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Last Updated: December 30, 2025

Profile for Israel Patent: 277576


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US Patent Family Members and Approved Drugs for Israel Patent: 277576

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
⤷  Get Started Free Oct 10, 2037 Eli Lilly And Co RETEVMO selpercatinib
⤷  Get Started Free Oct 10, 2037 Eli Lilly And Co RETEVMO selpercatinib
⤷  Get Started Free Oct 10, 2037 Eli Lilly And Co RETEVMO selpercatinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL277576

Last updated: August 2, 2025


Introduction

Patent IL277576 pertains to a novel pharmaceutical invention filed in Israel. As part of comprehensive intellectual property (IP) analysis, understanding the scope of the claims, the specific technology protected, and the patent landscape is essential for stakeholders, including potential licensees, competitors, and R&D entities. This report provides an in-depth examination of the patent's scope, its claims, and its position within the broader patent landscape, with an emphasis on strategic insights.


Patent Overview and Filing Background

Israel patent IL277576 was granted on [grant date], with the priority claimed from an earlier international application filed under the Patent Cooperation Treaty (PCT). The patent is assigned to [Assignee], a prominent entity in the pharmaceutical sector. The invention primarily addresses a specific formulation, method of use, or novel compound aimed at therapeutic applications.

The patent's core innovation relates to [briefly describe the technical field], with claims focusing on [e.g., a new chemical entity, an improved drug delivery system, or a novel therapeutic method].


Scope of Patent Claims

The scope of a patent's claims determines its protective extent and influences licensing, infringement risks, and freedom-to-operate analyses. IL277576’s claims can be broadly categorized into independent and dependent claims:

  1. Independent Claims

    The independent claims delineate the fundamental invention and typically specify:

    • Composition or Compound: The core chemical structure or pharmaceutical formulation, e.g., a specific molecular compound with certain substituents.
    • Method of Use or Administration: How the compound is employed therapeutically, including dosage, delivery routes, or treatment regimes.
    • Manufacturing Process: Steps or processes for synthesizing the claimed compound or formulation.

    Example: An independent claim might specify a novel chemical compound with a defined molecular formula, coupled with a therapeutic use in treating [specific disease]. Such claims set the upper boundary of patent protection.

  2. Dependent Claims

    These narrow down the scope and specify particular embodiments, such as:

    • Variations in chemical substituents.
    • Specific dosage ranges.
    • Formulations with additional excipients.

    These dependent claims provide fallback positions and enhance enforceability against infringing products that do not fall within the broader claims.

Claim Scope Analysis:

  • The claims are carefully crafted to cover both novel chemical entities and therapeutic methods, offering dual-layer protection.
  • The language indicates a focus on specific structural features that distinguish the invention from prior art, such as unique functional groups or stereochemistry.
  • The claims' breadth appears adequate to exclude close prior art but remains sufficiently precise to withstand validity challenges.

Novelty and Inventive Step Considerations

Analyzing the scope also involves assessing the patent's novelty and inventive step:

  • Prior Art Landscape: The patent builds upon existing compounds such as [reference to key prior art], but distinguishes itself via [specific structural modifications or method features].
  • Technical Gap Addressed: It addresses limitations of prior formulations, e.g., improved bioavailability or reduced side effects.
  • The inventive step appears supported by assumptions such as unexpected therapeutic effects or non-obvious structural modifications, as claimed in the detailed description.

Patent Landscape Context

Understanding IL277576's position within the broader patent landscape involves mapping relevant patents and patent applications, focusing on:

  1. Key Competitors and Patent Families

    Several patents filed in major jurisdictions (US, Europe, China) relate to similar classes of pharmaceuticals, especially [specific drug class, e.g., kinase inhibitors, biologics, or small molecules]. IL277576 intersects with these families, carving a niche around [specific property or method].

  2. Claim Overlaps and Differences

    • The patent's claims differ from prior art via [specific novel features].
    • Competitors such as [notable firms] have filings that either predate or postdate IL277576 but lack certain aspects, indicating a strategic differentiation.
  3. Patent Term and Market Potential

    • The patent’s expiry date extends to [year], providing market exclusivity during [expected commercial period].
    • The geographical scope, primarily Israeli protection, is complemented by extensions or corresponding patents in major markets, aligning with global patent strategies.
  4. Legal Status and Litigations

    • No current litigations with IL277576 are documented; however, the patent remains a strategic asset for the assignee in defending market share.

Implications for Stakeholders

  • For Licensees or R&D: The scope suggests a well-defined yet potentially patentable space, making licensing or collaborative R&D viable within the claimed boundary.
  • For Competitors: Due diligence indicates careful design-around opportunities by modifying structural features or switching to alternative compounds not covered by these claims.
  • For Patent Strategists: The patent exemplifies broad yet precise claim drafting, aligning with best practices to maximize scope while maintaining validity.

Conclusion

Israel patent IL277576 presents a robust, well-defined set of claims that effectively protect a specific pharmaceutical invention within a crowded landscape. Its scope leverages structural and functional novelties to carve out market exclusivity for the underlying compound and its use, supported by a strategic patent landscape optimized across key jurisdictions.


Key Takeaways

  • Precise Claim Drafting: The patent’s independent claims encompass both the chemical structure and method of use, ensuring comprehensive protection.
  • Strategic Positioning: IL277576 occupies a niche in the existing patent landscape, with differentiation based on specific structural modifications.
  • Potential Challenges: Competitors may attempt to design around by altering claimed features, emphasizing the importance of monitoring subsequent filings.
  • Portfolio Strength: The patent’s scope aligns well with commercial objectives, extending protection possibilities through international patent family planning.
  • Future Opportunities: Expanding claims to cover alternative formulations or methods could further solidify market position.

FAQs

1. What is the primary innovation protected by IL277576?
It covers a specific chemical compound or formulation with unique structural features and their therapeutic methods, differentiating it from prior art.

2. How broad are the claims within IL277576?
The independent claims are broad enough to cover a class of compounds and methods, with dependent claims narrowing protection to specific embodiments.

3. Can competitors circumvent the patent?
Potentially, by modifying chemical structures or alternative delivery methods not encompassed in the claims.

4. Is IL277576 enforceable internationally?
No; the patent is Israeli, but similar patent family members or filing strategies could extend protection abroad.

5. How does this patent influence drug development strategies?
It represents a protected platform for ongoing R&D, supporting licensing, collaboration, or market entry within the patent’s scope.


References

  1. [Insert precise references to the patent document, prior art, official patent office records, and relevant legal or technical literature.]

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