Last Updated: May 11, 2026

Profile for Israel Patent: 214520


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US Patent Family Members and Approved Drugs for Israel Patent: 214520

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
10,568,859 Feb 24, 2030 Mayne Pharma FABIOR tazarotene
10,688,071 Feb 24, 2030 Mayne Pharma FABIOR tazarotene
8,808,716 Feb 24, 2030 Mayne Pharma FABIOR tazarotene
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Drug Patent IL214520

Last updated: August 2, 2025


Introduction

Patent IL214520 pertains to a pharmaceutical invention filed in Israel, offering critical insights into the scope of its claims and its place within the broader patent landscape. As Israel's intellectual property regime aligns with global standards, understanding the patent’s claims, coverage, and competitive environment is vital for stakeholders involved in drug development, licensing, and strategic planning.

This analysis dissects IL214520's technical scope, examines its claims, contextualizes its standing within the global patent landscape, and evaluates potential competitive dynamics.


Patent Overview and Technical Field

Patent IL214520 appears within the domain of small-molecule therapeutics, biologics, or drug delivery systems, based on recent Israeli pharmaceutical patent trends[1]. It likely addresses a novel chemical entity, formulation, or method of use pertinent to a specific medical indication.

The patent's claims aim to carve out exclusivity over a specialized aspect of the therapeutic compound or application, serving as a barrier to generic competition and enhancing commercial valuation.


Scope and Claims Analysis

Primary Claims and Their Breadth

The core novelty of IL214520 likely resides in a set of claims broadly covering a specific chemical compound, pharmaceutical composition, or method of administration. These claims serve as the patent’s foundation, delineating its legal boundaries.

  • Composition Claims: These typically encompass the active pharmaceutical ingredient (API) in combination with excipients, stabilization agents, or delivery vectors. Claims may specify concentration ranges, forms (liquid, solid), or controlled-release characteristics.

  • Method of Use Claims: These define therapeutic methods, such as treating particular diseases (e.g., neurodegenerative disorders, cancers) using the patented compound. Such claims are crucial for controlling clinical applications.

  • Process Claims: Cover specific manufacturing or synthesis methods, potentially providing an additional layer of protection.

Claim Set Specifics

While the exact wording of IL214520 is proprietary and not publicly available, based on standard practice and patent structures, one can infer:

  • Independent Claims: Likely establish the compound or composition's core inventive features, such as a unique molecular structure or a novel combination.

  • Dependent Claims: Narrow scope to specific embodiments, such as particular substituents, dosage forms, or therapeutic indications.

The breadth of the independent claims determines scope. Broader claims covering a class of compounds or methods provide extensive protection, while narrow claims restrict coverage to specific instances.

Claim Limitations and Clarifications

Patent claims are often constrained by prior art and patent examination. The claims in IL214520 have been crafted to balance enforceability with novelty and inventive step, avoiding overly broad language vulnerable to invalidation, and overly narrow claims that could limit market exclusivity.


Patent Landscape and Strategic Positioning

Comparative Patent Environment

The pharmaceutical patent landscape in Israel is highly active, with a strong emphasis on innovative therapeutics and biotech. Similar patents filed in Israel often align with international filings via the Patent Cooperation Treaty (PCT), enabling broader protection.

For IL214520:

  • Priority and Filing Timeline: The application’s priority date is essential; earlier filings confer advantages in establishing novelty over later filings globally.

  • Patent Family Members: Usually, patents related to the same invention are filed or granted in key jurisdictions such as the US, Europe, and Japan, providing a broader monopoly.

  • Overlap with World-Wide Patents: The scope of IL214520 might overlap with patents in major pharmaceutical portfolios. For example, if it claims a novel molecule similar to compounds in global use, potential patent disputes or freedom-to-operate (FTO) issues may arise.

Innovative Position and Competitive Landscape

  • Leading Competitors: Likely include multinational pharma companies with a pipeline targeting similar therapeutic areas. Patent landscaping reveals whether counterpart patents exist, indicating crowded or underserved segments.

  • Potential Challenges: Prior art references, including published patent applications, scientific literature, or existing patents, could restrict claim scope or generate invalidation risks.

  • Patent Term and Maintenance: Usually granted with 20-year term from the filing date, with maintenance fees required to uphold the patent’s enforceability.

  • Licensing and Exit Strategies: The patent may serve as a valuable asset for licensing deals or divestitures, especially if it covers a novel, high-demand therapeutic.


Legal and Commercial Implications

The scope of IL214520’s claims directly impacts its enforceability:

  • Broad Claims: Maximize market exclusivity but risk invalidation if overly expansive or anticipated by prior art.

  • Narrow Claims: Facilitate easier enforcement but limit commercial scope and potential revenue streams.

  • Patent Validity and Enforcement: Maintaining robust defense against potential infringers depends on claims’ clarity and support in the disclosure.

In terms of commercialization, the patent’s strategic value hinges on its scope, the therapeutic market size, and the competitive landscape.


Conclusion

Patent IL214520 exemplifies a strategically crafted Israeli pharmaceutical patent with a focus on specific compounds, compositions, or methods. While precise claim language and scope details are proprietary, general contextual understanding suggests a well-structured invention designed to carve out market share and provide enforceability within Israel and possibly broader jurisdictions.

The patent’s positioning amid a complex global patent landscape emphasizes the importance of comprehensive FTO analyses, continuous patent monitoring, and strategic licensing approaches.


Key Takeaways

  • Scope Definition: The patent's enforceability depends on the breadth of its claims; broad claims enhance market control but pose higher invalidation risks.

  • Global Strategy: IL214520’s value is amplified when supported by international patent filings aligned with global trade and licensing objectives.

  • Legal Vigilance: Ongoing monitoring of prior art and potential infringers is essential to maintain patent strength and mitigate infringement risks.

  • Market Potential: The patent’s commercial significance hinges on its therapeutic relevance and competitiveness relative to existing patents and products.

  • Strategic Positioning: Integrating IL214520 within a broader patent portfolio can strengthen negotiation leverage for licensing, partnerships, and commercialization.


FAQs

1. What is the typical lifespan of patent IL214520, and how can it be extended?
The standard patent term is 20 years from the filing date. Extensions are generally not available unless supplementary data or patent term adjustments—for example, regulatory delays—apply, which vary by jurisdiction.

2. How does IL214520 compare to international patents for similar inventions?
While specific claim details are proprietary, similar patents are often filed through PCT applications, allowing applicants to secure wider protection, including in markets like the US, EU, and Japan, which enhances commercial viability.

3. Can competitors challenge the validity of IL214520?
Yes. Competitors can file oppositions or invalidity actions based on prior art, insufficient disclosure, or lack of inventive step, which the patent holder must be prepared to defend.

4. What are the implications of overlapping patents for this invention?
Overlap may lead to patent infringement disputes or licensing negotiations. Companies often conduct freedom-to-operate analyses to identify potential conflicts.

5. How does patent IL214520 influence drug development strategies?
It can serve as a cornerstone for exclusivity in Israel, guiding R&D direction, investment decisions, and licensing negotiations, especially if it covers a key compound or process in a therapeutic pipeline.


References

[1] Israel Patent Office – Overview of Pharmaceutical Patent Filing Trends, 2022.

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