Small molecule oral targeted therapies in ulcerative colitis.
Administration, Oral
Aged
Chronic Disease
/ drug therapy
Clinical Trials as Topic
Colitis, Ulcerative
/ drug therapy
Cyclic Nucleotide Phosphodiesterases, Type 4
/ drug effects
Drug Evaluation, Preclinical
/ methods
Humans
Immunomodulation
Incidence
Inflammatory Bowel Diseases
/ drug therapy
Janus Kinase Inhibitors
/ pharmacology
Janus Kinases
/ antagonists & inhibitors
Middle Aged
Molecular Targeted Therapy
/ methods
Phosphodiesterase 4 Inhibitors
/ pharmacology
Prevalence
Sphingosine-1-Phosphate Receptors
/ agonists
Journal
The lancet. Gastroenterology & hepatology
ISSN: 2468-1253
Titre abrégé: Lancet Gastroenterol Hepatol
Pays: Netherlands
ID NLM: 101690683
Informations de publication
Date de publication:
09 2020
09 2020
Historique:
received:
19
09
2019
revised:
04
11
2019
accepted:
11
11
2019
pubmed:
15
3
2020
medline:
15
9
2020
entrez:
15
3
2020
Statut:
ppublish
Résumé
The incidence and prevalence of ulcerative colitis are increasing globally. Although the exact cause and pathogenesis of this disease is unclear, research has led to a better understanding of the condition and to identification of new targets for therapy, which in turn has encouraged the development of new therapies. As well as biologic therapies, which have changed the way inflammatory bowel disease is managed, small molecules have been developed for the treatment of ulcerative colitis. These small molecule treatments are orally administered and are likely to bring a substantial shift in the way this chronic disease is treated. Oral therapies offer many advantages over infusion therapies, such as ease of use, increased acceptability by patients, and reduction of cost. This Review focuses not only on oral therapies that have been approved for use in ulcerative colitis, but also on those that are in development, providing a comprehensive overview for clinicians of available oral therapies and drugs that are likely to become available. We have also reviewed drugs that have shown promise in preclinical studies and could be effective future therapies.
Identifiants
pubmed: 32171056
pii: S2468-1253(19)30414-5
doi: 10.1016/S2468-1253(19)30414-5
pii:
doi:
Substances chimiques
Janus Kinase Inhibitors
0
Phosphodiesterase 4 Inhibitors
0
Sphingosine-1-Phosphate Receptors
0
Janus Kinases
EC 2.7.10.2
Cyclic Nucleotide Phosphodiesterases, Type 4
EC 3.1.4.17
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
850-861Informations de copyright
Copyright © 2020 Elsevier Ltd. All rights reserved.