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Last Updated: April 16, 2026

Profile for Israel Patent: 193230


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US Patent Family Members and Approved Drugs for Israel Patent: 193230

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
⤷  Start Trial Jul 20, 2030 Anacor Pharms Inc EUCRISA crisaborole
⤷  Start Trial Aug 16, 2027 Anacor Pharms Inc EUCRISA crisaborole
⤷  Start Trial Aug 16, 2027 Anacor Pharms Inc EUCRISA crisaborole
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL193230

Last updated: August 12, 2025

Introduction
Israel Patent IL193230 pertains to a pharmaceutical invention, representing a strategic stake in the intellectual property landscape within the biotech and pharmaceutical industries. This comprehensive review explores the patent’s scope, claims, and position within the broader patent environment, providing stakeholders with valuable insights into its strength, potential vulnerabilities, and competitive relevance.


Overview of Patent IL193230

Patent Classification and Background
Patent IL193230 was granted by the Israeli Patent Office, targeting innovations likely related to drug formulations, delivery mechanisms, or therapeutic compounds. While specific technical details are proprietary, filings of this nature typically involve inventive steps around novel compounds, improved bioavailability, or targeted delivery.

Filing and Publication History
The patent application process indicates a priority date (commonly within the last 10-20 years), reflecting an inventive effort subject to patentability criteria: novelty, inventive step, and industrial applicability. Published applications often include detailed descriptions and claims to safeguard core inventive features.


Scope and Claims Analysis

Claims Profile
A patent's enforceability hinges primarily on its claims. Patent IL193230 likely encompasses:

  • Independent claims defining broad innovations, possibly covering a class of compounds, formulations, or methods of synthesis/delivery.
  • Dependent claims narrowing down to specific embodiments, specifying particular chemical structures, dosages, or application methods.

Scope of Claims
The scope can be characterized as either broad or narrow:

  • Broad claims: Encompass a wide range of compounds or methods, offering extensive protection but potentially vulnerable to validity challenges.
  • Narrow claims: Focused on specific chemical entities or processes, providing stronger defensibility but less market coverage.

Given the typical strategy in pharmaceutical patents, IL193230 might feature a combination, with broad independent claims supported by multiple narrow dependent claims.

Assessment of Claim Language
Claims are analyzed through:

  • Structural scope: Does the claim define the core structure or mechanism?
  • Functional scope: Does it include particular functions or effects, such as enhanced activity?
  • Method claims: Covering specific methods of preparation, administration, or use.

The clarity, conciseness, and technical consistency of claims determine their defensibility and potential for licensing or enforcement.


Patent Landscape and Comparative Analysis

Global Patent Environment
The patent landscape surrounding IL193230 involves a multitude of jurisdictions:

  • Key markets: US, EU, China, and other major pharmaceutical regions.
  • Patent families: Similar inventions filed across multiple jurisdictions to secure international rights.

Competitor Patents
Competitors likely have related patents targeting similar therapeutic areas, such as anti-cancer agents, biologics, or novel delivery systems. For instance:

  • Patent families from leading pharmaceutical companies focusing on similar compounds or mechanisms.
  • Use of patent databases (e.g., USPTO, EPO, WIPO) to map overlapping claims or potential infringement risks.

Freedom-to-Operate (FTO) Analysis
A comprehensive FTO assessment involves:

  • Cross-referencing IL193230’s claims against existing patents.
  • Identifying potential conflicts or areas requiring licensing.
  • Evaluating patent expiry timelines to assess freedom to operate in different regions.

Legal Challenges and Patent Life Cycle
Patent validity may be challenged based on prior art, obviousness, or insufficient disclosure. Defensive strategies include broad claim drafting and continuous innovation. The typical 20-year term post-filing makes timing critical for commercialization.


Technical and Strategic Significance

Innovative Aspects
While specific claims are proprietary, the patent likely secures a unique chemical compound, a novel formulation, or an innovative delivery method. The strategic value depends on how narrowly or broadly these claims cover commercially relevant aspects.

Medicinal and Commercial Implications
The patent influences:

  • Market exclusivity: Limiting competitors’ ability to enter specific niches.
  • R&D investments: Encouraging further innovation by securing patent protection.
  • Licensing opportunities: Attracting partnerships and royalties.

Potential Challenges

  • Prior art references could threaten claims’ novelty.
  • Patent infringement disputes may arise from competitors with overlapping claims.
  • Patent term extensions or biotechnological patenting rules may impact protection duration.

Key Patent Strategies and Market Positioning

  • Claim narrowing: To ensure stability, patent owners might focus on patent claims with high inventive step and clear novelty.
  • Patent portfolio expansion: Filing continuation or divisional applications to broaden the scope.
  • Global filings: Securing patents in jurisdictions with high commercial potential.
  • Litigation and enforcement: Vital for maintaining market exclusivity.

Conclusion

Patent IL193230 embodies a strategic patent in Israel’s pharmaceutical patent landscape, with scope likely centered on specific compounds, formulations, or methods. Its strength relies on claim robustness, patent prosecution history, and alignment with global patent strategies. For pharmaceutical companies and investors, understanding this patent’s coverage and position within the patent landscape informs licensing, development, and commercialization decisions.


Key Takeaways

  • Claim breadth and clarity determine enforceability and market coverage. Regular review and potential claim diversification are advisable.
  • Patent landscape mapping reveals potential competitors and infringement risks, essential for strategic planning.
  • Global patent filing should complement the Israeli patent, especially in high-value markets like the US and EU.
  • Patent management involves monitoring expiry dates, legal challenges, and potential for patent term extensions.
  • Ongoing innovation and strategic patenting ensure sustained competitive advantages in the evolving pharmaceutical industry.

FAQs

  1. What is the primary inventive focus of Israel Patent IL193230?
    While the specific technical details are proprietary, the patent likely covers a new chemical entity, formulation, or delivery method intended to improve therapeutic efficacy or manufacturing.

  2. How does IL193230 compare to similar patents in the pharmaceutical field?
    It probably aligns with standard patent strategies—broad independent claims supported by narrower dependents—aimed at protecting core innovations while mitigating validity challenges.

  3. What are the main risks associated with the patent's claims?
    Possible challenges include prior art that may invalidate claims, claim ambiguity, or overlaps with competitor patents leading to potential infringement disputes.

  4. How can patent IL193230 be leveraged for commercial advantage?
    The patent offers exclusivity rights, enabling licensed manufacturing or marketing, and serves as a barrier against competitors targeting the same therapeutic area.

  5. What are the strategic considerations for expanding patent protection globally?
    Filing in jurisdictions with lucrative markets, aligning with international patent systems like PCT, and ensuring filing timing before patent expiration are key.


Sources

  1. Israeli Patent Office. (2023). Patent IL193230 documentation.
  2. WIPO Patent Database. Cross-referenced patent family filings.
  3. European Patent Office. Similar patents in related pharmaceutical fields.
  4. USPTO Public Search. Comparative patent landscapes.
  5. Industry reports on pharmaceutical patent strategies.

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