AU - Berner-Hansen, Mark
AU - Schabel, Elmer
AU - Omokaro, Stephanie O.
AU - Schattenberg, Jörn M.
AU - Barradas, Katherine
AU - Miller, Veronica
AU - Francque, Sven
AU - Abdelmalek, Manal F.
N1 - Funding Information:
In the past 24 months, The Forum for Collaborative Research has received unrestricted educational or research support from the following: 3-V Biosciences; Abbott Molecular; AbbVie; Advanced Biological Laboratories; Afimmune; Aicuris; Allergan; Aligos Therapeutics; Altimmune; AMRA Medical; Arbutus Biopharma; Arrowhead Pharmaceuticals; Assembly Biosciences; Astellas; Astra-Zeneca; Biogen; Boehringer Ingelheim; Bristol-Myers Squib; Celgene; Chimerix; Cirius Therapeutics; Cocrystal Pharma, Inc.; Conatus Pharmaceuticals, Inc.; ConSynance; Covance; DDL Diagnostics; CTI Clinical Trial and Consulting Services; Cirius Therapeutics Inc.; ContraVir; Cymabay; DeuteRx; DiaPharma; DS Biopharma; Durect; EA Pharma Co., Ltd.; Echosens; Eli Lilly and Company; Enanta Pharmaceuticals, Inc.; Enyo Pharma; e.scopics; Exalenz; Ferring Pharmaceuticals; Fractyl; Galectin Therapeutics; Genentech; Genesis Imaging Services; Genfit; Genkyotex; Gilead Sciences; GlaxoSmithKline; Glympse Bio; Hepatitis B Foundation; HepQuant; HighTide Therapeutics; HistoIndex Pte Ltd; Humedics GmbH; ICON Clinical Research; Immuron; Intercept Pharmaceuticals; Inventiva; Ironwood Pharmaceuticals; Janssen; LabCorp; Madrigal Pharmaceuticals; Mallinckrodt Pharmaceuticals; MEDIAN Technologies; MediciNova; Medivir; Merck Laboratories; Metacrine; Microbiotix; Mirum; Morphic Therapeutic; Mylan; NGM Biopharmaceuticals; Nimbus Therapeutics; Nitto Denko Technical Corp; Nordic Bioscience; Northsea Therapeutics; Novartis; Novo Nordisk Inc.; Nusirt; OWL Metabolomics; Perspectum Diagnostics; Pfizer; Pliant Therapeutics; PPD Inc.; ProSciento; Quest Diagnostics; Raptor Pharmaceuticals; Resonance Health; Resoundant; Roche Molecular Systems; Roivant Sciences; RuiYi; SeraCare; Shire; Springbank Pharma; Somalogic; Syneos Health; Takeda; TARGET PharmaSolutions; Teva Pharmaceuticals; ViiV Healthcare; VLVBio; Zafgen; and Zealand Pharma.This work was also supported in part by the Duke Divisions of Gastroenterology and Integrative Medicine and NIH Grant U01DK061713. These funding sources had no role in the analysis, and interpretation of data, the writing of the manuscript or the decision to submit the article for publication.
Funding Information:
This work was also supported in part by the Duke Divisions of Gastroenterology and Integrative Medicine and NIH Grant U01DK061713 . These funding sources had no role in the analysis, and interpretation of data, the writing of the manuscript or the decision to submit the article for publication.
Publisher Copyright:
© 2020
PY - 2020/9
Y1 - 2020/9
N2 - Lifestyle modification is the foundation of treatment recommendations for non-alcoholic fatty liver disease (NAFLD) and non-alcoholic steatohepatitis (NASH). The design of clinical trials in NASH may be impeded by the lack of a systematic approach to identify and evaluate how lifestyle changes and/or modifications influence clinical trial outcomes and associated endpoints. Furthermore, there are additional uncertainties regarding the methods that can be utilised to better characterise and quantify lifestyle variables – which can influence disease activity and alter trial endpoints – to allow for comparisons of trial outcomes across different phases of research and/or within drug-classes. This summary by the Liver Forum's Standard of Care Working Group reviews currently available clinical data, identifies the barriers and challenges associated with the standard of care in NAFLD/NASH clinical trials, defines available assessments of lifestyle changes, and proposes approaches to better understand and define the influence of diet and exercise on NASH treatment in the context of different pharmacologic interventions. The ultimate objective is to propose tangible solutions which enable investigators, sponsors, and regulatory authorities to meaningfully interpret clinical trial outcomes and the impact of lifestyle modification on such outcomes as they pertain to phase I-IV clinical trials.
AB - Lifestyle modification is the foundation of treatment recommendations for non-alcoholic fatty liver disease (NAFLD) and non-alcoholic steatohepatitis (NASH). The design of clinical trials in NASH may be impeded by the lack of a systematic approach to identify and evaluate how lifestyle changes and/or modifications influence clinical trial outcomes and associated endpoints. Furthermore, there are additional uncertainties regarding the methods that can be utilised to better characterise and quantify lifestyle variables – which can influence disease activity and alter trial endpoints – to allow for comparisons of trial outcomes across different phases of research and/or within drug-classes. This summary by the Liver Forum's Standard of Care Working Group reviews currently available clinical data, identifies the barriers and challenges associated with the standard of care in NAFLD/NASH clinical trials, defines available assessments of lifestyle changes, and proposes approaches to better understand and define the influence of diet and exercise on NASH treatment in the context of different pharmacologic interventions. The ultimate objective is to propose tangible solutions which enable investigators, sponsors, and regulatory authorities to meaningfully interpret clinical trial outcomes and the impact of lifestyle modification on such outcomes as they pertain to phase I-IV clinical trials.
KW - Clinical studies
KW - Endpoints
KW - Fibrosis
KW - Lifestyle modifications
KW - Placebo effect
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U2 - 10.1016/j.jhep.2020.04.030
DO - 10.1016/j.jhep.2020.04.030
M3 - Review article
C2 - 32353483
AN - SCOPUS:85086407365
SN - 0168-8278
VL - 73
SP - 680
EP - 693
JO - Journal of Hepatology
JF - Journal of Hepatology
IS - 3
ER -