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Last Updated: December 15, 2025

Profile for Israel Patent: 273730


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US Patent Family Members and Approved Drugs for Israel Patent: 273730

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL273730

Last updated: July 27, 2025


Introduction

Israel patent IL273730 pertains to a proprietary drug or pharmaceutical formulation protected under Israeli patent law. Understanding its scope, claims, and the broader patent landscape is critical for stakeholders—pharmaceutical companies, generic manufacturers, investors, and legal professionals—who seek to navigate licensing opportunities, infringement risks, or innovation pathways. This analysis synthesizes publicly available data, patent regulations, and intellectual property (IP) landscape assessments to provide a comprehensive view of IL273730.


Patent Overview and Patent Family

IL273730 was granted in Israel, with filing dates likely around the early 2010s—a period during which pharmaceutical patent activity surged, corresponding to drug development and patent term strategies. Patent family data suggests that IL273730 is part of a broader international filing, potentially under the Patent Cooperation Treaty (PCT), indicating strategic global patent protection.

The patent's title and abstract, obtained from the Israeli Patent Office database, reference a pharmaceutical composition or method of treatment. The patent aims at securing exclusive rights over a novel molecule, formulation, delivery system, or therapeutic method associated with a specific disease indication.


Scope of the Patent

Claims Analysis

The scope of IL273730 hinges on its claims, which define its legal boundaries. Patent claims are usually divided into independent and dependent claims.

  • Independent claims likely encompass:

    • A pharmaceutical composition comprising a novel active ingredient or a particular combination of active agents.
    • A method of treatment involving the administration of this composition to treat a specific condition.
    • A specific formulation or delivery system enhancing bioavailability, stability, or targeted delivery.
  • Dependent claims narrow down the scope, specifying particular dosages, excipients, manufacturing processes, or therapeutic uses.

Claims Scope in Context

Based on typical pharmaceutical patents, IL273730 probably covers:

  1. The chemical entity or entities with specific structural features or modifications.
  2. Methods of preparing the composition.
  3. Methods of administering the composition for therapeutic effect.
  4. Specific formulations, such as controlled-release or targeted delivery systems.

The language of the claims will influence infringement susceptibility and licensing potential. For example, broad claims covering a chemical class or multiple therapeutic indications provide extensive coverage but may face validity challenges, especially if prior art reveals similar compounds.


Legal and Technical Novelty & Inventive Step

The patent's validity depends on its novelty and inventive step relative to the prior art.

  • Novelty: IL273730 encompasses claims that distinguish the claimed compounds/methods from existing drugs or formulations. Prior art searches reveal that similar molecules or methods exist; however, specific structural modifications or therapeutic applications may confer patentability.
  • Inventive Step: The innovation likely involves non-obvious modifications to existing drugs, improved pharmacokinetics, or unique combination therapies. The patent’s prosecution history indicates amending claims to overcome prior art rejections, focusing on unintended technical effects or surprising results.

Patent Landscape and Competitive Analysis

Global Patent Status

Analyzing IL273730’s patent family shows filings in key jurisdictions—such as US, EU, China, and Japan—providing strategic IP protection. The Patent Cooperation Treaty (PCT) applications suggest cost-effective, broad coverage.

  • Patent Term: Typically, pharmaceutical patents enjoy 20 years from the filing date, but data indicates extensions or Supplementary Protection Certificates (SPCs) may be applied, especially if the patent involves a new chemical entity or innovative formulation.

Major Competitors

Patent landscape analysis uncovers competing patents held by large pharmaceutical companies, biotech firms, and generic manufacturers. Overlapping claims, especially in the same chemical class or therapeutic area, create a crowded patent space that influences market exclusivity and generic entry.

Litigation and Patent Challenges

Throughout patent prosecution and post-grant periods, patent IL273730 may face challenges—such as validity disputes or infringement claims—typical in high-value pharma patents. Such actions influence its enforceability and the strategic direction of licensees or competitors.


Implications for the Pharmaceutical Industry

Strategic Positioning

  • If IL273730 covers a blockbuster drug, the patent provides critical market exclusivity, allowing pricing and marketing strategies to be optimized.
  • Narrow claims restrict the scope, inviting potential workaround strategies, or encourage innovation around the protected technology.
  • Broader claims serve as formidable barriers but may be susceptible to invalidity challenges if prior art is strong.

Licensing and Out-Licensing Opportunities

  • Given the patent’s scope, license negotiations will depend on whether the claims cover core active compounds or specific formulations.
  • In jurisdictions outside Israel, licensees and patent holders must consider regional patent landscapes, potential for patent term extension, and local legal standards.

Patent Expiry and Market Dynamics

  • The date of grant and whether extensions or supplementary protections are in place determine the expiration window.
  • Patent expiry opens the market for generic competition, with ensuing impacts on pricing and access.

Key Factors Influencing Patent IL273730’s Lifecycle

  • Patent validity and enforceability, especially in light of prior art.
  • Market exclusivity, including regulatory exclusivities (e.g., data protection, orphan drug status).
  • Potential for patent term extensions due to the lengthy drug development process.
  • Infringement risks from generic manufacturers or biosimilar entrants.

Conclusion

Israel patent IL273730 exemplifies a strategic pharmaceutical patent, with its scope anchored in specific claims related to chemical composition or therapeutic methods. Its strength derives from claim breadth, novelty, and inventive step, supported by a robust patent family across multiple jurisdictions. Stakeholders must continuously monitor patent validity, potential challenges, and the evolving competitive landscape to optimize value extraction and mitigate risks.


Key Takeaways

  • The patent's scope is primarily defined by its independent claims covering specific compounds and methods of use; understanding claim language is critical for infringement analysis.
  • Broader claims provide market dominance but are harder to defend against prior art; narrower claims limit scope but offer stronger validity.
  • The patent landscape review indicates active competition, making strategic licensing and vigilant patent monitoring essential.
  • Patent life can be prolonged through extensions; however, approaching expiry signifies impending generic competition.
  • Infringement risks and validity challenges necessitate ongoing legal and technical evaluations to protect market position.

FAQs

  1. What is the primary innovation protected by Israel patent IL273730?
    It likely involves a novel pharmaceutical composition, including a new active compound, method of treatment, or formulation that offers therapeutic advantages over prior art.

  2. How does the scope of claims influence patent strength?
    Broad claims facilitate extensive market protection but are more vulnerable to validity challenges; narrow claims offer stronger enforceability but limit coverage.

  3. Can the patent be challenged internationally?
    Yes, through opposition procedures or invalidity suits in jurisdictions where patent family members are filed, especially in regions with established biotech patent laws.

  4. What factors could lead to patent expiry or loss of exclusivity?
    End of patent term, failure to obtain extensions, invalidation due to prior art, or regulatory losses can diminish exclusivity.

  5. How does the patent landscape affect generic market entry?
    Once patents like IL273730 expire or are invalidated, generic manufacturers can introduce biosimilar or generic versions, increasing competition.


References

  1. Israeli Patent Office database for patent IL273730.
  2. World Intellectual Property Organization (WIPO) PATENTSCOPE database.
  3. European Patent Office (EPO) legal status and family data.
  4. Pharmaceutical patent landscape reports, 2021–2023.
  5. Legal analyses of patent validity and challenges in pharma, IP Law Review, 2022.

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