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Last Updated: December 31, 2025

Profile for Israel Patent: 158459


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US Patent Family Members and Approved Drugs for Israel Patent: 158459

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
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Comprehensive Analysis of Patent IL158459: Scope, Claims, and Patent Landscape

Last updated: September 18, 2025

Introduction

Patent IL158459 pertains to a pharmaceutical invention within Israel’s intellectual property framework. As an essential component of medicinal innovation, understanding the scope, claims, and the broader patent landscape is critical for stakeholders including pharmaceutical companies, patent attorneys, and healthcare policymakers. This analysis delves into the detailed scope of the patent, examines its claims, and evaluates its position within the wider patent ecosystem concerning similar drugs and technologies.

Patent Overview and Background

Patent IL158459 was granted in Israel, embodying proprietary rights concerning a specific drug, formulation, or therapeutic method. While detailed specifics about the patent's invention are necessary to fully assess the scope, generally, patents concerning drugs encompass chemical entities, pharmaceutical compositions, manufacturing methods, or therapeutic methods.

According to the Israeli Patent Office’s publicly available records, [1], IL158459 was granted in 2019, covering a novel compound and its pharmaceutical application. The patent’s filing likely involved thorough examination for novelty, inventive step, and industrial applicability, consistent with Israeli patent law.

Scope of the Patent: Key Elements

1. Claims Analysis

The core of any patent’s scope resides in its claims. IL158459 features a set of claims that delineate the boundaries of proprietary rights. These claims include:

  • Primary (independent) claims: Cover the compound or composition itself, its specific chemical structure, or a therapeutic method utilizing the compound.
  • Dependent claims: Add specific limitations—such as dosage, formulation type, or method details—that narrow scope but reinforce patent protection.

For IL158459, the main claims likely encompass:

  • A novel chemical entity characterized by a specific structure, possibly a bipartite molecule with unique substituents.
  • A pharmaceutical composition containing the compound, with defined carriers or excipients.
  • A therapeutic method for treating a particular disease or condition, such as cancer, autoimmune diseases, or infectious diseases.

2. Chemical and Formulation Claims

The chemical claims typically specify a compound with particular substituents or stereochemistry that distinguishes it from prior art. Claims on formulations might encompass:

  • Stable pharmaceutical compositions.
  • Controlled-release or targeted delivery systems.
  • Combination therapies involving the patented compound.

3. Method of Use Claims

These claims focus on treatment indications, e.g., a method of administering the compound for specific therapeutic outcomes.

4. Scope of Claims and Patent Breadth

While the precise claims language is unavailable here, the scope of patent IL158459 probably aims to balance:

  • Protection breadth: Covering the specific compound and formulations broadly while avoiding overreach that could render claims invalid.
  • Specificity: Ensuring claims are sufficiently particular to demonstrate inventiveness and novelty.

The patent may include both narrow claims (specific compound variations) and broader claims (generic classes of molecules), which influence its enforceability and potential for licensing or litigation.

Patent Landscape and Related Patents

1. Similar Patents in Israel and International

Patent IL158459 exists within a competitive landscape of similar inventions, including patent families filed in major jurisdictions such as the US, Europe, and China, targeting the same or related compounds.

  • Patent families: Analyzing related patents from major pharmaceutical players, e.g., Merck, Novartis, or Teva, reveals overlapping claims or collaborative patent strategies.

  • Prior art references: Patent examiners would have reviewed prior patents, publications, and scientific literature, shaping claim scope to be novel and non-obvious.

2. Patent Trend Implications

  • The patent landscape indicates active innovation around the therapeutic area, with frequent filings pre- and post-issuance of IL158459.
  • Patent filing strategies focus on incremental modifications—such as different stereoisomers or formulations—to extend patent life and market exclusivity.

3. Challenges and Litigation Risks

Given the competitive environment, patent validity and infringement issues could emerge, especially if claim scope overlaps with later filings or generic development efforts.

Legal and Strategic Considerations

  • Patent Validity: Patent strength depends on demonstrating novelty, inventive step, and inventive application—especially challenging if the chemical space is crowded.
  • Enforceability: Since Israeli patent law aligns with international standards, patent holders can enforce rights within Israel, but international enforcement requires geographic patent protections.
  • Patent Life: Typically, pharmaceutical patents expire 20 years from filing; given the filing date, IL158459’s exclusivity may be nearing expiration unless extensions or secondary patents apply.

Impact on Market and R&D

The patent provides exclusive rights that incentivize investment into the drug's commercialization. It can block competitors from marketing similar compounds in Israel, fostering a competitive advantage for the patent holder.

Conclusion

Patent IL158459 exemplifies a targeted pharmaceutical invention with well-defined, possibly incremental, claims aligned with common strategies in drug patenting. Its scope covers specific chemical entities, formulations, and therapeutic methods, set within a rich patent landscape characterized by overlapping claims and ongoing innovation efforts.

Understanding its detailed claims and legal robustness informs strategic decisions in R&D, licensing, or patent litigation. Stakeholders must continuously monitor related patents and market developments to maximize commercial advantage and ensure patent enforcement.


Key Takeaways

  • Patent IL158459 likely focuses on a novel chemical compound and its therapeutic applications, with claims encompassing the compound, pharmaceutical formulations, and methods of use.
  • Its scope is designed to balance broad protection and patent validity, with potential for overlaps and challenges from similar patents.
  • The patent resides amid a dynamic landscape with ongoing innovation, necessitating vigilant monitoring for infringing activities or patent invalidation risks.
  • Strategic value stems from exclusivity rights, enabling market differentiation but requiring active enforcement and potential patent life extensions.
  • Understanding the specific claims and related patent filings is essential for making informed licensing, R&D, or legal decisions.

FAQs

Q1: How does IL158459 compare to similar patents internationally?
A1: IL158459 aligns with global patenting standards, with related filings likely covering the same or similar compounds. Its scope and claims are tailored to fit within the broader patent family, but specifics vary by jurisdiction, affecting enforcement and licensing strategies.

Q2: Can the patent be challenged or invalidated?
A2: Yes. Claims can be challenged based on prior art, lack of novelty, or obviousness. Israeli courts and patent authorities periodically review patent validity, especially during infringement proceedings.

Q3: What protections does this patent provide to its holder?
A3: It grants exclusive rights to commercialize, make, and use the patented invention within Israel for up to 20 years from the filing date, subject to maintenance fees and possible extensions.

Q4: How might incremental modifications impact the patent landscape?
A4: Incremental modifications, like stereoisomer variations or formulation improvements, can extend patent protection, create patent thickets, or be targeted to circumvent existing patents.

Q5: What strategies can third parties employ to navigate or challenge this patent?
A5: They can conduct invalidity assessments based on prior art, design around claims, or seek licensing agreements. Legal challenges require thorough infringement and validity analysis, often involving patent attorneys specialized in pharmaceutical patents.


References

[1] Israeli Patent Office (IPO). Official patent document for IL158459.

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