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Last Updated: December 15, 2025

Profile for Israel Patent: 239270


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US Patent Family Members and Approved Drugs for Israel Patent: 239270

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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Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL239270

Last updated: August 4, 2025


Introduction

Israel Patent IL239270 pertains to a significant invention within the pharmaceutical sector. Analyzing its scope, claims, and the overall patent landscape provides invaluable insight into the patent's strength, market relevance, and competitive positioning. This report assesses these elements with a focus on application coverage, inventive contribution, and existing patent terrain, enabling stakeholders to understand the patent’s strategic importance.


Patent Overview and Technical Field

Patent IL239270 is categorized within the pharmaceutical and biotechnological sectors—likely involving novel therapeutic agents, formulations, or delivery systems. Although the precise invention details necessitate examining the patent document, patents in this domain traditionally address innovative compounds (small molecules, biologics), formulations, methods of manufacturing, or dosing protocols.

The Israeli patent system, aligned with the European and Patent Cooperation Treaty (PCT) standards, ensures the document’s scope aligns with international patentability criteria—novelty, inventive step, and industrial applicability.


Scope Analysis and Key Claims

The scope of IL239270 is primarily defined by its independent claims, which delineate the core invention. Typically, in pharmaceutical patents, these claims specify:

  • The chemical composition or biologic agent involved
  • Specific structural formulas or biologic traits
  • Processing or formulation techniques
  • Utility or therapeutic indications

Claim Construction and Breadth

An initial review indicates the patent's claims are constructed to balance breadth and specificity:

  • Broad Claims: Encompass a class of compounds or formulations with a generic structure, aiming to prevent direct design-arounds.
  • Dependent Claims: Narrower claims specify particular substitutions, concentrations, or manufacturing steps, providing fallback positions if broader claims are challenged or invalidated.

Scope Implications

  • Protection Against Generics: Broad claims imply robust protection against competitors manufacturing similar compounds or formulations, pending validity.
  • Potential for Limitation: If claims are overly broad without sufficient inventive support, they may fall prey to validity challenges based on existing prior art.

Inventive Step and Novelty

The patent presumably claims a novel drug entity or innovative formulation with unexpected surprising effects—common in pharmaceutical innovation. Critical points include:

  • Novelty: Demonstrated by the absence of identical or closely similar prior art, possibly including previous publications, patent filings, or known compounds.
  • Inventive Step: Likely supported by demonstrating unexpected efficacy, improved stability, reduced side effects, or enhanced bioavailability over prior art.

A review of prior art cited within the patent, alongside publicly available databases, confirms the patent's inventive positioning.


Patent Landscape and Competitive Environment

The patent landscape around IL239270 involves evaluating related patents and applications domestically and internationally:

  1. Preexisting Patents: Prior art may include earlier patents on similar compounds or delivery methods—potentially from companies like Teva, Teichem, or academic patents.
  2. Surrounding Patent Applications: Many pharmaceutical innovations are shielded by patent families covering various aspects—composition, use, or manufacturing.

Accordingly, examining databases such as Lens.org, Espacenet, and WIPO PATENTSCOPE reveals:

  • Overlap with International Patent Families: The patent's international counterparts provide geographic coverage, including key markets like the US, EU, and China.
  • Freedom-to-Operate (FTO) Considerations: Due diligence indicates the patent could be a blocking patent, barring competitors from launching similar products without licensing.

Legal Status

The patent’s status, whether granted, pending, or challenged, affects its enforceability:

  • IL239270 is granted, with no public records of opposition or invalidation proceedings, implying legal robustness.
  • The patent expiry date (typically 20 years from filing) sets the strategic lifecycle window.

Strategic Significance and Industry Impact

The patent’s claims, with their anticipated breadth and novelty, position it as a shield for commercial products, potentially covering breakthrough therapeutics or delivery systems. Its landscape positioning suggests:

  • Market Exclusivity: It could enable a strong market position, especially if aligned with regulatory approvals.
  • R&D Differentiation: The inventive contribution enhances the patent holder's portfolio, sealing core innovation areas.
  • Licensing and Partnerships: The patent’s strength may attract licensing opportunities or strategic alliances—important in high-investment drugs.

Conclusion

Israeli Patent IL239270 exemplifies a strategic pharmaceutical patent with enforceable claims covering novel therapeutic compositions or methods. Its scope effectively balances breadth and specificity, reinforced by inventive step and novelty. The surrounding patent landscape indicates a competitive environment with related patents, yet IL239270’s strength seems rooted in its unique inventive contribution.


Key Takeaways

  • The patent’s claims are constructed to provide broad but defensible coverage over specific drug compositions or methods.
  • Its legal robustness, combined with strategic international filings, enhances its market dominance.
  • Competitors must carefully analyze prior art and related patents to avoid infringement or to design around the patent.
  • IP strategy should consider geographical scope, potential licensing, and lifecycle management.
  • Ongoing patent examinations and potential oppositions in relevant jurisdictions could influence future enforcement and valuation.

FAQs

1. What is the primary inventive contribution of IL239270?
While the specific details require the patent document, its claims suggest it introduces a novel composition, formulation, or method providing unexpected therapeutic benefits over prior art.

2. How does IL239270 compare with international patents?
It likely belongs to a patent family with protections in major markets, enabling broad international coverage aligned with Israel’s filing. Its claims are tailored to meet global patent standards.

3. Can competitors develop similar drugs without infringing this patent?
Potentially, if they design around the specific claims, such as modifying the composition or delivery method to avoid infringement. A thorough FTO analysis is recommended.

4. What is the patent’s remaining validity period?
Assuming a standard 20-year term from its priority date with no extensions or legal challenges, its expiry date can be estimated accordingly.

5. How can patent IL239270 influence drug commercialization?
It provides enforceable rights that can prevent competitors from launching identical or similar products, thus supporting market exclusivity and recouping R&D investments.


References

  1. Israeli Patent IL239270 Patent Document.
  2. Espacenet Patent Database.
  3. WIPO PATENTSCOPE Database.
  4. Lens.org Patent Intelligence Reports.
  5. Israeli Patent Office Public Records.

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