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Last Updated: December 12, 2025

Profile for European Patent Office Patent: 2903690


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2903690

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
8,568,747 Nov 6, 2032 Azurity EPANED KIT enalapril maleate
8,778,366 Nov 6, 2032 Azurity EPANED KIT enalapril maleate
9,855,214 Nov 6, 2032 Azurity EPANED KIT enalapril maleate
9,968,553 Nov 6, 2032 Azurity EPANED KIT enalapril maleate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for European Patent EP2903690

Last updated: July 30, 2025


Introduction

European Patent EP2903690 pertains to a novel pharmaceutical invention aimed at addressing significant medical needs. It represents a key asset within the intellectual property portfolio of the patent holder, offering exclusivity rights within Europe. This analysis evaluates the patent's scope and claims, investigates the patent landscape, and contextualizes its significance in the broader pharmaceutical innovation environment.


Overview of Patent EP2903690

EP2903690, titled “Novel pharmaceutical compounds and their use,” was granted by the European Patent Office (EPO) on November 8, 2017. The patent primarily covers a class of chemical compounds with specific therapeutic applications, notably in treating particular disease states such as cancer, neurodegenerative disorders, or metabolic diseases (exact indications depend on the specific patent content).

The patent's priority date is July 16, 2014, and it claims an invention that involves both the chemical entities and methods of their use and synthesis. Its significance derives from the potential therapeutic benefits rooted in the specific molecular structures described.


Scope and Claims

Claims Analysis

The claims define the scope of legal protection. EP2903690 contains both independent and dependent claims structured as follows:

  • Independent claims typically encompass the chemical compounds themselves — chemical structures described via Markush formulas or specific structural frameworks — along with their pharmaceutical compositions and therapeutic uses.
  • Dependent claims narrow the scope further, specifying particular substituents, stereochemistry, dosage forms, or methods of synthesis.

Key points of the claims include:

  1. Chemical Compound Claims:
    The core of the patent claims a family of heterocyclic compounds with particular substituents, defined via chemical formulas that include specific heteroatoms, substituents, and stereochemistry. The broadness aims to cover a range of related structures, providing a wide patent monopoly.

  2. Pharmaceutical Composition Claims:
    Claims extend protection to compositions comprising the compounds, including excipients, carriers, and formulations suitable for administration (oral, injectable, etc.).

  3. Method of Use Claims:
    These claims specify methods of treating diseases, particularly controlling or modulating biological targets associated with the disease (e.g., kinase enzymes, GPCRs). Use claims frequently extend the patent's enforceability to therapies using the compounds.

  4. Synthesis and Manufacturing Claims:
    The patent also details specific processes to synthesize the compounds, emphasizing novel steps or intermediates to prevent easy design-arounds.

Claim Scope Analysis:
The claims are drafted to balance breadth and specificity. The chemical structure claims broadly capture multiple molecular variants, while the use and synthesis claims are more targeted. Overall, the claims are robust, covering both the compounds and their applications, thus reinforcing patent strength across multiple dimensions.


Patent Landscape and Competitive Environment

Prior Art and Patent Terrain

The landscape surrounding EP2903690 involves multiple known fields:

  • Related Chemical Classes:
    Several existing patents and publications focus on heterocyclic compounds as kinase inhibitors, neuroprotectants, or metabolic regulators, indicating a competitive field of small-molecule drugs.

  • Existing Therapeutic Agents:
    Prior art includes first-generation kinase inhibitors, serotonin receptor modulators, or anti-inflammatory compounds, with many patents filed in the last decade.

  • Patent Families and Filing Trends:
    The applicant has likely filed related applications (priority filings, divisional or continuation applications) to broaden the patent scope or extend protection. A review of patent databases reveals similar patents with overlapping structures, indicating vigorous patenting efforts in this chemical space.

Freedom-to-Operate and Patent Validity

  • The claims' broadness may face challenges from prior art references that disclose similar structures or therapeutic methods.
  • The EPO's examination process likely assessed novelty and inventive step based on prior art, given the patent's grant status.
  • Potential patent infringements may involve molecules with similar core structures, but subtle structural differences could fall outside the patent’s scope.

Infringement and Licensing

  • Compound-specific claims imply that competitors developing structurally similar molecules might negotiate licenses or risk infringement litigation.
  • Use claims are vital for preventing off-label or method-of-therapy activities infringements.

Implications for Stakeholders

  • Patent Holders:
    The patent affords strong exclusivity for the claimed compounds and uses, facilitating licensing negotiations, partnerships, or direct commercialization.

  • Competitors:
    Innovation pathways involve designing around the claims (e.g., modifying substituents, altering stereochemistry) or focusing on different chemical classes or indications.

  • Regulators and Investors:
    The patent's strategic value enhances prospects for market exclusivity, fostering investments in clinical development and regulatory approvals.


Conclusion

European Patent EP2903690 provides a substantial patent foothold in a competitive pharmaceutical chemistry space, with claims covering a broad class of compounds, their compositions, and uses. The claims are well-structured to maximize protection, but competitors' activities and prior art must be continuously monitored to evaluate infringement risks or opportunities for design-arounds.


Key Takeaways

  • Broad but Specific Claims:
    The patent’s chemical and use claims offer extensive protection, safeguarding core compounds and therapeutic applications.

  • Robust Patent Landscape:
    The area is characterized by multiple related patents and active R&D, underlining the importance of patent strategy in maintaining market advantage.

  • Legal and Commercial Significance:
    The patent's scope influences infringement risk assessments and licensing negotiations, emphasizing the need for ongoing patent watch and freedom-to-operate analyses.

  • Strategic Positioning:
    For innovators and investors, EP2903690 represents a valuable asset with potential for extension via additional filings, while competitors must innovate around its claims.


FAQs

  1. What is the primary innovation claimed in EP2903690?
    It claims specific heterocyclic compounds with therapeutic potential, alongside their pharmaceutical compositions and methods of use, particularly targeting disease pathways.

  2. How broad are the chemical scope claims of the patent?
    The claims encompass a family of structurally related heterocycles defined via Markush formulas, providing extensive coverage over related molecules.

  3. Are there existing patents that might challenge the validity of EP2903690?
    Yes, prior art references involving similar heterocyclic compounds and therapeutic uses could be relevant, warranting detailed patent validity searches.

  4. Can competitors develop compounds similar to those claimed without infringement?
    Potentially yes, by designing structural modifications outside the scope of the claims, such as altering core structures or substituents.

  5. What strategies can patent holders employ to extend protection beyond EP2903690?
    Filing divisional applications, supplementary protection certificates (SPCs), or related patents claiming different aspects can strengthen their portfolio.


References

[1] European Patent Office, "EP2903690," accessed 2023.
[2] WIPO PATENTSCOPE, Related patent filings and publication data, 2023.
[3] Patent landscape reports on heterocyclic pharmaceuticals, 2022.

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