Multi-drug approaches to NASH: what's in the development pipeline?
- PMID: 31524533
- DOI: 10.1080/13543784.2020.1668926
Multi-drug approaches to NASH: what's in the development pipeline?
Abstract
Introduction: The pandemic of obesity over the last two decades has triggered a rise in the prevalence of nonalcoholic fatty liver disease (NAFLD). NAFLD is associated with liver-related and cardiovascular complications. Despite this, the first licensed drug for NAFLD is yet to be approved. Given the scale of the problem and unmet needs, there is a myriad of agents in the development pipeline.Areas covered: We discuss promising agents in early phase clinical trials and categorize these agents based on their action on steatosis, steatohepatitis, and fibrosis. Furthermore, given the multisystemic nature of NAFLD, we consider the effects of these agents on the liver, their cardiometabolic effects, and the potential future strategies of combination therapies.Expert opinion: The paradigm for the ideal drug is the targeting of both steatohepatitis and fibrosis and the amelioration of cardiometabolic risk factors. New drugs that confer benefit in nonalcoholic steatohepatitis (NASH) must also be tested for their effects on type 2 diabetes mellitus and cardiovascular disease. The treatment of NASH will become analogous to the treatment of hypertension; it is very likely that multiple classes of drugs targeting different mechanistic pathways will be necessary because no single agent is likely to control all aspects of this complex liver disease.
Keywords: NAFLD; NASH; diabetes; nonalcoholic fatty liver disease; nonalcoholic steatohepatitis; obesity.
Similar articles
-
Promising therapies for treatment of nonalcoholic steatohepatitis.Expert Opin Emerg Drugs. 2016 Sep;21(3):343-57. doi: 10.1080/14728214.2016.1220533. Epub 2016 Aug 28. Expert Opin Emerg Drugs. 2016. PMID: 27501374 Free PMC article. Review.
-
Statins: An Under-Appreciated Asset for the Prevention and the Treatment of NAFLD or NASH and the Related Cardiovascular Risk.Curr Vasc Pharmacol. 2018;16(3):246-253. doi: 10.2174/1570161115666170621082910. Curr Vasc Pharmacol. 2018. PMID: 28676019 Review.
-
Treatment of patients with type 2 diabetes and non-alcoholic fatty liver disease: current approaches and future directions.Diabetologia. 2016 Jun;59(6):1112-20. doi: 10.1007/s00125-016-3952-1. Epub 2016 Apr 21. Diabetologia. 2016. PMID: 27101131 Free PMC article. Review.
-
Pharmacological management of nonalcoholic fatty liver disease.Metabolism. 2016 Aug;65(8):1183-95. doi: 10.1016/j.metabol.2016.04.004. Epub 2016 May 21. Metabolism. 2016. PMID: 27301803 Review.
-
Pharmacological management of nonalcoholic fatty liver disease in type 2 diabetes.Expert Rev Clin Pharmacol. 2017 May;10(5):535-547. doi: 10.1080/17512433.2017.1300059. Epub 2017 Mar 6. Expert Rev Clin Pharmacol. 2017. PMID: 28276774 Review.
Cited by
-
A revisit of drugs and potential therapeutic targets against non-alcoholic fatty liver disease: learning from clinical trials.J Endocrinol Invest. 2023 Oct 15. doi: 10.1007/s40618-023-02216-y. Online ahead of print. J Endocrinol Invest. 2023. PMID: 37839037 Review.
-
Deciphering the relational dynamics of AF-2 domain of PAN PPAR through drug repurposing and comparative simulations.PLoS One. 2023 Mar 31;18(3):e0283743. doi: 10.1371/journal.pone.0283743. eCollection 2023. PLoS One. 2023. PMID: 37000796 Free PMC article. Clinical Trial.
-
CDCDB: A large and continuously updated drug combination database.Sci Data. 2022 Jun 2;9(1):263. doi: 10.1038/s41597-022-01360-z. Sci Data. 2022. PMID: 35654801 Free PMC article.
-
Emerging advances in the pharmacologic treatment of nonalcoholic steatohepatitis and related cirrhosis.Ann Gastroenterol. 2022 May-Jun;35(3):213-225. doi: 10.20524/aog.2022.0704. Epub 2022 Apr 7. Ann Gastroenterol. 2022. PMID: 35599922 Free PMC article. Review.
-
Protective Effects of Tiaoganquzhi Decoction in Treating inflammatory Injury of Nonalcoholic Fatty liver Disease by Promoting CGI-58 and Inhibiting Expression of NLRP3 Inflammasome.Front Pharmacol. 2022 May 2;13:851267. doi: 10.3389/fphar.2022.851267. eCollection 2022. Front Pharmacol. 2022. PMID: 35586044 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
