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A patent review of DNA polymerase theta (Polθ) targeted therapies (2019-2025)
Luyu Ma1, Mingjin Luo1, Hua Xiang1
1State Key Laboratory of Natural Medicines and Department of Medicinal Chemistry, School of Pharmacy, China Pharmaceutical University, Nanjing, China.
Introduction:
DNA Polymerase theta (Polθ), a critical multifunctional DNA repair enzyme in the alternative non-homologous end joining (alt-NHEJ) pathway, has recently emerged as a new promising synthetic lethal target for homologous recombination (HR) deficient cancers. Since the first-in-class Polθ polymerase inhibitor entered clinical trials in 2021, this field has witnessed explosive growth in interest, underscored by a surge in Polθ inhibitor patents and nine candidates progressing to clinical trials.
Areas Covered:
This comprehensive patent review focuses on structural features and biochemical profiles of both Polθ inhibitors reported between 2019 and 2025, leveraging patents retrieved from the databases of World Intellectual Property Organization (WIPO), United States Patent and Trademark Office (USPTO), Cortellis Drug Discovery Intelligence, and China National Intellectual Property Administration (CNIPA).
Expert Opinion:
The rapid progress of Polθ inhibitors highlights their potential as a synthetic lethal strategy for HR-deficient cancers. Recently, an increasing number of patents and articles on inhibitors targeting Polθ have been published. At present, a total of nine Polθ inhibitors are under study in early clinical trials. Artios' Polθ inhibitor ART6043 has excellent clinical data. The results of these trials will influence the future development of Polθ inhibitors for HR-deficient cancers.
Insights
DNA Polymerase theta (Polθ) inhibitors are a promising synthetic lethal target for homologous recombination (HR) deficient cancers. This review covers Polθ inhibitor patents from 2019-2025, highlighting structural and biochemical profiles of nine clinical candidates.
Area of Science:
- Oncology
- Molecular Biology
- Drug Discovery
Background:
- DNA Polymerase theta (Polθ) is a key enzyme in DNA repair via the alt-NHEJ pathway.
- Polθ is a promising synthetic lethal target for homologous recombination (HR) deficient cancers.
- The field of Polθ inhibitors has seen significant growth since 2021, with nine candidates in clinical trials.
Purpose of the Study:
- To provide a comprehensive patent review of Polθ inhibitors.
- To analyze structural features and biochemical profiles of Polθ inhibitors.
- To assess the progress and potential of Polθ inhibitors in cancer therapy.
Main Methods:
- Patent retrieval from WIPO, USPTO, Cortellis, and CNIPA databases.
- Review of Polθ inhibitors reported between 2019 and 2025.
- Analysis of structural and biochemical data from retrieved patents.
Main Results:
- Explosive growth in Polθ inhibitor patents and clinical candidates.
- Nine Polθ inhibitors are currently in early clinical trials.
- Specific mention of ART6043 showing excellent clinical data.
Conclusions:
- Polθ inhibitors represent a rapidly advancing therapeutic strategy for HR-deficient cancers.
- Clinical trial results will be crucial for the future development of these inhibitors.
- The patent landscape indicates strong ongoing research and development in this area.
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