Next-Generation Therapeutics for Inflammatory Bowel Disease.

Parambir S Dulai, William J Sandborn
Author Information
  1. Parambir S Dulai: Division of Gastroenterology, University of California at San Diego, La Jolla, CA, USA.
  2. William J Sandborn: Division of Gastroenterology, University of California at San Diego, La Jolla, CA, USA. wsandborn@ucsd.edu.

Abstract

Tumor necrosis factor (TNF) antagonists are the cornerstone of therapy for moderately to severely active inflammatory bowel disease (IBD). Although our understanding of pharmacokinetics, pharmacodynamics, and treatment optimization for these agents has evolved considerably over the past decade, a substantial majority of individuals fail to respond or lose response to TNF-antagonists over time. A need therefore remains for efficacious treatment options in these patients. Alternative immunological targets have now been identified, and several novel therapeutic agents are in development for IBD. In this review article, we discuss these novel therapeutic agents, with a particular focus on those demonstrated to be efficacious in phase 2 and 3 clinical trials. We further discuss considerations to be made when integrating these agents into routine practice over the next decade.

Keywords

References

  1. Clin Gastroenterol Hepatol. 2014 Sep;12(9):1443-51; quiz e88-9 [PMID: 24462626]
  2. Lancet. 2015 Nov 7;386(10006):1825-34 [PMID: 26342731]
  3. Gastroenterol Clin North Am. 2014 Sep;43(3):525-41 [PMID: 25110257]
  4. Clin Gastroenterol Hepatol. 2016 Nov;14 (11):1593-1601.e2 [PMID: 26917043]
  5. Lancet. 2008 Feb 23;371(9613):660-667 [PMID: 18295023]
  6. N Engl J Med. 2013 Aug 22;369(8):699-710 [PMID: 23964932]
  7. J Crohns Colitis. 2016 Apr;10 (4):402-9 [PMID: 26681763]
  8. N Engl J Med. 2012 Oct 18;367(16):1519-28 [PMID: 23075178]
  9. Aliment Pharmacol Ther. 2016 May;43(10 ):1090-102 [PMID: 27038247]
  10. N Engl J Med. 2012 Aug 16;367(7):616-24 [PMID: 22894574]
  11. N Engl J Med. 2015 Mar 19;372(12):1104-13 [PMID: 25785968]
  12. Gastrointest Endosc. 2015 Aug;82(2):246-55 [PMID: 26005012]
  13. J Clin Invest. 2001 Aug;108(4):601-9 [PMID: 11518734]
  14. Gastroenterology. 2014 Sep;147(3):618-627.e3 [PMID: 24859203]
  15. Am J Gastroenterol. 2015 Dec;110(12):1737-8 [PMID: 26673509]
  16. Lancet. 2014 Jul 26;384(9940):309-18 [PMID: 24814090]
  17. Clin Gastroenterol Hepatol. 2016 Feb;14 (2):242-50.e1-2 [PMID: 26432476]
  18. Inflamm Bowel Dis. 2015 Dec;21(12 ):2879-85 [PMID: 26288002]
  19. J Crohns Colitis. 2014 Nov;8(11):1516-22 [PMID: 24996483]
  20. Gastroenterology. 2015 Jun;148(7):1320-9.e3 [PMID: 25724455]
  21. Aliment Pharmacol Ther. 2016 Jan;43(1):30-51 [PMID: 26515897]
  22. N Engl J Med. 2013 Aug 22;369(8):711-21 [PMID: 23964933]
  23. Gut. 2014 Dec;63(12):1843-53 [PMID: 24970900]
  24. N Engl J Med. 2016 May 5;374(18):1754-62 [PMID: 27144850]

Grants

  1. T32 DK007202/NIDDK NIH HHS

MeSH Term

Antibodies, Monoclonal, Humanized
Biological Products
Cell Adhesion Molecules
Gastrointestinal Agents
Humans
Immunoglobulins
Indans
Inflammatory Bowel Diseases
Mucoproteins
Oligonucleotides
Oxadiazoles
Piperidines
Pyrimidines
Pyrroles
Tumor Necrosis Factor-alpha
Ustekinumab

Chemicals

Antibodies, Monoclonal, Humanized
Biological Products
Cell Adhesion Molecules
Gastrointestinal Agents
Immunoglobulins
Indans
MADCAM1 protein, human
Mucoproteins
Oligonucleotides
Oxadiazoles
Piperidines
Pyrimidines
Pyrroles
Tumor Necrosis Factor-alpha
tofacitinib
vedolizumab
Ustekinumab
etrolizumab
GED0301
ozanimod

Word Cloud

Created with Highcharts 10.0.0agentsIBDtreatmentdecadeefficaciousnoveltherapeuticdiscussTumornecrosisfactorTNFantagonistscornerstonetherapymoderatelyto severelyactiveinflammatoryboweldiseaseAlthoughunderstandingpharmacokineticspharmacodynamicsoptimizationevolvedconsiderablypastsubstantialmajorityindividualsfailrespondloseresponseTNF-antagoniststimeneedthereforeremainsoptionspatientsAlternativeimmunologicaltargetsnowidentifiedseveraldevelopmentreviewarticleparticularfocusdemonstratedphase23clinicaltrialsconsiderationsmadeintegratingroutinepracticenextNext-GenerationTherapeuticsInflammatoryBowelDiseaseBiologicsEtrolizumabTofacitinibUstekinumabVedolizumab

Similar Articles

Cited By