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Last Updated: January 1, 2026

Profile for Israel Patent: 203171


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US Patent Family Members and Approved Drugs for Israel Patent: 203171

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
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL203171

Last updated: July 29, 2025

Introduction

Israel Patent IL203171 pertains to a novel pharmaceutical invention, whose scope and claims influence its legal protection, commercialization potential, and competitive landscape. This analysis examines the patent’s scope, core claims, their implications, and the broader patent landscape in Israel and globally. Such an understanding is pivotal for pharmaceutical companies, investors, and legal professionals seeking to navigate intellectual property rights effectively.

Patent Scope and Fundamental Claims

IL203171 was filed with the Israel Patent Office (ILIPO) and appears to focus on a specific drug formulation or therapeutic method. While the full patent document provides complex legal and technical language, the core scope revolves around:

  • A novel chemical compound or a pharmaceutically active formulation.
  • A method of treatment utilizing the compound.
  • Specific dosage forms, administration routes, or combination therapies.

Core Claims Breakdown

  1. Chemical Composition Claims:
    These typically define the compound’s structure, including key functional groups or stereochemistry, setting fundamental boundaries for what constitutes infringement.

  2. Method of Use Claims:
    These describe therapeutic methods, such as administering the compound to promote a specific pharmacological effect, often with particular dosage regimes or patient populations.

  3. Formulation and Delivery Claims:
    Such claims involve specific excipients, formulations, or delivery mechanisms (e.g., controlled-release, topical application), which can extend patent protection to practical drug products.

  4. Intermediate or Production Method Claims:
    These detail manufacturing processes or intermediates that lead to the claimed active compound, offering additional layers of protection.

Legal and Technical Evaluation:
The breadth of the claims depends on how narrowly or broadly they are drafted. Broad claims covering generic classes or mechanisms may face challenges based on prior art, whereas narrow claims about specific compounds or methods are easier to defend but limit the scope.

Patent Landscape in Israel and International Context

Israel’s Pharmaceutical Patent Environment

Israel maintains a robust patent system aligned with international standards, and its pharmaceutical patent landscape is characterized by several strategic features:

  • Strong Patent Enforcement:
    Enhanced by effective judicial mechanisms and specialized patent courts.

  • Innovation Hub:
    Israel’s biotech sector fosters continuous innovation, with patents often focusing on novel small molecules, biologics, or formulations.

  • Patent Term & Data Exclusivity:
    The patent term is typically 20 years from the filing date, with data exclusivity provisions further protecting innovative pharmaceutical data.

Competitive Patent Landscape

In relation to IL203171, relevant prior art includes:

  • Existing patents or patent applications for similar chemical classes and therapeutic methods.
  • Patent families from leading pharmaceutical innovators (e.g., Pfizer, Novartis, or local Israeli biotech firms).
  • International patents filed under the Patent Cooperation Treaty (PCT) concerning similar compounds or methods.

Patent Landscape Analysis

  • Overlap and Freedom-to-Operate:
    The patent’s claims must be distinguished from prior art. Narrower claims focusing on unique structural features or specific therapeutic methods are less vulnerable to invalidation.

  • Potential for Patent Thickets:
    Multiple overlapping patents around similar compounds or methods could complicate commercialization, necessitating careful freedom-to-operate analyses.

  • Patent Validity Concerns:
    Challenges relating to novelty, inventive step, or sufficient disclosure may emerge, particularly if similar compounds are disclosed in the literature.

International Patent Strategy

Given Israel’s small market size but strategic research presence, patent owners often file corresponding patents in major jurisdictions—such as the US, EU, China, and Japan—to secure global exclusivity. The scope of IL203171 guides such international filings by defining key inventive features that inform claims drafting and priority claims.

Implications for Stakeholders

  • Pharmaceutical Developers:
    Need to analyze IL203171’s claims to assess infringement risks when developing similar treatments.

  • Patent Attorneys:
    Should evaluate claim scope for validity and potential challenges, advising on patent filing strategies.

  • Investors and Licensors:
    Must monitor patent landscape evolution to inform licensing, partnership negotiations, or fallback strategies.

  • Generics and Competitors:
    Will scrutinize the claims to identify workarounds, designing around strategies or challenging patent validity.

Conclusion

Israel Patent IL203171 encompasses a strategically significant scope, centered on specific chemical or therapeutic innovations. Its claims define a protected niche within the pharmaceutical patent landscape, emphasizing a careful balance between broad protection and defensibility against prior art. Given Israel’s active biotech environment and international patent practices, IL203171’s value hinges on precise claim drafting, comprehensive landscape analysis, and proactive patent strategies.


Key Takeaways

  • The patent’s scope depends heavily on the drafting of claims concerning chemical structure, therapeutic use, and formulation.
  • Israel’s patent environment offers robust protection but demands clear novelty and inventive step, especially amid overlapping prior art.
  • Strategic international filings are essential to maximize protection and market exclusivity for the innovation.
  • Careful analysis of the patent landscape can prevent infringement risks and identify avenues for licensing or patent challenges.
  • Vigilance in monitoring competing patents can facilitate adaptive strategies in R&D and commercialization.

Frequently Asked Questions (FAQs)

1. What distinguishes IL203171 from prior art?
IL203171 claims a novel compound or therapeutic method with unique structural or functional features that were not previously disclosed, establishing its novelty.

2. How broad are the claims typically in such patents?
Without the full document, the scope can range from narrowly defined specific compounds to broader classes of structurally related molecules, depending on claim drafting.

3. Can IL203171 be challenged for patent validity?
Yes. Challenges can be based on prior art disclosures, lack of inventive step, or insufficient disclosure, especially if similar compounds exist in scientific literature.

4. What is the importance of filing international applications?
International filings extend patent protection beyond Israel, capturing markets like the US, EU, China, and Japan, crucial for commercial success.

5. How does IL203171 impact generic drug development?
If maintained, the patent can delay generic entry for the protected formulation or method, incentivizing investment in innovative treatments.


Sources:

  1. Israel Patent Office Patent Database.
  2. World Intellectual Property Organization (WIPO) Patent Landscape Reports.
  3. Israeli Patent Law and Practice Reports.
  4. Pharmaceutical Patent Law and International Filing Strategies.
  5. Patent Examination Guidelines for Pharmaceutical Innovations.

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