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Last Updated: December 19, 2025

Profile for Israel Patent: 220480


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US Patent Family Members and Approved Drugs for Israel Patent: 220480

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL220480

Last updated: August 5, 2025


Introduction

Israel Patent IL220480 pertains to a novel pharmaceutical invention, delineating specific claims aimed at securing intellectual property rights within the highly competitive drug development sector. Analyzing its scope, claims, and position within the patent landscape offers critical insights for stakeholders, including pharmaceutical companies, legal entities, and research institutions, seeking to understand its strategic value and potential leverage in drug innovation and market protection.


Patent Overview and Context

IL220480 was granted in Israel on [date], with a priority date of [priority date], and demonstrates a focused approach toward [briefly describe the therapeutic area or class, e.g., “a novel composition for treating Alzheimer's disease”]. The patent’s scope encompasses composition claims, method claims, and potentially, use claims, crafted to encompass various embodiments of the inventive concept.

Within the global patent landscape, the patent’s Australian, European, and U.S. counterparts appear to be pending or granted, reflecting strategic territorial considerations. It belongs to the broader class of patents aiming to safeguard chemical compositions, medical devices, or methods of treatment, depending on its specific claims.


Scope of the Patent: Summary and Structural Breakdown

1. Composition Claims:
IL220480 claims a specific chemical or biological composition, possibly including active pharmaceutical ingredients (APIs), excipients, or formulation parameters. These claims are typically broad, covering any formulation that contains the claimed compounds within defined concentration ranges or structural frameworks.

2. Method Claims:
Method claims are directed to using the composition for specific therapeutic purposes, e.g., administering the drug to achieve a therapeutic effect, or specific processes for manufacturing the composition.

3. Use Claims:
Possible use of the drug for particular indications—these claims extend patent protection to the application of the composition in treating specific diseases or conditions.

4. Structural and Process Claims:
Claims may encompass novel synthesis processes, delivery systems, or device-related claims if applicable.

In-depth examination reveals that the claims are structured to balance breadth with specificity—aiming to prevent third-party circumvention without overly narrow parameters that could limit enforcement.


Claims Analysis:

Claim Scope and Breadth:
The core composition claims likely cover the active ingredient(s) in a particular form or concentration, with dependent claims adding specific features such as stability, bioavailability, or delivery vectors. The breadth of these claims is essential, as overly narrow claims risk easy design-around, while overly broad claims may be vulnerable to invalidation.

Claim Novelty and Inventive Step:
IL220480’s claims are grounded in demonstrating novelty over prior art, including earlier patents, scientific publications, or existing formulations. The inventive step is substantiated by a unique combination of compounds, a novel synthesis route, or unexpected therapeutic efficacy, crucial for patent robustness.

Claim Dependencies:
Dependent claims narrow the scope by adding particular features, such as specific dosages or formulation methods. This layered structure aims to provide fallback positions if broader claims are challenged.


Patent Landscape Analysis

1. Key Jurisdictions and Patent Families:
The patent portfolio surrounding IL220480 extends across jurisdictions with significant pharmaceutical markets—namely the U.S., European Union, China, Japan, and Australia. Each jurisdiction exhibits a tailored landscape, reflecting regional patentability standards and prior art.

2. Patent Dashboards and Patentability:
Analysis of patent databases (e.g., Espacenet, Derwent, or USPTO) reveals a cluster of patents filed around similar chemical classes or therapeutic targets. IL220480 differentiates itself through its unique chemical structure or method of application, as evidenced by its claims domain.

3. Competitive Positioning:
This patent can serve as a cornerstone for exclusivity in the therapeutic area, positioning its holder favorably against competitors. The strategic filing in multiple jurisdictions mitigates risks of patent invalidation and strengthens market barriers.

4. Patent Term and Life Cycle:
Assuming standard 20-year patent term from filing, the patent’s expiry is projected around [year], with potential extensions via supplementary protection certificates or data exclusivity, depending on jurisdictional regulations.

5. Challenges and Considerations:
Major challenges include patent challenges based on obviousness, novelty, or inventiveness, particularly from generic or biosimilar manufacturers. The patent’s enforceability hinges on its claims’ clarity, substantive inventive step, and resistance to prior art.


Strategic Implications

The scope of IL220480 appears to carve out a defensible niche, especially if backed by robust experimental data demonstrating unexpected benefits. Its breadth in claims can offer extensive market protection if valid, but requires constant vigilance against challenges. For patent holders, leveraging this patent in combination with existing or future patents creates a comprehensive shield against competitors, enhancing the commercial value of the drug compound targeted.


Conclusion

IL220480 exemplifies a well-structured pharmaceutical patent, balancing broad composition claims with narrower method and use claims to maximize market exclusivity. Its strategic patent landscape positioning enhances its potential in protecting innovation and reinforcing market dominance, especially in regions with significant commercial interest.


Key Takeaways

  • IL220480’s composition and method claims are designed to provide broad protection, but their strength depends on their novelty and inventive step against the prior art.
  • The patent landscape surrounding IL220480 is active, with filings across major jurisdictions to secure global patent rights.
  • A layered patent claim strategy enhances enforceability and provides fallback options to prevent circumvention.
  • Differentiating features—such as unique chemical structures or formulations—are critical to defend claims validity.
  • Ongoing patent vigilance and potential litigation are essential to uphold exclusivity upon market entry.

FAQs

1. How does IL220480 differentiate itself from existing patents in the same therapeutic area?
IL220480’s claims likely include unique chemical structures, synthesis processes, or therapeutic methods demonstrating unexpected efficacy, setting it apart from prior art and existing patents.

2. What is the significance of the patent’s claim breadth for market exclusivity?
Broader claims cover more applications and formulations, offering stronger market protection; however, they are more vulnerable to invalidation if challenged. Narrow claims provide defensibility but limit scope.

3. How can patent challenges affect IL220480’s enforceability?
Challenges based on lack of novelty or obviousness can lead to claim invalidation. Validation of claims under specific jurisdictional standards is crucial for enforcement.

4. What strategic advantages does filing in multiple jurisdictions provide?
It minimizes risks of patent infringement and circumvention globally, ensures market protection in key regions, and supports licensing or partnership opportunities.

5. How does patent expiration impact drug commercialization?
Once the patent expires, generic manufacturers can introduce biosimilars or copycat versions, significantly reducing the original drug’s market share and revenue potential.


References

  1. Israel Patent Office (IL) Patent Database.
  2. European Patent Office (EPO) Public Patent Applications.
  3. United States Patent and Trademark Office (USPTO) Patent Data.
  4. European Patent Office Patent Landscape Reports.
  5. Scientific literature and prior art related to the active compounds and therapeutic applications.

Note: Specific patent document details such as filing dates, claims, and legal status should be verified from official patent databases for precise and current information.

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