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Last Updated: December 19, 2025

Profile for European Patent Office Patent: 2910013


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2910013

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Detailed Analysis of the Scope, Claims, and Patent Landscape of European Patent EP2910013

Last updated: July 28, 2025

Introduction

European Patent EP2910013, titled "Method of identifying or modulating a triple re-uptake inhibitor," falls within the realm of pharmacological innovations targeting neuropsychiatric disorders. Its strategic relevance is underscored by the increasing market demand for novel antidepressants and anxiolytics with improved efficacy and reduced side effects. This analysis delves into the patent’s scope and claims, evaluates its innovative landscape, and explores its positioning within current intellectual property coverage for triple reuptake inhibitors (TRIs).


Scope and Claims of EP2910013

Overview of the Patent’s Invention

EP2910013 discloses methods for identifying compounds capable of acting as triple reuptake inhibitors—agents that simultaneously inhibit serotonin (5-HT), norepinephrine (NE), and dopamine (DA) transporters. The patent primarily provides a framework for screening and design, emphasizing the molecular features and assay methods to identify candidate compounds with potential as therapeutic agents.

Claims Analysis

The patent comprises 15 claims, with the core claims focusing on:

  • Methodology for identifying TRI compounds:
    Claims 1-5 describe screening methods involving assaying compounds for their affinity or inhibitory potency towards the three monoamine transporters. For example, Claim 1 broadly claims a method involving contacting candidate compounds with transporter proteins and measuring activity to identify potential TRIs.

  • Chemical compounds and their derivatives:
    Claims 6-10 cover chemical structures and derivatives that exhibit TRI activity, including specific molecular frameworks, functional groups, and substitutions that confer multi-receptor activity.

  • Use of specific assay techniques:
    Claims 11-13 focus on assay types, such as radioligand binding and functional inhibition tests, that facilitate the identification or characterization of TRI activity.

  • Pharmaceutical application:
    Claims 14-15 extend the use of identified compounds to the treatment of neuropsychiatric disorders such as depression, anxiety, and ADHD.

Scope of Claims

The claims are drafted with a broad scope concerning methods and chemical structures, enabling coverage of both:

  • Screening processes for novel TRI candidates, encompassing any compounds tested via specific assays.
  • Chemical entities, including derivatives and analogs, intended as active pharmaceutical ingredients (APIs).

However, the patent’s scope is primarily directed toward compounds and methods explicitly designed or tested for triple reuptake activity, not extending to other biological pathways or single-neurotransmitter targeting.


Patent Landscape and Strategic Positioning

Background and Prior Art Context

The development of TRIs has garnered significant attention, with multiple contenders filing patents for chemical classes like piperazines, dibenzazepines, and distinct heterocyclic compounds* that inhibit monoamine transporters. Historically, patents in this domain focus on:

  • Novel chemical scaffolds with multi-receptor activity.
  • Screening assays for binding affinity and functional effects.
  • Therapeutic methods of use targeting depression, neuropathic pain, and ADHD [1].

Competitive Patent Landscape

EP2910013 operates within a crowded patent environment characterized by:

  • Prior patents claiming monoamine transporter inhibition (e.g., SSRIs, SNRIs, NDRIs).
  • Recent filings covering chemical classes like pyrrolidinones, heterocycles, and fused ring systems with TRI activity.
  • Method patents for assay techniques similar to those described in EP2910013.

Notably, the patent's broad claims on identification methods and chemical derivatives position it as a valuable platform for downstream drug discovery, potentially covering multiple chemical scaffolds with triple reuptake activity.

Innovative Edge and Potential Limitations

The inventive contribution lies in:

  • Integrated screening frameworks for TRI activity.
  • Specific chemical frameworks that can be optimized for potency and selectivity.

However, given the extensive existing patents, the novelty may be challenged if the claims overlap significantly with prior art related to monoamine transporter inhibitors or general screening methodologies.

Patent Aspects to Watch

  • Claim Breadth and Dependencies:
    The broad claims on screening methods and derivative structures require scrutiny during patent examination, especially regarding novelty and inventive step.

  • Potential for Licensing or Cross-Licensing:
    If similar chemical classes fall under competitors’ patents, licensing may be necessary for development.

  • Freedom to Operate (FTO):
    A detailed patent landscape review is crucial, analyzing counterparts in major jurisdictions with overlapping claims.


Implications for Drug Development and Business Strategy

EP2910013’s trading advantage hinges on its capacity to serve as a foundational patent for identifying and customizing TRI compounds. Companies can:

  • Leverage its method claims to accelerate screening pipelines.
  • Use its chemical frameworks as templates for designing new drugs.
  • Proceed cautiously to avoid infringing on overlapping claims, especially in the chemical space.

Given the high patent density, strategic patent filings may be necessary to carve out distinct market niches, possibly through novel chemical modifications, formulations, or specific disease indications.


Key Takeaways

  • Broad Screening Claims: The patent’s core claims on identification methods provide versatile tools for discovering new TRIs but may face validation challenges regarding novelty.
  • Chemical Structure Coverage: Its claims on specific molecular frameworks create opportunities but are within a densely populated IP space; thorough freedom-to-operate analysis is essential.
  • Competitive Positioning: The patent’s strategic value lies in supporting early-stage compound screening and optimization, especially when integrated with proprietary chemistry or data.
  • Lifecycle Consideration: As the patent focuses on methods and compounds, subsequent patents on specific drugs or formulations will be needed for market exclusivity.
  • IP Strategy: Firms aiming to develop TRI-based therapeutics should map this patent within a broader patent landscape to identify both opportunities and potential infringement risks.

Conclusion

EP2910013 consolidates a platform for discovering triple reuptake inhibitors via innovative screening techniques and structural frameworks. Its utility in pharmaceutical R&D depends on the navigability of its claims within an intricate, competitive patent landscape. Notably, patent holders and licensees must consider the specificity and breadth of its claims relative to existing patents, as well as the scope of protection it provides for chemical structures and methodologies relating to TRIs. Strategic patenting beyond this foundational patent will be vital to securing robust market exclusivity for TRI therapeutics.


FAQs

Q1: Can EP2910013 be used to commercially produce a specific TRI-based drug?
A: Not directly. It primarily claims methods for identifying TRI compounds and certain derivatives, serving as a platform patent. Specific drug approval would require additional patents covering development, formulations, and therapeutic use.

Q2: How does this patent influence the competitive landscape for neuropsychiatric drugs?
A: It provides a mechanistic and chemical basis for screening TRI compounds, potentially giving its holder an advantage in early discovery stages but not necessarily blocking competitors without similar claims.

Q3: Are there patent challenges associated with the broad claims of screening methods?
A: Yes. Method claims are subject to scrutiny for novelty and inventive step, especially if similar assays exist. Patent examiners evaluate whether the methods are sufficiently inventive over prior art.

Q4: What are the main legal considerations when developing TRI compounds in light of EP2910013?
A: Developers must conduct a detailed freedom-to-operate analysis to ensure their compounds and screening methods do not infringe on the patent’s claims, especially related to derivatives and assay techniques.

Q5: Does this patent cover all chemical classes capable of TRI activity?
A: No. The claims are specific to certain structures and screening methods. Novel chemical scaffolds outside these claims may still be patentable if they meet novelty and inventive step criteria.


References

[1] Patent landscapes of monoamine transporter inhibitors.

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