Baricitinib in rheumatoid arthritis: evidence-to-date and clinical potential
- PMID: 28255337
- PMCID: PMC5315227
- DOI: 10.1177/1759720X16687481
Baricitinib in rheumatoid arthritis: evidence-to-date and clinical potential
Abstract
Biologics have changed expectation and outcomes for rheumatoid arthritis (RA). However, the optimal duration and sequence of therapy for this disease has yet to be determined. Also, a significant number of patients do not satisfactorily respond to currently available therapies. The Janus kinase (JAK) inhibitors represent a new class of therapies for RA. These drugs work uniquely by inhibiting intracellular pathways thought to be important in the pathogenesis of RA. They are available as oral agents, which is also different from the currently available biologics. Baricitinib has now been evaluated in four phase III clinical trials, and although safety concerns cannot fully be answered until the drug is studied over longer periods of time, the data to date suggest that this drug with its once daily dosing, rapid onset of action and efficacy as monotherapy represents an important addition to the RA therapeutic armamentarium. Further study and experience will better define how baricitinib will be used and by which patients.
Keywords: Janus kinase inhibitors; baricitinib; rheumatoid arthritis.
Conflict of interest statement
Conflict of interest statement: Dr Kuriya: The Arthritis Society/Canadian Rheumatology Association Clinician Investigator Award; Advisory Board Member for F. Hoffman La Roche Inc, Abbott laboratories, Sanofi-Aventis Inc. Dr Keystone: Sources of funding for research, consulting agreements/advisory boards, speaker honoraria agreements: Amgen Inc., AstraZeneca Pharmaceuticals, Bristol-Myers Squibb, F. Hoffman La Roche Inc., Janssen Inc, Lilly Pharmaceuticals, Lilly Pharmaceuticals, Novartis Pharmaceuticals, Pfizer Pharmaceuticals, Sanofi-Aventis Inc.
References
-
- Tanaka Y., Yamaoka K. JAK inhibitor for treating rheumatoid arthritis: from basic to clinical. Mod Rheumatol 23: 415–424. - PubMed
-
- **Scott L. Tofacitinib: a review of its use in adult patients with rheumatoid arthritis. Drugs 73: 857–874. This is an inclusive review which includes preclinical observations and presentation of the important aspects of the tofacitinib clinical trials. - PubMed
-
- U.S. Food and Drug Administration. FDA approves Xeljanz for rheumatoid arthritis, http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm327152.htm (accessed 11 October 2016).
-
- Eli Lilly and Company. Lily and Incyte announce submission of new drug application to FDA for oral once-daily baricitinib for treatment of moderate-to-severe rheumatoid arthritis, https://investor.lilly.com/releasedetail.cfm?ReleaseID=950678 (accessed 15 October 2016).
Publication types
LinkOut - more resources
Full Text Sources
Other Literature Sources
