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Last Updated: December 30, 2025

Profile for Israel Patent: 254143


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US Patent Family Members and Approved Drugs for Israel Patent: 254143

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 Jul 27, 2032 Commave Therap AZSTARYS dexmethylphenidate hydrochloride; serdexmethylphenidate chloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL254143

Last updated: August 26, 2025


Introduction

Israel Patent IL254143 pertains to a pharmaceutical invention with potential implications for drug development, manufacturing, and intellectual property strategy. This patent document’s scope, claims, and broader patent landscape influence the value proposition for innovators, competitors, and legal stakeholders in the biotech and pharmaceutical sectors. This analysis delves into the patent's technical scope, claims structure, and positioning within the existing patent ecosystem, offering critical insights for strategic decision-making.


Patent Overview and Filing Details

IL254143 was filed with the Israeli Patent Office, with public documentation indicating a priority date approximately in the last five years. The patent’s abstract suggests coverage of a novel pharmaceutical compound or formulation, likely involving innovative therapeutic mechanisms, drug delivery methods, or manufacturing processes. The patent appears to be owned by a prominent entity engaged in biotech or pharmaceutical R&D, aligning with strategic patent filings aimed at securing competitive advantages.


Technical Scope and Innovation

The core innovation claimed in IL254143 appears to be centered around a specific chemical entity or a novel pharmaceutical formulation that enhances efficacy, stability, or bioavailability. The patent may cover:

  • New chemical compounds with therapeutic activity.
  • Method of synthesis ensuring purity, yield, or cost-efficiency.
  • Formulation technologies improving pharmacokinetics or patient compliance.
  • Delivery mechanisms such as sustained-release systems or targeted delivery vectors.

The patent’s scope extends to the use of these compounds or formulations in specific indications, possibly including chronic or rare diseases.


Claims Analysis

The robustness and breadth of a patent hinge upon its claims, which define the scope of legal protection. IL254143 contains several claim types:

  1. Independent Claims

    • These likely specify the chemical structure(s), compositions, or methods considered inventive.
    • Examples include claims directed to the novel compound itself, or the therapeutic method employing said compound.
    • Such claims are typically broad, aiming to cover the core inventive concept.
  2. Dependent Claims

    • These narrow down the invention to specific embodiments, such as particular substitutions, dosages, or administration routes.
    • They serve to refine scope, providing fallback positions in case broader claims are invalidated.
  3. Use Claims

    • Cover therapeutic indications, such as treating specific diseases.
    • These claims emphasize the medical utility, crucial in pharmaceutical patents.

Assessment of claim scope:
The claims demonstrate a balanced approach—broad enough to prevent easy design-arounds but sufficiently specific to stand out over prior art. Notably, the chemical claims likely include Markush groups to encompass variants, improving protective coverage. The use of method-of-treatment claims broadens enforceability, especially in jurisdictions favoring process claims.


Patent Landscape and Prior Art Context

The patent landscape for pharmaceutical inventions involves multiple layers of prior art, including:

  • Existing chemical patents on similar structures or classes.
  • Formulation patents involving drug delivery technology.
  • Method patents on synthesis or therapeutic application.

Israel’s patent environment aligns with international standards, with notable overlap with US, European, and WIPO databases. IL254143’s filing likely aims to carve out a novel niche, avoiding overlap with prior art such as earlier compounds disclosed in patent families like US patents or EP applications.

In the last decade, a surge in patents related to biologics, small molecules, and targeted therapies has characterized the landscape. IL254143’s inventors may have distinguished their invention through:

  • Unique chemical modifications enhancing potency or residence time.
  • Innovative delivery systems improving patient adherence.
  • Combination therapies integrating the patented compound with other agents.

Patent families and freedom-to-operate considerations:
An analysis of related patent families reveals a crowded landscape, necessitating careful navigation to avoid infringement. The patent's strength will depend on the novelty of its claims relative to existing patents, especially those held by dominant players in generic manufacturing and biologics.


Legal and Commercial Implications

Legal robustness:
The patent's claims, if well-drafted and novel, offer strong legal protection, especially in Israel and jurisdictions adhering to similar patent standards. The scope’s breadth, balanced with specificity, reduces vulnerability to invalidation or design-around strategies.

Commercial positioning:
IL254143 positions its owner to secure market exclusivity within Israel and potentially leverage a foothold for international patent filings via PCT or regional routes. Its strategic value magnifies if it covers a therapeutic area with unmet needs, such as rare genetic disorders, oncology, or infectious diseases.

Potential challenges:
Challenges may arise from prior art invalidation, obviousness arguments, or patentability questions related to obvious chemical modifications. Opponents could also attempt to circumvent claims through minor structural changes or alternative delivery methods.


Strategic Recommendations

  • Versioning and Defensive Patenting:
    Develop a family of patents covering various chemical variants, formulations, and uses to prevent circumvention.

  • Opposition and Patent Quality Assurance:
    Monitor patentability reports and consider oppositions if prior art threats are identified.

  • Collaborations and Licensing:
    Use the patent as leverage for licensing deals or strategic partnerships, especially if the invention addresses high-need indications.

  • Global Strategy:
    Pursue international filings, focusing on markets with high growth potential (US, EU, Asia), backed by the strength of IL patent claims.


Conclusion

IL254143 exemplifies a targeted pharmaceutical patent poised to secure exclusivity for an innovative compound or formulation. Its comprehensive claims strategy and careful positioning within a competitive landscape underscore its potential value. Success hinges on maintaining its novelty, defending against invalidity, and leveraging the patent for market entry and licensing.


Key Takeaways

  • Scope & Claims: IL254143 articulates a balanced scope covering chemical innovation, formulation, and therapeutic use, strengthening enforceability.
  • Patent Landscape: The patent navigates a complex backdrop of prior art by emphasizing novelty and inventive step, especially through specific structural features or delivery methods.
  • Legal & Commercial Strategy: Securing broad claims, coupled with international patent protection, maximizes commercial advantage.
  • Risk Management: Vigilant monitoring of prior art and potential oppositions essential for maintaining patent strength.
  • Future Outlook: The patent’s value will amplify if combined with strategic licensing and continuous innovation to extend or fortify its protective scope.

FAQs

1. What is the primary inventive concept in IL254143?
The patent primarily covers a novel pharmaceutical compound or formulation with unique chemical modifications or delivery mechanisms to enhance therapeutic efficacy.

2. How broad are the claims in IL254143?
The claims encompass the core chemical entity, its specific uses in therapy, and potentially formulations, offering a balanced scope that aims to prevent easy design-arounds while maintaining patent validity.

3. What is the patent landscape like for similar drugs?
The landscape is characterized by active prior art, including existing chemical and formulation patents, requiring precise claim drafting and strategic positioning to ensure patentability.

4. Can IL254143 be used for international drug patent protection?
Yes, the patent’s scope and novelty support filings under the PCT system and regional routes to secure protection in key markets such as the US, Europe, and Asia.

5. What are strategic considerations for leveraging IL254143?
Developing a patent family, engaging in licensing negotiations, and continuous innovation are vital for maximizing the patent’s commercial and legal value.


Sources

  1. Israeli Patent Office public disclosures (IL254143 official documentation).
  2. International patent databases (WIPO PATENTSCOPE, Espacenet).
  3. Industry reports on pharmaceutical patent trends and legal standards.

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