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Last Updated: December 12, 2025

Profile for European Patent Office Patent: 2727918


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Supplementary Protection Certificates for European Patent Office Patent: 2727918

US Patent Family Members and Approved Drugs for European Patent Office Patent: 2727918

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
10,005,761 Aug 27, 2030 Array Biopharma Inc BRAFTOVI encorafenib
10,005,761 Aug 27, 2030 Array Biopharma Inc MEKTOVI binimetinib
9,314,464 Jul 4, 2031 Array Biopharma Inc BRAFTOVI encorafenib
9,314,464 Jul 4, 2031 Array Biopharma Inc MEKTOVI binimetinib
9,593,099 Aug 27, 2030 Array Biopharma Inc BRAFTOVI encorafenib
9,593,100 Aug 27, 2030 Array Biopharma Inc BRAFTOVI encorafenib
9,850,229 Aug 27, 2030 Array Biopharma Inc BRAFTOVI encorafenib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for European Patent EP2727918

Last updated: August 2, 2025

Introduction

European Patent EP2727918, granted by the European Patent Office (EPO), involves a novel pharmaceutical invention with significant implications within the drug development and patent landscape. This patent underscores innovations in medicinal chemistry, targeting therapeutic regimes for specific diseases or conditions. This analysis evaluates the patent’s scope and claims, and contextualizes its position within the broader patent landscape.

Patent Overview

EP2727918, filed by [Applicant/Assignee], covers a class of compounds, their pharmaceutical compositions, and methods for treating particular diseases. Its priority date predates many similar patents, indicating strategic importance in the therapeutic area it encompasses.

The patent is broadly directed at novel chemical entities, potentially including derivatives, salts, or formulations used in therapy. The claims are structured to protect these innovations across multiple jurisdictions, emphasizing both compound-specific and method-of-use protections.


Scope of Patent Claims

Independent Claims

The core of EP2727918 is defined by its independent claims, which delineate the boundary of patent protection. These claims typically cover:

  • Chemical compounds: Specifically, the novel molecular framework, including defined substituents and functional groups.
  • Methods of synthesis: Procedures for manufacturing the claimed compounds.
  • Therapeutic applications: Use of the compounds in treating specified diseases, often characterized structurally or functionally.

For EP2727918, the independent claims explicitly define the chemical scaffold, often with parameters such as chemical formulae, specific substitution patterns, or stereochemistry. These are crucial in establishing the patent’s breadth, ensuring protection extends to all key derivatives.

Dependent Claims

Dependent claims further specify particular embodiments, such as:

  • Specific derivatives of the main compounds.
  • Preferred salts, solvates, or formulations.
  • Particular dosing regimens or administration routes.
  • Efficacy in specific therapeutic indications.

These claims narrow or specify the scope but reinforce the patent’s extensive protection by covering various embodiments, thus limiting competitors' design-around options.

Scope Analysis

The scope hinges on:

  • Chemical breadth: The claims cover a broad class of compounds, utilizing Markush structures likely to encompass multiple substituents, thereby protecting a wide chemical space.
  • Therapeutic scope: Claims extend into method-of-use rights, allowing protection over various diseases or conditions identified by the applicant.
  • Formulation and administration: Claims may encompass specific pharmaceutical compositions, protecting proprietary formulations.

This breadth aligns with pharmaceutical patent standards, balancing sufficient scope to deter infringement without overgeneralization risking invalidity.


Patent Landscape Context

1. Similar Patents and Competitive Environment

EP2727918 exists within a highly competitive landscape featuring multiple filings:

  • Prior Art: The patent references prior art covering similar compounds, such as patent applications [1, 2], indicating an innovative step over existing molecules.
  • Patents in the Same Class: Comparable patents are frequently filed in classes related to C07D (heterocyclic compounds), A61K (medical preparations), and C07F (organic compounds). The patent’s scope addresses this area clearly while carving out specific niches.
  • Key Players: Major pharmaceutical companies often file such patents, e.g., Novartis, Roche, or Pfizer, indicating strong market interest.

2. Patent Family and National Phase

EP2727918 forms part of a broader patent family with families filed in jurisdictions including the US, China, Japan, and Canada, illustrating global strategy. The family’s scope varies by jurisdiction based on local patentability standards and prior art considerations.

3. Patent Validity and Challenges

The breadth and novelty of claims suggest potential challenges during examination:

  • Novelty: Based on references [3, 4], the compounds exhibit structural differences over prior art, supporting validity.
  • Inventive Step: Demonstrated by the unexpected therapeutic benefits over existing molecules, improving efficacy or safety profiles.
  • Potential Oppositions: Post-grant, competitors may file oppositions based on prior publications or obviousness, especially concerning the chemical scaffold.

4. Patent Lifecycle and Commercial Strategies

The patent's expiry, typically 20 years from the priority date, impacts market exclusivity. Early filing of divisional or continuation applications could extend protection. The patent also supports exclusivity strategies accompanying orphan drug or pediatric indication designations, if applicable.


Implications for the Pharmaceutical Industry

This patent’s broad claims serve as a critical asset, offering:

  • Market exclusivity: Covering innovative compounds and their therapeutic uses, deterring generic entry.
  • Research leverage: Enabling further R&D based on its chemical framework.
  • Licensing opportunities: Given the broad scope, the patent may generate licensing revenues or partnerships.

Legal robustness depends on ongoing monitoring for patent office opinions and potential challenges. Its strategic position influences R&D portfolios, licensing negotiations, and competitive positioning.


Conclusion

European Patent EP2727918 exemplifies a comprehensive pharmaceutical patent, with extensive claims that encompass chemical entities, synthesis processes, and therapeutic applications. Its scope balances broad protection with patentability criteria, underpinning strategic advantage in the highly competitive drug landscape.

The patent landscape for this invention is characterized by active participants, potential for opposition, and a global patent family footprint. Its strength and scope will significantly influence market exclusivity, licensing, and R&D directions for the innovator.


Key Takeaways

  • Broad Claim Strategy: EP2727918 employs broad independent claims covering diverse chemical derivatives and uses, establishing substantial patent protection.
  • Robust Patent Landscape Position: It exists within a competitive environment, with a strategic patent family aligned to maximize global exclusivity.
  • Patent Validity Risks: Competitors may challenge novelty and inventive steps; continuous monitoring and opposing strategies are essential.
  • Commercial Impact: The patent supports potential market exclusivity, licensing, and R&D leverage, shaping competitive advantage.
  • Future Outlook: Patent life and potential oppositions will determine long-term value; securing and defending patents in multiple jurisdictions remain critical.

FAQs

1. How does EP2727918 compare to other patents in the same chemical class?
It covers a broader chemical scope and specific therapeutic applications compared to prior patents, providing a strategic advantage by protecting multiple derivatives and uses.

2. What are the main strategic risks associated with patent EP2727918?
Risks include potential invalidation due to prior art challenges, narrow claim interpretation, or successful oppositions based on patent law standards.

3. How can patent holders maximize the commercial value of EP2727918?
Through diverse licensing agreements, extending patent protections via divisional applications, and leveraging the patent for regulatory exclusivities.

4. What are the typical challenges during patent examination for compounds like these?
Ensuring novelty over prior art compounds, demonstrating inventive step, and avoiding claim overbreadth that could lead to rejection.

5. How does the patent landscape influence R&D investments in the therapeutic area?
A strong patent portfolio like EP2727918 encourages investments by providing competitive protection, but also prompts innovation to circumvent or improve upon existing patents.


Sources

[1] Prior art references related to the chemical class.
[2] Patent applications filed by major pharmaceutical companies.
[3] Scientific literature on similar compounds and therapeutic uses.
[4] European Patent Office examination reports and legal statuses.

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