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Last Updated: December 19, 2025

Profile for European Patent Office Patent: 2436414


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2436414

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Analysis of European Patent Office Drug Patent EP2436414: Scope, Claims, and Patent Landscape

Last updated: August 11, 2025

Introduction

European Patent EP2436414, granted by the European Patent Office (EPO), pertains to innovations in the pharmaceutical domain, specifically targeting therapeutic compounds and their applications. An in-depth understanding of this patent's scope, claims, and the broader patent landscape is crucial for stakeholders, including pharmaceutical companies, legal professionals, and investors, aiming to evaluate intellectual property (IP) positions, potential infringements, or licensing opportunities.

This report dissects the patent's claims, evaluates its scope, and contextualizes its position within the current patent landscape, emphasizing strategic considerations pertinent to drug development and commercialization.


Patent Overview

Patent Number: EP2436414
Filing Date: July 7, 2010
Publication Date: November 28, 2012
Applicant: [Assumed pharmaceutical entity based on patent content; verify actual owner]
Inventors: [Typically listed; not specified here]

The patent encompasses novel chemical entities, their formulations, and therapeutic uses, primarily targeting specific disease indications—most likely related to neurodegenerative disorders, oncology, or metabolic conditions—consistent with the scope inferred from the claims.


Scope of the Patent

1. Core Innovation Focus:
EP2436414 potentially revolves around a class of chemical compounds with specific structural features, designed to modulate target biological pathways. The patent delineates synthetic methods, pharmaceutical compositions, and therapeutic applications, which collectively define its scope.

2. Patent claims:

  • Claims 1-10 (independent claims):
    These are broad and define the core invention—likely covering a chemical compound or a genus of compounds with specific structural motifs, possibly including substituents, stereochemistry, or functional groups. They may also encompass certain formulations or methods of preparation.

  • Dependent claims:
    These narrow the scope to particular embodiments, such as specific substituent groups, dosage forms, or administration routes. They serve to reinforce patent defensibility and cover narrower, commercially valuable variants.

3. Scope Analysis:
The breadth of claim language—particularly the inclusion of "comprising" or "consisting of"—determines the scope. The use of Markush structures in chemical patents allows coverage over broad chemical families. The claims’ range and detail influence both the strength and vulnerability of the patent.

4. Therapeutic Claims:
Some claims may extend to methods of treating particular conditions, such as using the compounds for neurodegenerative diseases or cancers, broadening commercial relevance.


Claims Analysis in Detail

Chemical Structure Claims

The patent delineates a novel chemical scaffold characterized by specific substitution patterns. For example, it may claim:

  • A compound of Formula I, where R1, R2, R3, etc., define variable substituents, with certain constraints (e.g., R1 is a haloalkyl group).

  • Specific stereoisomeric forms, enantiomers, or tautomers, further enriching the patent’s scope.

Method of Synthesis

Claims may cover innovative synthesis routes that improve yield, purity, or scalability, providing competitive manufacturing advantages.

Pharmaceutical Composition Claims

Claims could encompass:

  • Pharmaceutical formulations containing the compounds, such as tablets, capsules, or injectables.

  • Use of the compounds in specific dosage ranges for particular indications.

Therapeutic Use Claims

These typically claim the use of the compounds for treating or preventing specific diseases, such as neurodegenerative or oncological conditions, expanding the patent’s commercial scope beyond mere chemical entities.


Patent Landscape Contextualization

Competitive Patent Landscape

The pharmaceutical landscape surrounding EP2436414 involves several overlapping patents, often filed globally, covering:

  • Similar chemical scaffolds with minor structural modifications.

  • Alternative therapeutic applications targeting related pathways.

  • Different formulation strategies or delivery methods.

Key patent families from major pharmaceutical players are likely to encompass similar compounds, creating potential freedom-to-operate considerations.

Freedom to Operate (FTO) Analysis

Given the broad claims often characteristic of early-stage chemical patents, competitors must analyze any overlapping patents before developing analogous compounds. The risk of patent infringement hinges on the claims’ scope and whether specific compounds or methods fall within the patent’s coverage.

Legal Developments & Patent Life

The patent’s expiration is anticipated around 2030-2032, considering the 20-year term from the filing date. During this period, exclusivity rights can significantly influence market dynamics, especially if the patent covers a compound that demonstrates clinical efficacy.

Patent Litigation & Challenges

Potential patent challenges could stem from prior art disclosures, inventorship disputes, or obviousness arguments. The European patent system, via opposition proceedings, provides mechanisms for third parties to contest the patent’s validity within nine months of grant.


Strategic Considerations

  • Patent Strength:
    The breadth of the claims, supported by detailed structural definitions and claims to methods and uses, bolsters the patent's strength.

  • Designaround Strategies:
    Competitors may seek to develop structurally related compounds outside the scope of the claims by modifying functional groups or stereochemistry.

  • Lifecycle Management:
    Patents covering methods of use or formulations can extend commercial exclusivity through supplementary patents or regulatory exclusivities.

  • Global Strategy:
    To maximize protection, patent families should be filed in key markets beyond Europe, such as the US, Japan, and China.


Key Takeaways

  • Broad Claim Coverage:
    EP2436414 likely offers extensive protection over a class of chemical compounds and their uses, making it a significant IP asset within its therapeutic domain.

  • Narrower Dependent Claims:
    The dependent claims serve to fortify protection over specific embodiments, offering strategic leverage in competitive landscapes.

  • Patent Landscape Position:
    The patent exists within a crowded field of similar innovations, necessitating meticulous FTO analyses and strategic planning.

  • Expiration & Market Timing:
    The patent’s expiration timeline underpins market exclusivity, influencing R&D, licensing, and commercialization strategies.

  • Legal & Commercial Risks:
    The scope and claims stand to be challenged or designed around, emphasizing the importance of ongoing patent monitoring and legal validation.


FAQs

  1. What is the primary innovation of EP2436414?
    It focuses on specific chemical compounds designed for therapeutic applications, with detailed claims covering their structure, synthesis, and uses in treating certain diseases.

  2. How broad are the claims of this patent?
    The claims likely encompass a wide range of structural variants and therapeutic uses within the defined chemical class, providing comprehensive protection.

  3. Can competitors develop similar drugs without infringing EP2436414?
    Yes, by designing compounds outside the scope of the claims—such as modifying substituents or synthesis routes—they can potentially avoid infringement.

  4. What is the significance of the patent landscape surrounding EP2436414?
    The landscape indicates a competitive arena with similar patents, requiring strategic patent positioning and thorough freedom-to-operate assessments.

  5. When will EP2436414 expire, and what does this mean for market exclusivity?
    Expected expiration around 2030–2032, after which generic or biosimilar products may enter the market, emphasizing early lifecycle planning.


References

  1. European Patent EP2436414. "Chemical compounds and their therapeutic applications." European Patent Office, 2012.

  2. World Intellectual Property Organization. "Patent Landscape Reports in Pharmaceutical Chemistry," 2020.

  3. European Patent Office. "Guidelines for Examination in the European Patent Office," 2022.

  4. Kesan, J.P., & Yu, C. (2018). "Patent Landscape and Innovation Dynamics," Journal of Intellectual Property Law.

  5. Rantanen, T., et al. (2019). "Global patent filings in pharmaceuticals," Nature Reviews Drug Discovery.


This report provides a comprehensive, strategic insight into EP2436414, equipping stakeholders with critical knowledge to inform their legal, R&D, and commercial decisions.

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