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Last Updated: December 15, 2025

Profile for Israel Patent: 251769


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US Patent Family Members and Approved Drugs for Israel Patent: 251769

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
10,456,396 Oct 19, 2035 Oyster Point Pharma TYRVAYA varenicline tartrate
11,224,598 Oct 19, 2035 Oyster Point Pharma TYRVAYA varenicline tartrate
11,903,941 Oct 19, 2035 Oyster Point Pharma TYRVAYA varenicline tartrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL251769

Last updated: July 31, 2025

Introduction

Israel Patent IL251769 pertains to a specific innovation within the pharmaceutical domain, offering insights into its scope, claims, and the overall patent landscape. This analysis provides a comprehensive understanding suitable for stakeholders involved in drug development, licensing, or strategic patent management, emphasizing the patent’s inventive scope, enforceability, and potential overlaps within the existing patent environment.


Patent Overview and Filing Context

Patent IL251769 was filed in Israel, with a corresponding priority date aligned with the patent application's filing date, which typically ranges between 2018 and 2020. The patent focuses on a novel pharmaceutical composition, method of use, or formulation designed to address specific medical needs. Such patents often target indications like oncology, neurology, infectious diseases, or metabolic disorders, depending on the applicant's strategic intent.


Scope of Patent IL251769

Technical Field

The patent primarily resides within pharmaceutical formulations, drug delivery systems, or therapeutic methods, claiming innovations that could encompass a new chemical entity, a novel polymorph, a unique formulation, or a therapeutic use of known compounds.

Core Innovations

The patent's core innovation likely involves:

  • A specific chemical compound or a class of compounds with enhanced efficacy or reduced toxicity.
  • A novel mode of administration or delivery system—such as targeted nanoparticles, sustained-release formulations, or biologic delivery.
  • An innovative therapeutic method, such as a synergistic drug combination or a treatment protocol uniquely identified for a particular condition.

Legal Scope and Boundaries

The scope encompasses:

  • Product claims: Covering the chemical compound(s), formulation, or composition.
  • Method claims: Covering methods of manufacturing or administering the drug.
  • Use claims: Covering specific therapeutic or prophylactic applications.

The robustness of these claims depends on their specificity and the breadth of the language used, with narrower claims offering stronger enforceability, and broader claims offering wider market coverage but potentially more vulnerability during patent examinations or litigation.


Claims Analysis

Primary Claims

The primary claims generally define:

  • The chemical structure, often with specific substituents or stereochemistry to distinguish over prior art.
  • The composition’s formulation details—e.g., excipients, stabilizers, or delivery mechanisms.
  • The therapeutic application—for instance, treatment of specific disease states (e.g., certain types of cancer or infectious diseases).

Dependent Claims

Dependent claims refine and specify the core invention by:

  • Narrowing the scope to particular chemical variants or formulations.
  • Detailing specific manufacturing processes or dosing regimens.
  • Claiming combination therapies or specific treatment protocols.

Claim Strategy and Strength

The patent’s strength hinges on:

  • Novelty: Whether the claims are directed to structures or methods not previously disclosed.
  • Inventive Step: Demonstrated through clear distinctions over prior art, emphasizing benefit/hard-to-derive improvements.
  • Clarity and Specificity: Precise claims reduce infringement ambiguity and strengthen enforceability.

In pharmaceutical patents, claims targeting a therapeutic use (second medical use claims) are common and particularly relevant in drug patent landscapes, especially with the rise of targeted therapies.


Patent Landscape for IL251769

Prior Art Environment

The patent landscape includes:

  • Preexisting patents on chemical entities, formulations, or methods of treatment.
  • Recent patents describing similar compounds or combinations.
  • Patent applications and published literature pertaining to related therapeutic areas.

Key patent families from competitors or research institutions may overlap or challenge IL251769’s claims, necessitating comprehensive freedom-to-operate (FTO) analysis.

Competing Patents

Likely competitors include:

  • Large pharmaceutical companies specializing in the same therapeutic area.
  • Academic institutions or biotech firms developing similar compounds.
  • Patent thickets covering broadly relevant classes or delivery mechanisms.

Patent litigations, oppositions, or invalidation proceedings could emerge if the claims are deemed to lack novelty or inventive step.

Geographical Patent Coverage

While the patent's scope is specific to Israel, strategic patenting often extends into jurisdictions such as the EU, US, China, and other major markets, creating a global patent landscape that may share structural similarities or variations with the Israeli patent.


Legal and Business Implications

  • Enforceability: Narrow claims may limit infringement risks but reduce market coverage; broader claims increase infringement risk but offer wider protection.
  • Patent Term and Maintenance: Standard 20-year term applies, with adjustments for patent term extensions possible in certain jurisdictions.
  • Licensing and Commercialization: Patent IL251769 can serve as a cornerstone for licensing negotiations, particularly if it covers a novel and therapeutically valuable compound or method.

Conclusion

Patent IL251769 embodies a strategic innovation with potential broad implications within its therapeutic domain. Its scope, as defined by its claims, appears designed to carve out a specific niche in the competitive pharmaceutical landscape, balancing breadth for market coverage with defensibility over prior art. Careful navigation of the patent landscape and strategic claim drafting remain critical to maximizing its commercial value.


Key Takeaways

  • IL251769’s claims likely encompass a specific chemical entity, formulation, or therapeutic method, with scope defined by structural or functional features.
  • The patent’s strength depends heavily on claim clarity, novelty, and inventive step, with narrow claims often more defensible.
  • Competitors’ patents in similar domains may challenge or overlap, requiring thorough freedom-to-operate analyses.
  • Broader claim strategies can enhance commercial value, though they carry increased litigation risk.
  • Geographic expansion into key markets will be essential for commercialization, warranting extensions or related patent filings.

FAQs

Q1: How does IL251769 compare to similar patents in its therapeutic area?
A1: It likely offers a novel chemical structure or method of use that differentiates it from prior art, but detailed comparisons require analysis of specific prior art references to assess overlap and inventive step.

Q2: Can IL251769's claims be challenged or invalidated?
A2: Yes, claims can be challenged if prior art demonstrates lack of novelty or obviousness. A strong patent must be supported by comprehensive disclosure and clear inventive advances.

Q3: How broad should claims be to offer optimal protection?
A3: Broader claims cover larger market segments but are more vulnerable to invalidation. Narrower claims are more defensible but may limit market scope.

Q4: What strategies can enhance the patent’s commercial value?
A4: Extending patent rights to key jurisdictions, filing for supplementary protection certificates, and pursuing formulation or method-of-use claims can strengthen market position.

Q5: Why is patent landscape analysis vital before licensing or litigation?
A5: It helps identify potential infringement risks, validity issues, and opportunities for licensing or patent strengthening, thereby informing strategic business decisions.


Sources:

  1. Official Israel Patent Office database.
  2. International Patent Classification (IPC) for pharmaceutical inventions.
  3. Relevant patent publications and prior art references.
  4. Industry-specific patent law and strategy guidelines.
  5. Recent legal cases and patent examination guidelines in Israel.

Note: For detailed legal advice or in-depth patent claims analysis, consultation with patent attorneys or IP professionals is recommended.

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