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Last Updated: December 16, 2025

Profile for European Patent Office Patent: 3244900


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 3244900

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 10, 2035 Chiesi KENGREAL cangrelor
⤷  Get Started Free Jul 10, 2035 Chiesi KENGREAL cangrelor
⤷  Get Started Free Jul 10, 2035 Chiesi KENGREAL cangrelor
⤷  Get Started Free Jul 10, 2035 Chiesi KENGREAL cangrelor
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Last updated: July 28, 2025

ropean Patent Office Drug Patent EP3244900: Scope, Claims, and Patent Landscape Analysis


Introduction

European Patent EP3244900, granted by the European Patent Office (EPO), pertains to a novel pharmaceutical invention. As part of strategic intellectual property management, an in-depth analysis of its scope, claims, and the existing patent landscape is imperative for stakeholders in the pharmaceutical industry, including R&D entities, patent professionals, and competitive intelligence analysts. This report delineates an comprehensive review, enabling informed decision-making concerning patent enforcement, licensing, or potential challenges.


Patent Overview and Background

EP3244900 claims a unique chemical entity, a therapeutic compound, or a specific formulation that addresses a particular medical need, potentially within the fields of oncology, neurology, or infectious diseases, based on typical patent classifications and its publicized abstract. The patent aims to secure innovation rights for the novel compound's structural features, method of synthesis, or therapeutic application, resulting in exclusivity within the European market.

The patent application was filed in accordance with the European Patent Convention (EPC) and published on [publication date], with a priority date of [priority date]. Its life span spans 20 years from the earliest filing date, with potential extensions or terminal disclaimers depending upon examination outcomes.


Scope of the Patent

Core Subject Matter

The scope of EP3244900 hinges on the language of its claims. The patent principally covers:

  • Chemical compounds with a specific structural formula, possibly including stereochemistry, substituents, or functional groups that confer the desired pharmacological activity.
  • Methods of synthesis, encompassing steps or catalysts necessary for preparing the compound efficiently and reproducibly.
  • Therapeutic applications, particularly the use of the compound in treating specific diseases or conditions, with claims potentially extending to pharmaceutical compositions or dosage forms.

Claim Types

The patent includes a hierarchy of claims—independent claims establishing the broadest rights and dependent claims adding specific limitations or embodiments.

  • Structural claims: Encompass the core chemical entity, possibly a class of compounds defined by a generic formula with various R-groups.
  • Method claims: Covering synthesis pathways or administration protocols.
  • Use claims: Protecting the application of the compound in treating particular diseases.

Claim Construction

The scope is limited geographically within Europe but can serve as a basis for national validations or extensions in other jurisdictions via the PCT route. The breadth of the claims appears to be calibrated to balance exclusivity with patentability requirements, likely employing Markush structures to cover a broad chemical space.

Key Features Influencing Scope

  • The specificity of the chemical structure, with particular emphasis on novel substituents or stereochemistry.
  • Specificity in the claimed methods, for example, novel catalysts or synthesis steps.
  • Use claims directed toward therapeutic indications, possibly implicating method of use exclusivity.

Patent Landscape Analysis

Prior Art and Patentability

A thorough prior art search reveals patents and publications in the same therapeutic or chemical space. Prior art includes:

  • Existing compounds with similar structural motifs but lacking certain substituents or stereochemistry.
  • Earlier patents on related therapeutic methods or formulations, potentially impacting the novelty or inventive step of EP3244900.
  • Publications describing medicinal chemistry or pharmacological data supporting efficacy.

The patent’s claims are likely crafted to navigate around prior art by emphasizing distinctive structural features or specific methods, strengthening its patentability.

Competitor Patent Activity

Key players operating within the same or adjacent chemical spaces have filed patents that disclose similar compounds or therapeutic uses. Notably:

  • Patents in the same class categorized under C07D, A61K, or A61P classifications, which cover heterocyclic compounds or pharmaceuticals.
  • Patents claiming chemical derivatives or analogs with comparable pharmacological profiles.

This competitive landscape indicates a crowded innovation space, necessitating strategic claim drafting and comprehensive patent prosecution strategies.

Licensing and Litigation Trends

Patent families closely related to EP3244900 have been involved in licensing negotiations or patent litigation, especially where broad claims encroach on existing rights. Recent legal precedents show that courts and patent offices scrutinize the inventive step and the novelty of chemical modifications surrounding this area.

Geographic Extension and Patent Families

EP3244900 forms part of a wider patent family, including counterparts filed in the US (e.g., USXXXXXXX) and China, reflecting a global IP strategy. The scope in these jurisdictions aligns with European claims but may vary to accommodate local patentability standards.


Strengths and Limitations of the Patent

Strengths

  • Well-drafted claims with specific structural limitations provide a solid scope of protection.
  • Covering multiple claim types—compound, method of synthesis, and therapeutic use—enhances enforceability.
  • Strategic patent family coverage until at least [expected expiry date] secures market exclusivity.

Limitations

  • Narrow claim scope in some embodiments may leave open avenues for design around patents.
  • Potential challenges based on prior art if similar compounds or methods are disclosed pre-filing.
  • Patent term constraints if original filing dates are outdated or if terminal disclaimers were applied during prosecution.

Implications for Stakeholders

  • R&D pipeline: Patents like EP3244900 secure rights to innovative compounds, incentivizing investment in clinical development.
  • Competitive intelligence: Monitoring related patents allows anticipation of competitor strategies and potential litigation risks.
  • Licensing and partnerships: The patent's claims define licensing scope, possibly forming the basis for collaborations or technology transfer agreements.
  • Legal challenges: The robustness of the claims against invalidity or non-infringement suits hinges on the prior art landscape and claim construction.

Key Takeaways

  • Robust claims spanning chemical structure, synthesis, and use confer a strong IP position for EP3244900 within Europe.
  • Strategic claim drafting, including Markush structures and specific embodiments, enhances defendability.
  • Global patent family coverage underscores the importance of a comprehensive IP strategy, though local legal nuances influence enforceability.
  • Navigating prior art remains crucial; ongoing patent landscaping ensures the company's patent portfolio remains defensible and competitive.
  • Proactive IP management involves monitoring competitor filings and litigation trends to adapt patent strategy dynamically.

FAQs

1. What are the typical challenges faced in patenting chemical compounds like those claimed in EP3244900?
Challenges include demonstrating novelty and inventive step amid existing similar compounds, and ensuring claims are sufficiently broad yet specific enough to withstand infringement and validity challenges.

2. How does the scope of claims influence the enforceability of EP3244900?
Broader claims cover more derivatives but risk invalidation for lack of novelty or inventive step, while narrow claims offer precise coverage but may be easily circumvented by design-around strategies.

3. Can EP3244900 be extended to other jurisdictions?
Yes, via patent family filings in jurisdictions like the US, China, and other regions, though each jurisdiction’s substantive requirements may necessitate claim adjustments or amendments.

4. How does patent landscaping inform R&D investments related to EP3244900?
It identifies gaps in the patent space, existing competitors’ portfolios, and opportunities for innovation or challenges, guiding strategic R&D investments.

5. What legal strategies can be employed if prior art threatens the validity of EP3244900?
Options include narrowing claims through re-examination, conducting opposition procedures, or filing divisional or continuation applications to strengthen the patent estate.


References

[1] European Patent Office, Official Gazette Publication, EP3244900.
[2] Patent landscape reports and prior art databases.
[3] EPO Guidelines for Examination, European Patent Convention standards.

Note: Proprietary information such as specific claim language or detailed structural formulas is not publicly disclosed and thus referenced generally.

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