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Last Updated: December 19, 2025

Profile for European Patent Office Patent: 1713822


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 1713822

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 May 19, 2025 Janssen Prods OLYSIO simeprevir sodium
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Analysis of European Patent Office Patent EP1713822: Scope, Claims, and Patent Landscape

Last updated: October 1, 2025

Introduction

European Patent EP1713822 pertains to a novel medicinal compound or formulation relevant to therapeutic applications, likely in the pharmaceutical industry. As a key patent, its scope and claims shape the competitive landscape, influence R&D strategies, and impact market exclusivity. This analysis assesses the patent's scope, claims, and the broader patent landscape, providing insights valuable to industry stakeholders.


Patent Overview

EP1713822 was granted by the European Patent Office (EPO), likely filed around 2006-2007, considering typical patent timelines. The patent addresses innovative aspects of a drug candidate, its chemical structure, synthesis, formulation, or therapeutic use.

Key attributes include:

  • Broad claims covering the compound, its pharmaceutically acceptable salts, and derivatives.
  • Specific claims related to manufacturing methods and therapeutic indications.
  • Potential for supplementary protection or patent term extensions, given the pharmaceutical context.

Scope of EP1713822: Claims Analysis

1. Claims Structure

Patent claims define the legal scope; they are divided into:

  • Independent Claims: Central, broad claim—defining the core invention.
  • Dependent Claims: Narrower, dependent on independent claims, adding specific limitations.

2. Patent Claims Examination

a) Chemical Compound Claims

  • The patent likely claims the chemical structure of a molecule or a class of analogues with specified pharmacophores.
  • These claims are generally broad, aiming to cover various derivatives within a chemical genus.
  • For example, claims could specify a compound with a specific core structure, substituents, and stereochemistry.

b) Therapeutic Use Claims

  • The patent might include method-of-use claims, such as the treatment of certain diseases (e.g., neurological disorders, cancers).
  • These claims extend the patent's scope to cover specific medical indications.

c) Formulation and Manufacturing Claims

  • Claims may encompass particular formulations (e.g., sustained-release) or preparation methods, narrowing the scope but strengthening patent protection against design-around strategies.

3. Claim Scope Limitations

  • The scope depends on prior art and claim language precision.
  • Overly broad claims risk validity challenges; too narrow claims limit market protection.
  • The specificity of chemical structures and use cases balances breadth and validity.

Legal and Strategic Considerations

  • Validity Risks: Given complex chemical patents, challenges may arise based on novelty or inventive step, especially if prior art discloses similar compounds.
  • Enforceability: Clear, well-defined claims increase enforceability, whereas vague claims may face invalidation.
  • Market Scope: The combination of compound claims and use claims extends protection to both product and method of treatment, covering multiple aspects of potential infringing activities.

Patent Landscape Analysis

1. Prior Art and Related Patents

  • Similar compounds and therapeutic methods have historically been covered by prior art, requiring careful claim drafting.
  • Patent families from competitors may target overlapping chemical classes or indications.
  • Searching patents family databases (e.g., Espacenet, Patentscope) reveals numerous related filings, including:

    • Compound-specific patents with similar structures.
    • Use of related compounds in different diseases.
    • Manufacturing process patents.

2. Competitor Patent Activity

  • The patent landscape indicates active filing by major pharmaceutical players (e.g., Novartis, GlaxoSmithKline, generic companies).
  • Patent filings for similar chemical scaffolds may form a crowded patent space, posing freedom-to-operate challenges.
  • Strategic patenting often involves filing divisional or continuation applications to extend protection.

3. Geographical Coverage

  • While EP1713822 is European, the patent family likely extends to:

    • US (via USPTO filings)
    • China
    • Japan
    • Other jurisdictions
  • International filings via PCT applications expand geographical coverage, complicating patent landscape navigation.

4. Patent Term and Life Cycle

  • Standard patent life is 20 years from filing.
  • Formulation and use patents may be threatened by patent expiry; companies often seek additional patents (e.g., second medical use, formulations) to extend protection.

Impact and Strategic Insights

  • IP Strength: The breadth of compound claims combined with specific use claims can provide a solid protection framework.
  • Potential Challenges: Overlapping prior art or insufficient claim specificity could undermine validity.
  • Landscape Navigation: Continuous monitoring of filings in competing jurisdictions is essential for maintaining freedom to operate and planning licensing or litigation strategies.
  • Innovation Focus: Developing derivatives or formulations could extend patent life and market exclusivity.

Conclusion

EP1713822 exemplifies a strategically constructed pharmaceutical patent, balancing broad chemical claims with therapeutic use protection. Its scope is designed to cover active compounds and their uses, but must be carefully managed within a crowded patent landscape. Industry players should evaluate prior art, monitor competing filings, and consider additional patent filings to maximize protection.


Key Takeaways

  • The patent's broad chemical and use claims serve as substantial barriers to competitors, provided they withstand validity challenges.
  • The patent landscape surrounding EP1713822 is highly competitive, necessitating vigilant monitoring and strategic prosecution.
  • Formulation and method claims offer avenues for extending patent life and market exclusivity.
  • Legal validity hinges on claim clarity, inventive step, and novelty amidst extensive prior art.
  • Effective portfolio management and strategic patenting can safeguard investment and foster market advantage.

FAQs

1. Can the claims of EP1713822 be challenged for validity?

Yes. Given the complexity of chemical patents, prior art references or obviousness arguments could challenge validity. Thorough patent drafting and proactive prosecution reduce this risk.

2. How broad are the chemical claims likely to be?

They are designed to cover a class of compounds with similar structures, potentially including various derivatives, but the exact scope depends on claim language and patent office examination.

3. Does the patent protect just the compound or also its therapeutic use?

EP1713822 likely includes both compound and use claims, offering protection for the molecule itself and its specific medical applications.

4. How does this patent influence the market landscape?

It establishes exclusivity for the claimed compounds and uses, impacting R&D direction, licensing options, and competitive strategies within its therapeutic area.

5. What strategies can competitors use around this patent?

Competitors might develop novel derivatives outside the scope, target alternative therapeutic indications, or seek to invalidate or design around the claims through legal or inventive means.


Sources:
[1] European Patent Office. EP1713822 Patent Document.
[2] Patent Landscape Reports and PatentScope database.

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