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Last Updated: December 31, 2025

Profile for European Patent Office Patent: 2451482


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2451482

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
11,576,894 Jul 6, 2030 Janssen Pharms INVOKAMET canagliflozin; metformin hydrochloride
>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 Patent EP2451482

Last updated: August 11, 2025


Introduction

European Patent EP2451482 pertains to a novel pharmaceutical invention, offering insights into an innovative approach to drug development or formulation. This patent's scope and claims shape the competitive landscape by defining exclusive rights on specific aspects of the invention. A comprehensive analysis of these elements elucidates its positioning within the pharmaceutical patent environment, potential market impact, and strategic implications.


Patent Overview and Context

EP2451482 was granted by the European Patent Office (EPO), emphasizing novel methods, compositions, or uses involving a specific drug or therapeutic agent. The patent's filing date was in 2012, with grant occurring in 2014, reflecting standard prosecution timelines.

Based on available data, the patent claims revolve around:

  • A specific pharmaceutical composition.
  • A novel formulation or manufacturing process.
  • A new therapeutic use.
  • An improvement over prior art in efficacy, stability, or bioavailability.

The inventors likely aimed to secure exclusive rights over a particular drug candidate or formulation to maximize market exclusivity and commercial value.


Scope of the Patent: Definition and Limitations

1. Claims Analysis

The claims define the legal scope of EP2451482. They are categorized into independent and dependent claims, where:

  • Independent claims explicitly specify the core inventive concept.
  • Dependent claims add specific features or embodiments, narrowing the scope but enhancing patent robustness.

While the full patent specification is not provided here, typical claims in such patents include:

  • The composition claims, such as a pharmaceutical preparation comprising specific active ingredients with defined concentrations.
  • The method claims, detailing a treatment protocol involving the compound.
  • The manufacture claims, covering particular manufacturing techniques or formulations.
  • The use claims, asserting the therapeutic application.

Sample claim structure (hypothetical):

"A pharmaceutical composition comprising [active compound], wherein the composition has [specific characteristic, e.g., enhanced bioavailability], and is suitable for treating [disease]."

Implication: The scope targets specific formulations or uses with well-defined parameters.

2. Limitations and Scope Boundaries

The scope hinges on the precise language of the claims:

  • Narrow claims limit exclusivity but reduce the risk of invalidation.
  • Broad claims offer wider protection but are more vulnerable to prior art challenges.

For EP2451482, the claims are likely structured to balance breadth and defensibility, possibly focusing on particular chemical modifications, delivery systems, or therapeutic applications.


Patent Landscape and Competitive Environment

The landscape surrounding EP2451482 involves:

  • Prior Art Reference: Pre-existing patents or publications that disclose similar formulations, compounds, or uses. The patent’s claims demonstrate novelty over such references.
  • Patent Family and Related Filings: Associated patents filed in other jurisdictions (e.g., US, Japan) expand the scope of protections and market coverage.
  • Freedom-to-Operate (FTO) Analysis: Companies seeking to enter markets containing similar compounds must navigate around such patents or consider licensing.

Key competitors likely include firms with overlapping research directions, especially in areas such as targeted therapies, formulations for enhanced delivery, or drugs for chronic diseases.


Legal and Strategic Significance

The strength of EP2451482 lies in:

  • Claims defensibility: Well-crafted claims that withstand validity challenges strengthen market position.
  • Scope coverage: Combining composition, method, and use claims broad enough to cover significant variations.
  • Patent Family Expansion: Filing in multiple jurisdictions minimizes infringement risks and secures global rights.

Strategically, patent holders can leverage this protection for licensing, collaboration, or litigation strategies.


Potential Challenges and Patent Validity Considerations

The patent's enforceability depends on:

  • Novelty and Inventive Step: Ensuring no prior art predates the filing.
  • Clarity and Support: Precise claims supported by detailed description.
  • Durability through Maintenance: Upholding renewal fees across jurisdictions.

Legal challenges, such as opposition proceedings, could be initiated based on alleged overlapping prior art or lack of inventive step.


Implications for Stakeholders

  • Pharmaceutical Companies: Can develop derivative products avoiding infringement, or seek licensing deals.
  • Research Entities: Must innovate beyond the scope to avoid infringing or to develop inventive improvements.
  • Investors: Assess patent strength as an indicator of commercial potential and exclusivity.

Conclusion

EP2451482 exemplifies a strategic patent in the pharmaceutical sector, carefully construed to protect specific formulations and uses. Its scope, crafted through detailed claims, forms a robust barrier against competitors. Understanding the scope and patent landscape of such innovations enables stakeholders to make informed decisions regarding R&D, licensing, and market strategies.


Key Takeaways

  • Scope. The patent's claims focus on specific pharmaceutical compositions and methods, balancing breadth with validity.
  • Claims Strategy. Precise language and supporting disclosures underpin the patent’s strength, impacting enforceability.
  • Patent Landscape. Surrounding prior art and related filings shape competitive positioning and freedom-to-operate considerations.
  • Legal Resilience. Maintaining validity requires ongoing vigilance against prior art challenges and proper patent prosecution strategies.
  • Market Impact. Patent EP2451482 offers significant exclusivity, influencing R&D directions and licensing opportunities.

FAQs

1. What is the primary technological innovation of EP2451482?
It involves a novel formulation/method for a specific therapeutic agent aimed at improving efficacy or stability, though exact details depend on the specific claims.

2. How broad are the claims of EP2451482?
The claims likely balance between specificity—covering particular compositions or uses—and broader language to encompass various embodiments, reinforced by dependent claims.

3. Can competitors develop similar drugs without infringing?
Yes, if they design around the specific claims—altering formulations, delivery systems, or therapeutic indications—without crossing the claim scope boundaries.

4. What is the strategic value of patent EP2451482?
It provides exclusive rights that can be leveraged for licensing, partnerships, or blocking competitors, significantly impacting the commercial success of the associated drug.

5. How does patent landscape analysis help in drug development?
It reveals existing protections, potential gaps, and freedom-to-operate constraints, guiding R&D investments and licensing strategies.


References:

  1. European Patent Office. "European Patent EP2451482" — Full Patent Documentation.
  2. WIPO PatentScope. “Patent Family and Related Filings” — National and regional filings.
  3. [1] Confidential patent databases and legal status reports.

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