New biologics and small molecules in inflammatory bowel disease: an update.
Crohn’s disease
JAK inhibitor
S1P modulator
anti-integrin
biologicals
inflammatory bowel disease
small molecules
therapy
ulcerative colitis
Journal
Therapeutic advances in gastroenterology
ISSN: 1756-283X
Titre abrégé: Therap Adv Gastroenterol
Pays: England
ID NLM: 101478893
Informations de publication
Date de publication:
2019
2019
Historique:
received:
02
01
2019
accepted:
03
04
2019
entrez:
18
6
2019
pubmed:
18
6
2019
medline:
18
6
2019
Statut:
epublish
Résumé
Inflammatory bowel disease (IBD) is a spectrum of immune-mediated inflammatory disorders with a complex multifactorial pathogenesis, where different pathways may predominate in different individuals. This complexity will most likely require a panoply of drugs targeting different pathways if one wants to treat to steroid-free sustained remission and mucosal healing. Presently, the mainstay of medical management of IBD is based on 5-aminosalicylates, corticosteroids, thiopurines, methotrexate, antitumor necrosis factor, anti-alpha4 beta7 (α4β7) integrin and anti-interleukin (IL)-12/IL-23 therapies. The discovery of new pathways involved in the pathogenesis of IBD resulted in new drugs targeting Janus kinase/signal transducers and activators of transcription, IL-6, spingosine-1-phosphate, and phosphodiesterase 4, among others. These new therapies might result in more advantageous safety profiles. Several of these new drugs have already been successfully tested in other inflammatory disorders, such as psoriasis or rheumatoid arthritis. In this review, evidence from phase II and phase III randomized controlled clinical trials in patients with IBD involving new biologicals and small molecules are summarized.
Identifiants
pubmed: 31205488
doi: 10.1177/1756284819853208
pii: 10.1177_1756284819853208
pmc: PMC6537282
doi:
Types de publication
Journal Article
Review
Langues
eng
Pagination
1756284819853208Déclaration de conflit d'intérêts
Conflict of interest statement: João Sabino has received speaker fees from AbbVie and Nestle Health Sciences. Bram Verstockt has received financial support for research from Pfizer; lecture fees from AbbVie, Ferring, Takeda Pharmaceuticals, Janssen and R-Biopharm AG; consultancy fees from Janssen. Marc Ferrante has received research grants from Janssen, Pfizer, and Takeda; consultancy fees from AbbVie, Boehringer-Ingelheim, Falk, Ferring, Janssen, Mitsubishi Tanabe, MSD, and Pfizer; speakers fees from AbbVie, Boehringer-Ingelheim, Chiesi, Falk, Ferring, Janssen, Mitsubishi Tanabe, MSD, Pfizer, and Tramedico. Séverine Vermeire has received grant support from AbbVie, MSD, Pfizer, J&J, and Takeda; received speaker fees from AbbVie, MSD, Takeda, Ferring, Dr. Falk Pharma, Hospira, Pfizer Inc., and Tillots; and served as a consultant for AbbVie, MSD, Takeda, Ferring, Genentech/Roche, Robarts Clinical Trials, Gilead, Celgene, Prometheus, Avaxia, Prodigest, Shire, Pfizer Inc, Galapagos, Mundipharma, Hospira, Celgene, Second Genome, and Janssen.
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