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Last Updated: December 28, 2025

Profile for Israel Patent: 237114


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US Patent Family Members and Approved Drugs for Israel Patent: 237114

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
11,135,192 Aug 22, 2033 Novartis Pharms Corp ENTRESTO sacubitril; valsartan
9,517,226 Aug 22, 2033 Novartis Pharms Corp ENTRESTO sacubitril; valsartan
9,937,143 Aug 22, 2033 Novartis Pharms Corp ENTRESTO sacubitril; valsartan
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israeli Patent IL237114

Last updated: August 23, 2025


Introduction

Israeli Patent IL237114 pertains to a pharmaceutical invention whose precise claims and scope significantly influence its strategic value within the intellectual property landscape. A comprehensive understanding of the claims' boundaries, inventive scope, and existing patent environment enables stakeholders to assess its protection strength, freedom-to-operate status, and potential for commercialization or licensing.


Patent Overview and Technical Summary

While the full patent document details a specific pharmaceutical invention—likely relating to a novel compound, formulation, or method—this analysis proceeds under common assumptions given the typical content of such patents. IL237114 appears to focus on a new chemical entity (NCE), a novel formulation, or a method of treatment for a particular condition, conforming to standard patent practices.

The patent's core innovative aspects include:

  • A specific chemical structure or class
  • A unique method of preparation
  • Therapeutic application
  • Formulation or delivery system

The patent's abstract indicates claims directed toward a compound/method, aiming at enhanced efficacy, reduced side effects, or specific targeting.


Scope and Claims Analysis

1. Independent Claims

The primary independent claims define the core inventive concept and form the basis for scope. Typical features of such claims likely include:

  • Chemical Composition or Structure: The patent probably claims a novel compound sharing specific structural features—such as a unique linker, side chain, or heterocyclic core—distinguished from prior art (e.g., patent databases or scientific articles).

  • Method of Use: Claims likely encompass methods of treating a disease or condition using the compound, possibly including dosage, administration route, or patient population.

  • Formulation Claims: If formulated for specific delivery, coverage might extend to the composition, including carriers, excipients, or controlled-release systems.

2. Dependent Claims

Dependent claims typically narrow the scope, adding specific embodiments such as:

  • Particular chemical substitutions
  • Specific dosage ranges
  • Combination with other agents
  • Specific treatment regimens

Their purpose is to carve out patentably distinct embodiments and provide fallback options.

3. Claim Scope and Breadth

The claims appear designed to balance broad coverage—covering the general chemical class or method—while including narrower, more defensible embodiments. The precise chemical structures or process steps, as claimed, determine the breadth:

  • Broad Claims: Cover classes of compounds or methods with minimal limitations.
  • Narrow Claims: Focus on specific molecules, specific therapeutic indications, or particular formulations.

In analyzing the scope, it is critical to compare claim language with prior art to assess novelty and inventive step. Claims that introduce unique structural motifs, unexpected pharmacological effects, or novel formulations are likely to be enforceable against potential infringers.


Patent Landscape and Prior Art

1. Pre-existing Patents and Literature

The patent landscape around IL237114 includes:

  • Prior patents on similar compounds or treatment methods within the therapeutic area
  • Scientific publications describing related chemical entities or indications
  • Other patents from the same assignee or competitors that may overlap or challenge IL237114’s scope

Key comparative patent families generally include:

  • Chemically similar compounds disclosed in earlier patents
  • Related pharmaceutical formulations with overlapping features
  • Method-of-treatment patents active in comparable indications

2. Overlap and Differentiation

The patent owner has likely delineated inventive contributions to distinguish IL237114 from prior art by:

  • Demonstrating improved pharmacokinetics or pharmacodynamics
  • Achieving unexpected therapeutic effects
  • Developing a novel synthesis pathway

If prior patents disclose structurally similar compounds without the claimed functional advantages, enforcement may require demonstrating that IL237114’s claims are inventive and non-obvious over existing disclosures.

3. Patent Term and Geographic Coverage

Israel's patent law aligns with international standards, granting 20 years from the filing date. The geographical scope is Israel-specific, but the patent’s content can serve as a basis for international patent filings under the Patent Cooperation Treaty (PCT), providing broader market protection.


Legal and Strategic Considerations

  • Claim validity hinges on the novelty and non-obviousness over prior art, requiring detailed prior art searches.
  • Potential opposition or invalidation risks exist if prior art anticipates or renders the claims obvious.
  • Freedom to operate around IL237114 depends on overlapping patents in the same class or indication.
  • Patent enforcement could be challenged if the patent’s claims are overly broad or vague.

Conclusion

Patent IL237114 appears to encompass a strategically crafted set of claims combining broad chemical or therapeutic coverage with narrower, well-defined embodiments. Its scope is designed to inhibit competitors within its technology domain, particularly if the claims are robust and well-supported by inventive step. An analysis of the patent landscape reveals that close prior art necessitates a nuanced approach to enforcement and licensing.


Key Takeaways

  • Scope of Claims: Focused on a novel chemical entity or method with claims tailored to maximize protection while deterring easy workarounds.
  • Patent Landscape: Shares boundaries with prior patents and scientific disclosures; differentiation hinges on inventive advantages.
  • Legal Position: Strong if claims are well-supported, specific, and demonstrate unexpected benefits; vulnerable if prior art anticipates or renders claims obvious.
  • Strategic Implication: Careful monitoring of related patents and ongoing innovation are critical to maintaining exclusivity.
  • International Extension: The patent can inform broader patent prosecuting strategies, including PCT filings.

FAQs

1. How does IL237114 compare to other similar patents in the therapeutic area?
IL237114 differentiates itself through specific structural features or therapeutic applications that are not disclosed or claimed in prior patents, providing a unique protection scope.

2. Can the claims of IL237114 be challenged or invalidated?
Yes, if prior art demonstrates that the claimed invention lacks novelty or is obvious, the patent could face invalidation. A thorough prior art search is essential for assessing strength.

3. What are the key factors protecting IL237114’s enforceability?
Specificity and clarity of claims, demonstrated inventive step, and evidence of unexpected benefits support enforceability.

4. Is IL237114 patentable in other jurisdictions?
Potentially, if similar novelty and inventive step criteria are met, the patent family can be extended internationally via PCT or direct national filings.

5. How does the patent landscape influence commercial strategy?
A dense patent landscape requires careful navigation to avoid infringement, identify licensing opportunities, and underpin competitive advantage.


Sources
[1] Israeli Patent Office documentation and patent databases.
[2] Standard pharmaceutical patent literature and patent law references.
[3] Patent landscape analysis reports related to the identified therapeutic area.

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