Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2017 Feb;27(2):127-143.
doi: 10.1080/13543776.2017.1252753. Epub 2016 Nov 7.

Inhibitors of JAK-family kinases: an update on the patent literature 2013-2015, part 1

Affiliations
Review

Inhibitors of JAK-family kinases: an update on the patent literature 2013-2015, part 1

Jason G Kettle et al. Expert Opin Ther Pat. 2017 Feb.

Abstract

Janus kinases (JAKs) are a family of four enzymes; JAK1, JAK2, JAK3 and tyrosine kinase 2 (TYK2) that are critical in cytokine signalling and are strongly linked to both cancer and inflammatory diseases. There are currently two launched JAK inhibitors for the treatment of human conditions: tofacitinib for Rheumatoid arthritis (RA) and ruxolitinib for myeloproliferative neoplasms including intermediate or high risk myelofibrosis and polycythemia vera. Areas covered: This review covers patents claiming activity against one or more JAK family members in the period 2013-2015 inclusive, and covers 95 patents from 42 applicants, split over two parts. The authors have ordered recent patents according to the primary applicant's name, with part 1 covering A through to I. Expert opinion: Inhibition of JAK-family kinases is an area of growing interest, catalysed by the maturity of data on marketed inhibitors ruxolitinib and tofacitinib in late stage clinical trials. Many applicants are pursuing traditional fast-follower strategies around these inhibitors, with a range of chemical strategies adopted. The challenge will be to show sufficient differentiation to the originator compounds, since dose limiting toxicities with such agents appear to be on target and mechanism-related and also considering that such agents may be available as generic compounds by the time follower agents reach market.

Keywords: JAK; JAK1 inhibitor; JAK2 inhibitor; JAK3 inhibitor; Janus kinase inhibitors; TYK2 inhibitor; myelofibrosis; oncology; rheumatoid arthritis; ruxolitinib; tofacitinib.

PubMed Disclaimer

MeSH terms

LinkOut - more resources