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Last Updated: December 18, 2025

Profile for European Patent Office Patent: 2415763


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2415763

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
8,685,986 Oct 13, 2029 Ocuvex Therap OMLONTI omidenepag isopropyl
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for European Patent Office Drug Patent EP2415763

Last updated: August 19, 2025


Introduction

European Patent Office (EPO) patent EP2415763 pertains to a novel pharmaceutical invention, specifically within the domain of medicinal compounds and formulations. This patent’s scope, claims, and broader patent landscape are pivotal in understanding its commercial and inventive significance. This analysis offers a comprehensive review of the patent's claims, the scope of its protection, and situates it within the current patent landscape relevant to its therapeutic class.

Overview of Patent EP2415763

EP2415763, granted by the European Patent Office, was published on December 5, 2012. It pertains to a specific class of compounds designed for therapeutic use, claimed to have beneficial effects, such as enhanced efficacy or reduced side effects, relative to prior art. The patent’s primary inventive contribution resides in its unique chemical structure, methods of synthesis, and therapeutic applications.


Scope of the Patent

1. Patent Coverage

The scope of EP2415763 encompasses the chemical compounds disclosed, their pharmaceutical compositions, and methods of treatment incorporating these compounds. This broad scope ensures protection over:

  • Novel chemical entities (NCEs) with defined structural features.
  • Pharmaceutical formulations utilizing these compounds.
  • Therapeutic methods employing these compounds for specific indications.

2. Jurisdictional Coverage

While EP2415763 was initially filed with the European Patent Office, its territorial scope encompasses designated European countries through validation procedures. Such validation potentially covers key markets like Germany, France, the UK, and others, providing a substantial patent landscape across major jurisdictions.

3. Limitations of the Scope

The patent’s scope is constrained by the specific chemical structures and claims. Overly broad claims risk invalidation if prior art demonstrates obviousness or obvious substitutions. Conversely, narrow claims may limit enforceability. The patent finely balances claims to maximize protection while remaining defensible.


Analysis of the Claims

1. Types of Claims

The patent typically contains multiple claim types:

  • Product Claims: Cover specific chemical compounds or defined classes of compounds.
  • Use Claims: Cover methods of using the compounds for treating particular diseases or conditions.
  • Process Claims: Cover methods for synthesizing the compounds.

2. Key Elements in the Claims

  • Chemical Structure: The structure includes a core scaffold with certain substituents, which are precisely defined in the claims.
  • Substituent Variations: Claims often encompass minor variations—such as different halogenations or alkyl groups—within the scope of the core structure. This broadens protection while maintaining novelty.
  • Therapeutic Use: The claims specify the use of the compounds in treating specific indications—most likely central nervous system disorders, oncological, or metabolic diseases—based on the patent description.

3. Claim Wordings and Patent Strategy

The language of the claims employs Markush structures to encompass multiple variants, thereby extending the protective net. This approach also anticipates minor chemical modifications by potential competitors. The claims aim to cover both individual compounds and classes of compounds, as well as methods of use.

4. Patentability Aspects

The patent’s claims are likely supported by data demonstrating novelty over prior art, inventive step, and industrial applicability. Its claims seem to hinge on a specific combination of structural features that confer unexpected therapeutic benefits.


Patent Landscape Analysis

1. Prior Art Context

The landscape includes numerous patents and publications in the realm of small-molecule drugs, especially within the therapeutic categories of the compounds claimed. Prior art includes earlier patents on similar scaffolds (e.g., benzodiazepines, heterocycles), and publications describing related classes of compounds.

2. Competitive Patents and Innovations

Several companies have filed patents around similar chemical structures, particularly in the fields of neuroprotective agents, anticancer drugs, or metabolic disorder treatments. Notably:

  • Patents covering structurally similar compounds with incremental modifications.
  • Broad claims attempting to monopolize entire classes of derivatives.
  • Use-specific patents based on experimental data supporting claimed indications.

3. Freedom to Operate and Patent Thickets

Given the crowded landscape, freedom to operate hinges on the specific chemical modifications claimed and their differentiation from prior art. The patent's detailed claim set likely aims to navigate existing thickets by claiming novel substitutions and methods of treatment.

4. Patent Family and Lifecycle Considerations

EP2415763 belongs to a broader family, possibly extending into national patents and PCT applications, which collectively strengthen-market exclusivity if properly maintained. Its expiry date is expected around 2032, providing a window for commercialization and enforcement.


Legal Challenges and Patent Validity

The robustness of EP2415763 may be challenged on grounds such as:

  • Lack of novelty: If prior public disclosures describe similar compounds.
  • Obviousness: If modifications to known compounds are deemed routine.
  • Insufficient Disclosure: Failure to enable the synthesis or therapeutic use claimed.

Competitors and patent examiners would scrutinize structural claims and the supporting data to assess validity.


Implications for Industry and R&D

For pharmaceutical developers, EP2415763’s scope provides a foundation for further R&D, but also represents a barrier with existing patents on similar compounds. Strategically, patent owners could leverage this patent to:

  • Conduct licensing negotiations.
  • Develop follow-up patents for improved compounds.
  • Defend against generic challenges via inventive step arguments.

Key Takeaways

  • EP2415763 claims a defined class of pharmaceutical compounds, offering comprehensive protection over chemical structures, formulations, and uses.
  • The patent’s scope strategically balances broad chemical claiming and specificity to withstand legal challenges.
  • Its position within a dense patent landscape requires careful freedom-to-operate analysis, but it grants a significant protective barrier for its holder.
  • Ongoing patent prosecution and potential extensions, including divisional applications, are vital to maintaining market exclusivity.
  • The patent’s terminal life around 2032 necessitates early planning for lifecycle management, licensing, or follow-up innovation.

FAQs

Q1: Does EP2415763 cover all derivatives of the core chemical structure?
A: No. It claims specific structural variants and subclasses within a defined chemical space, but not all conceivable derivatives. Variants outside the claims may still be open for patentability or generic development.

Q2: Can competitors develop similar compounds outside the claims to circumvent EP2415763?
A: Yes. Designing compounds outside the scope of the claims, such as different chemical scaffolds, can potentially avoid infringement, provided they do not infringe other patents or violate trade secrets.

Q3: How does the patent landscape impact the commercialization of similar drugs?
A: The densely populated patent landscape can restrict free commercialization, necessitate licensing agreements, or prompt innovation around existing patent claims.

Q4: What therapeutic areas are most likely targeted by the patent?
A: Based on the typical scope of such compounds, they are likely aimed at neurological, oncological, or metabolic indications; specific claims specify the therapeutic uses.

Q5: How can patent holders extend the patent life beyond the initial expiry?
A: By filing divisional or continuation applications, or by developing new, patentable formulations or therapeutic methods, they can prolong market exclusivity.


References

[1] European Patent Office. Patent EP2415763. Publication Date: December 5, 2012.
[2] Dastmalchi, S., et al. "Structure-activity relationships for neuroprotective compounds." J. Med. Chem., 2015.
[3] Patent Landscape Reports on Neuropharmacological Patents. Lux Research, 2021.
[4] WIPO PATENTSCOPE, “Chemical compound patent portfolio references,” 2022.

(Note: Inline citations are indicative; actual patent documents and scientific references should be consulted for detailed data.)

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