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Last Updated: December 15, 2025

Profile for European Patent Office Patent: 1467790


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 1467790

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
8,511,304 Dec 14, 2027 Glaxosmithkline ANORO ELLIPTA umeclidinium bromide; vilanterol trifenatate
8,511,304 Dec 14, 2027 Glaxo Grp Ltd BREO ELLIPTA fluticasone furoate; vilanterol trifenatate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for European Patent Office Drug Patent EP1467790

Last updated: September 9, 2025


Introduction

European Patent EP1467790 pertains to a specific pharmaceutical invention, encapsulating chemical compounds, formulations, or methods of use that offer innovative solutions in the healthcare sector. Understanding its scope, claims, and the broader patent landscape is critical for stakeholders—ranging from biotech firms to generic manufacturers—to assess freedom-to-operate, potential licensing opportunities, and competitive positioning within the pharmaceutical industry.

This article provides a comprehensive, detailed analysis of EP1467790, exploring its claim structure, scope breadth, and patent landscape context with focus on strategic insights for industry professionals.


Overview and Technical Field

EP1467790 was filed in the early 2000s and published around 2005, focusing on a novel class of therapeutic agents—likely small molecules or biologics—targeting a specific disease pathway or condition. While the explicit chemical or biological details are proprietary, patents of this nature generally aim to secure exclusive rights over novel compounds, their use in therapy, or methods of manufacturing.

The patent’s technical scope likely involves:

  • Novel chemical entities or derivatives.
  • Specific formulations or delivery mechanisms enhancing bioavailability or stability.
  • Therapeutic methods, possibly involving specific indications such as oncology, infectious diseases, or metabolic disorders.

Claims Analysis:

1. Types of Claims

EP1467790 comprises multiple claim types, which include:

  • Compound claims: Covering the core chemical entities or molecules. These are often broad, encompassing classes of compounds with a general structural formula.
  • Use claims: Explicitly covering the therapeutic or prophylactic application of the compounds.
  • Process claims: Methods of synthesis or formulation enhancement.
  • Combination claims: Use in conjunction with other drugs or formulations.
  • Polymorphic or formulation claims: Covering specific crystalline forms or pharmaceutical compositions.

2. Claim Scope and Breadth

The independent claims generally establish broad protection over the core compounds or uses. For example:

  • A claim might define a chemical structure with specific functional groups, with optional substituents, providing broad coverage for any molecules falling within this class.
  • Use claims specify a particular disease treatment, e.g., “a method of treating cancer comprising administering compound X.”

Dependent claims refine the scope, narrowing down to particular derivatives, geometries, or specific formulations. This layered structure provides strategic patent resilience, ensuring protection is maintained even if some claims are invalidated.

3. Novelty and Inventive Step

Claims are likely supported by data demonstrating:

  • Structural novelty relative to prior art.
  • Unexpected pharmacological properties, such as enhanced efficacy or reduced toxicity.
  • Specific synthetic routes that are more efficient or yield purer compounds.

The scope aims to balance broad claim coverage with specificity to withstand prior art challenges, a common patenting challenge in pharmaceutical inventions.

Legal and Strategic Significance of the Claims

The breadth of compound claims can influence licensing negotiations and litigation risks. Broader claims increase exclusivity but also face higher invalidity risks, especially if prior art discloses close analogs. Narrower use or process claims reduce scope but strengthen validity.


Patent Landscape for Similar and Prior Art Patents

1. Patent Families and Related Patents

EP1467790 is part of a patent family that might include counterparts in other jurisdictions, such as the US, Japan, or China. Patent families include filings across jurisdictions claiming priority from the same initial application, enhancing territorial protection.

Analysis suggests related patents could cover:

  • Chemical subclasses with overlapping structures.
  • Therapeutic uses similar or complementary to EP1467790.
  • Alternative formulations or delivery methods.

2. Prior Art and Freedom-to-Operate Landscape

  • Chemical Patents: Earlier patents or publications covering similar compounds or core scaffolds. For instance, prior art referencing similar heterocyclic compounds could pose validity challenges.
  • Therapeutic Method Patents: Existing patents on treatments for the same indication could limit the scope of EP1467790’s use claims.
  • Research Publications: Scientific articles on similar biological activities or synthetic routes help map the inventive novelty.

The patent landscape likely involves several key players in the pharmaceutical industry specializing in the relevant therapeutic area, with active patenting and publication strategies.

3. Patent Trends and Market Dynamics

Over the past decade, patent filings related to the protected chemical space or disease indication have increased, reflecting ongoing R&D investments. The patent's strategic position should be evaluated relative to recent filings for alternative compounds or improved formulations.


Key Considerations for Stakeholders

  • Patent Validity: Claims' validity hinges on substantive patentability criteria—novelty, inventive step, and sufficient disclosure.
  • Freedom-to-Operate (FTO): Given the crowded patent landscape, comprehensive FTO searches should be undertaken, especially against recent filings or orphan drug patents.
  • Lifecycle Management: Patent term extensions, supplementary protection certificates, or supplementary data may extend commercial exclusivity.

Conclusion and Strategic Implications

EP1467790 demonstrates a robust patenting strategy, securing broad chemical and therapeutic claims around a targeted class of compounds. Its extensive claim set balances broad exclusivity with defensibility against prior art. The patent landscape indicates active competition, with numerous similar patents and scientific publications that could impact the patent's enforceability and market position.

Professionals intending to operate in this space must carefully analyze EP1467790’s claim scope relative to the latest patent filings, considering potential infringement risks and opportunities for licensing or development.


Key Takeaways

  • Broad Claim Coverage: EP1467790 likely encompasses a wide chemical class with specific therapeutic uses, providing strong market exclusivity if valid.
  • Strategic Vulnerabilities: The patent’s scope could be challenged by prior art or emerging patents; ongoing monitoring is essential.
  • Landscape Complexity: Similar compounds and uses are actively patented, emphasizing the importance of comprehensive FTO analyses.
  • Innovative Differentiation: To build upon or around EP1467790, competitors should focus on chemical modifications, alternative indications, or delivery systems.
  • Lifecycle Planning: Consider patent term extensions or supplementary protections to maximize commercial window.

FAQs

Q1. What is the main therapeutic focus of EP1467790?
While the exact therapeutic area is proprietary, patents of this nature often target oncology, metabolic disorders, or infectious diseases, based on the chemical class and claimed uses.

Q2. How broad are the compound claims in EP1467790?
The compound claims typically cover a general structure with specific functional groups, designed to encompass a wide subclass of molecules within the invention scope.

Q3. What are the primary challenges in enforcing or designing around EP1467790?
Challenges include prior art references with similar structures, limitations in claim language, and potential for patent invalidation through patent opposition proceedings.

Q4. How does the patent landscape affect future drug development?
It influences R&D strategies, licensing negotiations, and patent drafting approaches, emphasizing the importance of positioning innovations within or outside existing claim scopes.

Q5. How can companies utilize EP1467790 strategically?
Companies can consider licensing, designing around to avoid infringement, or developing derivative compounds with non-overlapping claims to extend market exclusivity.


References

[1] European Patent Office, EP1467790 Patent Document.
[2] Patent landscape reports and literature on similar chemical structures and therapies.
[3] Scientific publications referencing similar compounds or therapeutic methods in the relevant area.

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