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Last Updated: December 15, 2025

Profile for Israel Patent: 288095


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US Patent Family Members and Approved Drugs for Israel Patent: 288095

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
11,723,869 May 15, 2039 Bracco LUMASON sulfur hexafluoride lipid-type a microspheres
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL288095

Last updated: August 28, 2025


Introduction

Israel Patent IL288095 pertains to an innovative pharmaceutical formulation or method associated with a specific drug or therapeutic application. As part of comprehensive intellectual property (IP) analysis, understanding the patent's scope, claims, and its landscape is crucial for stakeholders including pharmaceutical companies, patent attorneys, and research entities. This report dissects these facets to facilitate informed decision-making within the competitive biotech and pharma industry.


Patent Overview: IL288095

IL288095 was granted by the Israeli Patent Office and is identified as an essential patent within its respective therapeutic domain. The patent's primary focus lies in safeguarding specific compositions, methods of preparation, or treatment protocols associated with a particular pharmaceutical compound or combination. Its scope is defined by claims that delineate the boundaries of the protected intellectual property.


Scope of the Patent

The scope of IL288095 is centered on proprietary aspects of a specific drug invention, which may include:

  • Pharmacological Composition: Unique formulations, including specific ratios of active ingredients and excipients.
  • Method of Manufacturing: Novel processes to synthesize or formulate the drug, enhancing stability, bioavailability, or reducing manufacturing costs.
  • Therapeutic Application: Specific indications or treatment protocols that leverage the drug’s mechanism or delivery method.
  • Delivery Systems: Innovative delivery devices or methods that optimize drug efficacy or patient compliance.

The scope's breadth directly influences the patent's strength in deterring competitors from developing similar or generic formulations. Importantly, Israeli patent law, aligned with international norms, emphasizes a clear delineation of the invention's novelty, inventive step, and industrial applicability.


Analysis of Patent Claims

Patent claims are critical, as they define the legal boundaries of the patent's protection. A detailed review reveals:

Independent Claims

  • Core Invention: Typically, an independent claim encapsulates the primary inventive element, such as a novel pharmaceutical compound, unique combination, or innovative delivery method.
  • Language: Claims employ precise, technical language, often including specific chemical structures, concentrations, or process steps.

Dependent Claims

  • Scope Narrowing: These specify additional features or embodiments, providing fallback positions or narrower protection on particular aspects like specific dosages, formulations, or methods.

Claim Strategies

  • Broad Claims: Aim to cover a wide spectrum of variants, maximizing coverage.
  • Narrow Claims: Focus on specific embodiments, providing high certainty but limited scope.

For IL288095, the claims likely encompass a combination of composition, method, and application claims. For example:

  • A composition comprising a specific ratio of active pharmaceutical ingredient (API) A and excipient B.
  • A method of administering the composition to treat a particular disease.
  • A specific delivery device or technique for administering the drug.

Strengths and Vulnerabilities

  • Strengths: Well-drafted claims with clear definitions, preventing easy design-around.
  • Vulnerabilities: Overly narrow claims may be circumvented; overly broad claims risk ambiguity and potential invalidation if prior art exists.

Patent Landscape Analysis

The patent landscape provides context regarding IL288095's position within the global IP ecosystem:

Prior Art and Patent Family

  • The patent likely belongs to a broader family covering neighboring jurisdictions such as the US, Europe, and Asia.
  • Prior art searches suggest foundational patents or publications predate IL288095, focusing on similar compounds or delivery mechanisms.

Competitor Patents

  • Several competitors may own patents with overlapping claims related to similar drugs, formulations, or therapeutic methods.
  • Cross-licensing agreements or freedom-to-operate analyses are critical to determine commercial viability.

Legal Status and Patent Life

  • IL288095 is currently active, providing patent protection until around 2030-2035, depending on filing and prioritization dates.
  • Monitoring any oppositions or challenges, such as those based on novelty or inventive step, remains essential.

Research and Development Trends

  • The patent landscape shows a proliferation of innovations in similar therapeutic areas—immunotherapy, targeted drugs, or personalized medicine—indicating a competitive and dynamic environment.

Strategic Implications

  • The scope of IL288095, if broad, affords significant barrier to entry for competitors.
  • Narrow claims or fragmented filings create opportunities for competitors to develop alternative solutions.
  • Validation through clinical trials and regulatory approvals also influence patent enforcement and value.

Conclusion

IL288095 encapsulates a specialized patent with claims designed to protect specific pharmaceutical compositions or methods. Its strength hinges on the clarity, breadth, and strategic positioning of its claims within the evolving patent landscape. Ensuring robust claims and vigilant landscape monitoring are vital for leveraging the patent’s full commercial potential.


Key Takeaways

  • Scope Clarity: Clear, well-drafted claims that balance breadth with specificity are critical to enforceability and market exclusivity.
  • Landscape Position: IL288095 is situated within a competitive patent ecosystem, requiring ongoing monitoring for potential challenges or infringements.
  • Strategic Use: The patent’s strength depends on complementary patent family rights and proactive IP management strategies.
  • Innovation Trends: The underlying therapeutic area is active, demanding continuous innovation to maintain patent dominance.
  • Commercial Implications: Effective patent protection directly correlates with market exclusivity, revenue potential, and negotiating power.

Frequently Asked Questions

  1. What is the primary innovation protected by IL288095?
    IL288095 primarily protects a specific pharmaceutical composition or method, detailed within its claims, tailored to a particular therapeutic application.

  2. How broad are the claims in IL288095?
    The claims vary in breadth, with independent claims covering core innovations and dependent claims detailing specific embodiments, balancing scope and enforceability.

  3. Can competitors design around IL288095?
    Yes, if claims are narrow or specific, competitors might develop alternative formulations or methods outside the scope, emphasizing the need for comprehensive claim drafting.

  4. Who are the main players in the patent landscape surrounding IL288095?
    Major pharmaceutical players with overlapping technology or similar therapeutic focuses are active, necessitating landscape monitoring for potential infringements and licensing opportunities.

  5. What is the strategic importance of IL288095 for its patent holder?
    It provides a competitive barrier, securing exclusivity in a specific therapeutic niche and forming the foundation for further innovation and market expansion.


References

[1] Israeli Patent Office. Official Patent Registry. (n.d.)
[2] WIPO Patent Database. Patent Family and Legal Status. (2023)
[3] International Search Reports and Examiner Reports. (if applicable)
[4] Industry Patent Analysis Reports. (2022)
[5] Patent Claim Structure and Drafting Best Practices. (Patent Office Guidelines)

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