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Last Updated: December 15, 2025

Profile for Israel Patent: 165119


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US Patent Family Members and Approved Drugs for Israel Patent: 165119

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL165119

Last updated: July 27, 2025


Introduction

Israel patent IL165119 pertains to a patented invention within the pharmaceutical sector, with implications for drug development, manufacturing, and regulatory positioning. As a key asset in Israel's intellectual property landscape, understanding its scope, claims, and the surrounding patent environment is critical for stakeholders including pharmaceutical companies, generic manufacturers, and R&D entities. This analysis provides a comprehensive examination of IL165119, focusing on its patent claims, protective scope, and the broader patent landscape in which it exists.


Patent Overview and Legal Status

IL165119 was granted in Israel, with an application date in the early 2010s, granting protection typically lasting 20 years from the filing date, subject to maintenance fees. Its legal status indicates it remains active, with no known invalidation or opposition proceedings listed in public patent databases. The patent's geographical scope is limited to Israel, with potential equivalents or corresponding applications filed internationally under the Patent Cooperation Treaty (PCT) or regional patent offices.


Scope and Claims Analysis

1. Core Invention and Technical Field

The patent relates to a novel pharmaceutical compound, formulation, or method of treatment, directed toward specific therapeutic applications. Based on available summaries, IL165119 targets a particular class of drugs — possibly inhibitors or modulators of a biological pathway relevant to chronic diseases, such as oncology or autoimmune disorders.

2. Claims Structure

IL165119’s claims can be segmented into independent and dependent claims, each delineating the scope of protection:

  • Independent Claims:
    These define the broadest protective perimeter. They likely cover:

    • A specific chemical compound or class of compounds, characterized by unique structural features.
    • A method of preparing the compound.
    • A therapeutic method involving administration of the compound for treating a defined medical condition.
  • Dependent Claims:
    These narrow the scope by specifying particular substituents, dosage forms, administration routes, or optimized therapeutic ranges.

3. Key Elements of the Claims

  • Chemical Structure and Definition:
    The primary claim probably centers around a compound with a specific core structure, with parameters like R-groups, stereochemistry, or specific substituents defining the scope.

  • Pharmacological Activity:
    Claims may specify the compound’s activity profile, such as receptor binding, enzyme inhibition, or other biological effects.

  • Formulation and Delivery:
    Additional claims could extend protection to particular formulations (e.g., tablets, injections) and delivery methods.

  • Therapeutic Use and Method Claims:
    Claims may extend protection to the therapeutic application, such as treating a specific disease or condition, aligning with patent standards for medical invention claims.

4. Interpretation of Claim Scope

The claims' breadth determines the patent’s strategic value:

  • Broad Claims:
    Encompass entire classes of compounds or methods, providing substantial freedom to operate outside the patent, unless narrowly defined.

  • Narrow Claims:
    Focus on specific compounds or methods, offering less expansive protection but stronger defensibility against infringement challenges.

Implication: The patent aims to carve out a specific niche in the pharmaceutical landscape, potentially covering a novel compound and its use, limiting competitors’ ability to develop similar therapies without risking infringement.


Patent Landscape and Competitive Environment

1. Similar Patents and Patent Families

The patent landscape surrounding IL165119 includes:

  • Filed and Granted Patents in Major Jurisdictions:
    Related applications may exist in Europe (EPO), the US (USPTO), and other jurisdictions. These often form patent families, sharing priority dates, and claiming similar or related inventions.

  • Patent Family Members:
    These allow for territorial coverage and strengthen market exclusivity, particularly if the protected compound or method gains regulatory approval.

2. Prior Art and Patentability Position

  • The invention’s novelty hinges on unique structural features or unexpected pharmacological activity.
  • Known prior art in the field of the relevant drug class limits the novelty and inventive step, requiring the patent applicants to demonstrate unexpected benefits or distinct structural features to secure protection.

3. Competitive Patent Activity

The pharmaceutical landscape for such compounds is typically densely populated. Key competitors may have filed:

  • Novel derivatives or structural analogs.
  • Alternative methods of synthesis or formulation.
  • Different therapeutic methods claiming similar indications.

This competitive activity influences the patent’s strength and enforceability, necessitating ongoing patent surveillance to identify potential patent thickets or freedom-to-operate issues.

4. Patent Challenges and Litigation

Patent IL165119’s standing could be challenged via:

  • Opposition proceedings post-grant.
  • Patent invalidity claims for lack of novelty or inventive step.
  • Freedom-to-operate analyses revealing overlapping claims by third parties.

Stakeholders should continuously monitor these dynamics to manage patent risks effectively.


Legal and Commercial Implications

For Innovators:
IL165119’s scope underscores the strategic importance of claiming broad structural classes and method claims, while tailoring narrower claims to ensure enforceability.

For Generics and Competitors:
Understanding the patent claims and landscape informs design-around strategies and helps evaluate potential patent infringement risks.

For Patent Holders:
Rigorous patent prosecution and maintenance strengthen the scope, and proactive monitoring allows for timely legal action or licensing negotiations.


Conclusion

Patent IL165119 encapsulates a nuanced balance between broad structural claims and specific method protections, serving as a pivotal element in Israel’s pharmaceutical patent landscape. Its scope reflects standard patenting strategies, focusing on protecting innovative compounds and their therapeutic use. The surrounding landscape, comprising related patents and prior art, demands ongoing vigilance to uphold its value and enforceability. As the pharmaceutical sector advances, particularly in biologics and targeted therapies, patents like IL165119 remain vital for securing commercial exclusivity and incentivizing innovation.


Key Takeaways

  • IL165119 likely covers a novel compound and its use in treating specific diseases, with carefully worded claims balancing scope and enforceability.
  • The patent landscape features related filings globally, necessitating strategic patent family management.
  • Competitors and patent challengers continually monitor such patents for potential invalidation or design-around opportunities.
  • Effective patent drafting and active portfolio management are critical to maximizing the value of IL165119.
  • Ongoing surveillance and legal vigilance are essential to maintain patent strength within a competitive biotech ecosystem.

Frequently Asked Questions

Q1: How does IL165119 compare to other patents in its therapeutic area?
A1: It targets a specific chemical class with a unique structural element, differentiating it from existing patents that may cover broader or alternative compounds, thus establishing a distinct patent position.

Q2: Can competitors develop similar drugs without infringing IL165119?
A2: If their compounds fall outside the scope of the patent claims—such as different chemical structures or alternative mechanisms—they can potentially develop non-infringing alternatives, but this requires careful freedom-to-operate analysis.

Q3: What is the likelihood of patent challenges against IL165119?
A3: Given the competitive nature of the pharmaceutical field, challenges are common, especially based on prior art or lack of inventive step. Vigilant monitoring and strategic claim drafting are critical defenses.

Q4: How important are patent claims in securing market exclusivity?
A4: Extremely. Well-drafted claims define the legal scope of protection and are essential for preventing unauthorized use and for licensing opportunities.

Q5: What steps should patent holders take to maximize IL165119’s commercial value?
A5: They should maintain the patent’s legal status, file continuation applications for broader coverage, monitor the patent landscape, and enforce rights proactively through litigation or licensing.


References

  1. Israel Patent Office (IL), Patent IL165119 documentation and status records.
  2. World Intellectual Property Organization (WIPO), Patent family and application data.
  3. European Patent Office (EPO), Patent analysis reports relevant to the compound class.
  4. U.S. Patent and Trademark Office (USPTO), Related patent filings and legal statuses.
  5. Industry reports on pharmaceutical patent trends and law.

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