An updated patent review of rearranged during transfection (RET) kinase inhibitors (2022-present)

Daniel Armstrong1, Maha Hanafi1,2, Brendan Frett1

  • 1Department of Pharmaceutical Sciences, College of Pharmacy, University of Arkansas for Medical Sciences, Little Rock, AR, USA.

Abstract

Insights

Recent patents reveal novel small-molecule Rearranged during transfection (RET) inhibitors designed to overcome resistance and improve safety. These next-generation drugs offer a critical advancement in precision oncology for RET-driven cancers.

Area of Science:

  • Oncology
  • Pharmacology
  • Molecular Biology

Background:

  • Rearranged during transfection (RET) is a receptor tyrosine kinase vital for cell signaling.
  • Alterations in RET, including mutations and fusions, are implicated in cancer development.
  • Selective RET inhibitors have emerged as a precision oncology strategy.

Purpose of the Study:

  • To review recent innovations in RET inhibitor development.
  • To focus on small-molecule patents from 2022-2024.
  • To summarize structural classes, target profiles, and advantages of new compounds, especially in overcoming resistance.

Main Methods:

  • Comprehensive literature search using SciFinder and PatentScope.
  • Keywords: 'RET', 'RET inhibitor'.
  • Analysis of patented small-molecule RET inhibitors.

Main Results:

  • Identification of novel structural classes of RET inhibitors.
  • Characterization of target profiles for new compounds.
  • Highlighting compounds designed to address known resistance mechanisms.

Conclusions:

  • Next-generation RET inhibitors are crucial for advancing cancer treatment.
  • New patented compounds show promise in overcoming limitations of current therapies.
  • Continued development of selective RET inhibitors is a key frontier in precision oncology.

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