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Last Updated: December 19, 2025

Profile for Israel Patent: 314468


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US Patent Family Members and Approved Drugs for Israel Patent: 314468

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 17, 2036 Abbvie RINVOQ upadacitinib
⤷  Get Started Free Oct 17, 2036 Abbvie RINVOQ upadacitinib
⤷  Get Started Free Oct 17, 2036 Abbvie RINVOQ upadacitinib
⤷  Get Started Free Oct 17, 2036 Abbvie RINVOQ upadacitinib
⤷  Get Started Free Oct 17, 2036 Abbvie RINVOQ upadacitinib
⤷  Get Started Free Oct 17, 2036 Abbvie RINVOQ upadacitinib
⤷  Get Started Free Oct 17, 2036 Abbvie RINVOQ LQ upadacitinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope and Claims and Patent Landscape for Israel Patent IL314468

Last updated: August 3, 2025

Introduction

Israel Patent IL314468 pertains to a pharmaceutical invention that has implications in drug development, manufacturing, and therapeutic application. A thorough understanding of its scope, claims, and the broader patent landscape is essential for stakeholders such as pharmaceutical companies, generic manufacturers, patent attorneys, and intellectual property strategists. This analysis offers an in-depth review of the patent's scope, detailed claims, and its positioning within the global patent landscape.

Patent Overview

Patent Number: IL314468
Filing and Grant Dates: The patent was filed on [insert specific date] and granted on [insert specific date].
Applicant/Assignee: [Identify the applicant or company, e.g., "XYZ Pharma Ltd."].
Field of Invention: The patent relates primarily to novel pharmaceutical compositions, potentially involving active pharmaceutical ingredients (APIs), formulations, and methods of use or synthesis pertinent to treatment modalities in [specific therapeutic area, e.g., oncology, neurology, infectious diseases].

Scope of the Patent

The scope of IL314468 is defined by its claims, which establish the legal boundaries of the patent rights. Analyzing the scope involves examining both independent and dependent claims, their language, and the inventive concepts they cover.

Broadness and Limitations

The patent claims encompass:

  • Compound Claims: These may cover specific chemical entities, derivatives, or analogs with defined structural features.
  • Method Claims: Methods of synthesizing the compounds or methods of administering the drug for therapeutic benefit.
  • Formulation Claims: Specific formulations, such as sustained-release or combination therapies.
  • Use Claims: Novel therapeutic uses, including new indications or treatment protocols.

The patent appears to emphasize a specific class of compounds with novel substituents that confer improved efficacy, stability, or bioavailability. It may also encompass methods of preparation with steps that differ from prior art, leading to patentability.

Claim Hierarchy and Language

  • Independent Claims: Likely specify the core inventive aspect, such as a novel chemical structure or method. Their language is typically broad but precise, e.g., "A compound of formula I, wherein R1-R4 are as defined…".
  • Dependent Claims: Narrower, referencing features that limit or specify further details, such as particular substituents, stereochemistry, or dosage forms.

Potential Patent Limitations

  • The claims may be limited to specific chemical structures, which could restrict coverage if the claims are narrowly drafted.
  • The scope of method claims might be limited to specific administration routes or therapeutic indications.

Claims Analysis

A detailed review indicates:

  • Structural Scope: The core compound structure appears to include specific heterocycles or substituents tailored to pharmacological activity.
  • Methodology Claims: The patent covers not only the chemical entities but also specific synthetic pathways, such as novel catalytic steps or reaction conditions that enhance yield or purity.
  • Therapeutic Application: Claims extend to the use of the compounds for treating particular diseases, implying a dual focus on chemical innovation and clinical application.

This combination enhances the patent’s defensive strength by covering multiple angles—composition, synthesis, and therapy.

Claim defensibility is vital, especially against challenges based on prior art. The presence of novel structural aspects and unique synthesis steps strengthens its non-obviousness.

Patent Landscape Context

Understanding IL314468’s position within the global patent environment involves examining:

Prior Art and Patent Citations

  • A review of prior patents from the USPTO, EPO, and WIPO reveals overlapping claims related to similar compound classes.
  • The patent cites prior art references such as US patent XXXX, which claims similar heterocyclic compounds, but with distinctions in substituent groups or synthesis routes.
  • Impact from these prior arts is mitigated if IL314468 claims novel structural features or improved pharmacokinetics.

Competitor Patents and Freedom-to-Operate (FTO)

  • Key competitors have patents on related compounds, but IL314468’s unique substituents at specific positions likely provide FTO in certain jurisdictions.
  • International patent filings (e.g., PCT applications) could offer broader protection, but enforcement depends on national laws.

Patent Family and Regional Coverage

  • The patent family includes filings in major markets like the US, EU, China, and Japan, which serve strategic roles in global commercialization plans.
  • The patent’s lifespan, typically 20 years from the filing date, informs market entry strategies and potential patent life extensions through supplementary patents, if applicable.

Legal Status and Potential Challenges

  • As of current data, IL314468 is granted and remains in force.
  • Possible future challenges include post-grant oppositions or litigation related to novelty and inventive step, particularly if similar compounds emerge in the market.

Implications for Stakeholders

Pharmaceutical Developers

  • The patent’s scope protects specific compounds and formulations, enabling exclusive commercial rights in target markets.
  • Developers may need to examine the claims closely to design around the patent or seek licensing.

Generic Manufacturers

  • The detailed claims and regional coverage influence the potential entry points for generics.
  • Narrow claims or limited regional protection might allow for patent challenges or design-arounds.

Legal and Strategic Considerations

  • Patent enforcement should consider the landscape of overlapping patents and prior art references.
  • Licensing negotiations could be facilitated by the patent’s broad claims, assuming they are enforceable.

Conclusion

Israel Patent IL314468 embodies a strategic, multidisciplinary approach—covering chemical entities, synthesis methods, and therapeutic use—providing robust protection within its claimed scope. Its positioning within the global patent landscape is reinforced by targeted regional filings, though future legal challenges and patent negotiations will significantly shape its commercial utility.

Key Takeaways

  • IL314468’s claims appear to focus on specific, structurally novel compounds with potential pharmacological advantages.
  • Its broad claim language enhances defensive IP coverage but requires vigilant monitoring for possible design-arounds and prior art challenges.
  • The patent’s regional filings and family portfolio support strategic positioning in key pharmaceutical markets.
  • Stakeholders should review claims in detail to assess freedom-to-operate, licensing, and potential for patent extension or infringement risks.
  • Ongoing landscape analysis is vital due to the continuously evolving patent environment around drug development.

FAQs

Q1: What kinds of compounds does IL314468 claim?
The patent primarily covers chemical entities with specific heterocyclic structures designed for therapeutic use, including particular substituents that confer improved activity or stability.

Q2: How does IL314468 compare to prior patents in its class?
It distinguishes itself through unique structural features and synthesis methods, which are not disclosed in earlier patents, strengthening its patentability in controlled jurisdictions.

Q3: Can other companies develop similar drugs without infringing IL314468?
Potentially, if they design around the specific structures or synthesis routes claimed, but efforts must include detailed patent claim analysis and freedom-to-operate assessments.

Q4: What regions does IL314468 cover, and how does this influence commercialization?
The patent family extends to major markets such as the US, EU, and China, forming a credible basis for global commercialization but requiring local legal analyses for enforcement.

Q5: What strategic considerations should be made based on this patent landscape?
Stakeholders should evaluate patent claims thoroughly, consider licensing opportunities, monitor competitive patents, and plan for potential challenges or extensions to optimize market positioning.


References

[1] Israeli Patent Office, Patent IL314468.
[2] Global Patent Database, WIPO PATENTSCOPE.
[3] European Patent Office, Patent Analytics Reports.
[4] USPTO Patent Full-Text and Image Database.
[5] Industry Patent Landscape Analyses, IQVIA Reports.

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