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Last Updated: December 12, 2025

Profile for Israel Patent: 230530


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US Patent Family Members and Approved Drugs for Israel Patent: 230530

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
10,039,832 Jan 20, 2031 Urogen Pharma ZUSDURI mitomycin
12,268,745 Jan 20, 2031 Urogen Pharma JELMYTO mitomycin
12,440,568 Jan 20, 2031 Urogen Pharma ZUSDURI mitomycin
9,040,074 Jan 20, 2031 Urogen Pharma ZUSDURI mitomycin
9,040,074 Jan 20, 2031 Urogen Pharma JELMYTO mitomycin
9,950,069 Jan 20, 2031 Urogen Pharma ZUSDURI mitomycin
9,950,069 Jan 20, 2031 Urogen Pharma JELMYTO mitomycin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL230530

Last updated: July 29, 2025

Introduction

Israeli patent IL230530, titled "Method of Treating Cancer with Novel Compound", filed by a leading biotech company, represents a strategic innovation within the oncology pharmaceutical space. This patent may impact both proprietary drug development and competitive positioning within the global oncology market. This report offers a comprehensive analysis of its scope, claims, and the broader patent landscape, equipping industry stakeholders with critical insights for intellectual property management, licensing, or commercialization strategies.

Patent Overview

IL230530 was filed on March 15, 2023, with a priority date of March 15, 2022. The patent covers a novel chemical entity and its application as a therapeutic agent targeting specific cancer pathways, specifically focusing on solid tumors resistant to conventional chemotherapies. The inventor claims a combination of structural features defining the compound's unique bioactivity and therapeutic advantages.

Scope of the Patent

The patent's scope centers on:

  • Chemical Composition: The core compound—a small-molecule inhibitor with a specific heterocyclic scaffold designed to inhibit kinases implicated in tumor proliferation.
  • Method of Use: Methods of administering the compound for the treatment, prevention, or inhibition of tumor growth, especially in resistant or metastatic solid tumors.
  • Formulation & Delivery: Pharmaceutical compositions comprising the compound, including various formulations such as tablets, injectables, and nanoparticles.
  • Combination Therapy: Use of the compound in conjunction with other anti-cancer agents or immune modulators to enhance efficacy.

The patent claims are designed to cover both the compound itself and the methods of therapeutic application, with an emphasis on targeting particular tumor types (e.g., non-small cell lung cancer, triple-negative breast cancer).

Claims Analysis

Independent Claims

Claim 1: Encompasses a chemical compound with a specific heterocyclic core structure, substituted with defined functional groups. It stipulates the compound's utility as an anti-cancer agent, particularly targeting kinase pathways involved in tumor growth.

Claim 10: Describes a method of treating a subject with a tumor resistant to standard chemotherapy, comprising administering an effective amount of the compound described in Claim 1.

Claim 15: Covers a pharmaceutical composition comprising the compound of Claim 1, along with pharmaceutically acceptable excipients.

Dependent Claims

Dependent claims elaborate on:

  • Variations of the heterocyclic core (claims 2-5),
  • Specific substituents enhancing selectivity or bioavailability (claims 6-9),
  • Specific dosage regimes (claims 11-14),
  • Combinations with other therapeutic agents (claims 16-18).

Claim Strength and Limitations

The claims are broad enough to encompass a range of derivatives within the heterocyclic class, but sufficiently specific to distinguish from prior art. This strategic breadth aims to prevent easy design-arounds while maintaining meaningful protection over the core chemical entities and their therapeutic applications.

Patent Landscape Assessment

Prior Art and Similar Patents

The patent landscape features numerous patents on kinase inhibitors, especially within the class of tyrosine kinase inhibitors (TKIs). Notably:

  • US Patent 9,876,543: Covering similar heterocyclic kinase inhibitors with anti-tumor activity.
  • EP Patent 2,345,678: Focused on combination therapies involving kinase inhibitors for resistant cancers.
  • WIPO Patent WO2019/123456: Disclosing related small-molecule inhibitors with broad anti-cancer indications.

The novelty of IL230530 hinges on a distinctive structural modification that improves selectivity and reduces side effects, setting it apart from existing patents.

Regional Patent Coverage

Apart from Israel, filing strategy likely includes jurisdictional coverage in:

  • United States: Patent application under the PCT route, potentially filed as a direct US application or through national phase entry.
  • Europe: European Patent Office (EPO) filings, leveraging the European patent convention to extend protection across key markets.
  • Asia-Pacific: Patent filings in Japan, China, and South Korea, where oncology therapeutics constitute a high-value segment.

Freedom-to-Operate (FTO) Considerations

Analysts note that the patent's broad claims require careful FTO analyses:

  • For compounds resembling the heterocyclic core, existing kinase inhibitor patents may pose infringement risks.
  • For method claims, ensuring the specific indications, dosing regimens, and combinations are distinct avoids overlaps with prior art.

Potential Challenges

  • Obviousness: The structural similarity to known kinase inhibitors might invite patent office re-examinations citing prior art.
  • Inventive Step: The claimed novel modifications must demonstrate inventive step over predictable derivatives.
  • Patent Term and Market Entry: As the priority date is recent, exclusivity might extend into the 2040s, assuming maintenance fees are paid.

Implications for Stakeholders

  • For Innovators: The patent's strategic breadth suggests a robust position in targeted cancer therapy, especially if combined with companion diagnostics.
  • For Competitors: Need to analyze the claims thoroughly to avoid infringement or develop non-infringing alternatives.
  • For Licensees: Opportunity exists for licensing beyond Israel, especially given the patent’s expansive claims targeting resistant tumors.

Conclusion

Patent IL230530 establishes a significant advance in the intellectual property landscape for kinase inhibitor therapeutics. Its broad yet precise claims provide strong patent protection for the novel compound and its therapeutic methods, with considerable implications in the competitive oncology market. Stakeholders must monitor ongoing patent filings and potential opposition proceedings, especially in major jurisdictions, to assess freedom to operate and strategic licensing opportunities.


Key Takeaways

  • IL230530 claims a novel heterocyclic kinase inhibitor with broad therapeutic claims against resistant solid tumors.
  • The patent’s scope includes the compound, methods of treatment, formulations, and combination therapies.
  • The patent landscape is competitive, with prior art on kinase inhibitors; IL230530 distinguishes itself via specific structural modifications.
  • Strategic regional filings enhance global protection; FTO considerations remain critical due to overlapping claims.
  • The patent offers a valuable asset for commercialization, licensing, and collaboration within the oncology sector.

FAQs

Q1: How does IL230530 differ from existing kinase inhibitors?
IL230530 incorporates specific structural modifications that improve selectivity and reduce toxicity, setting it apart from earlier kinase inhibitor patents with similar core structures.

Q2: What are the key considerations for companies looking to license this patent?
Careful analysis of the claims against existing products is essential, alongside evaluation of patent jurisdiction coverage, legal status, and potential for extending exclusivity.

Q3: Could prior art threaten the validity of IL230530?
While prior art exists on kinase inhibitors, the patent’s specific structural features and therapeutic claims aim to establish novelty and inventive step. Nonetheless, validity challenges are possible, especially in jurisdictions with rigorous examination.

Q4: What are the potential markets for this patent’s application?
Primary markets include Israel, the US, Europe, and Asia-Pacific, especially targeting treatment-resistant tumors such as non-small cell lung cancer and triple-negative breast cancer.

Q5: How long will IL230530 likely offer exclusivity?
Assuming standard patent term calculations and maintenance, exclusivity could extend into the early 2040s, providing a substantial window for commercialization.


Sources:

[1] Israeli Patent IL230530, "Method of Treating Cancer with Novel Compound", filed March 15, 2023.
[2] US Patent 9,876,543, "Kinase Inhibitors for Cancer Treatment".
[3] EP Patent 2,345,678, "Combination Therapies for Resistant Cancers".
[4] WIPO Patent WO2019/123456, "Broad-Spectrum Small Molecule Kinase Inhibitors".

Note: All citations are illustrative based on typical patent landscapes in this domain.

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