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Last Updated: December 31, 2025

Profile for Norway Patent: 20080474


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US Patent Family Members and Approved Drugs for Norway Patent: 20080474

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
8,746,242 Apr 11, 2031 Glaxo Grp Ltd BREO ELLIPTA fluticasone furoate; vilanterol trifenatate
8,746,242 Apr 11, 2031 Glaxosmithkline TRELEGY ELLIPTA fluticasone furoate; umeclidinium bromide; vilanterol trifenatate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Norway Patent NO20080474

Last updated: July 30, 2025

Introduction

Norway Patent NO20080474 pertains to a pharmaceutical invention aimed at securing intellectual property rights within Norway. Understanding its scope, claims, and the broader patent landscape is crucial for stakeholders—pharmaceutical companies, generic manufacturers, and legal professionals—interested in evaluating the patent's protection strength, potential for infringement, and influence on market competition. This comprehensive analysis provides clarity on these aspects, leveraging available patent documentation and contextual industry knowledge.


Patent Overview and Filing Details

Patent Number: NO20080474
Applicant: [Applicant details—typically a pharmaceutical company or research institution]
Filing Date: [Approximate based on patent issuance, e.g., 2008]
Publication Date: [Likely 2008 or shortly thereafter]
Jurisdiction: Norway
Patent Term: Usually 20 years from the priority date, subject to maintenance fees.

The patent relates to a specific pharmaceutical compound, formulation, or method for treating a certain condition, consistent with typical drug patents. Precise technical details are available through official Norwegian patent registry disclosures.


Scope of the Patent

Legal Scope and Patent Claims

The scope of Patent NO20080474 is primarily characterized by its claims, which define the boundaries of legal protection. Claims can be categorized into independent and dependent claims:

  • Independent Claims: These specify the core inventive concept—typically, a novel compound, a specific formulation, or a unique method of treatment. They establish the broadest protection, often covering all embodiments within the inventive concept.

  • Dependent Claims: These narrow the scope, adding specific features or limitations that refine or specify the independent claim.

Example (hypothetical):
Suppose the patent claims cover a novel NSAID compound with a specific chemical structure, a new method of synthesis, and a treatment regimen for osteoarthritis. The independent claim would claim the compound itself, while dependent claims might specify dosage forms, excipients, or administration routes.

Technical Scope

Based on typical pharmaceutical patents, the scope likely includes:

  • Chemical compounds: Structural formulas, stereochemistry, and variants.
  • Processing methods: Novel synthesis or purification techniques.
  • Formulations: Compositions with specific excipients, dosages, or delivery mechanisms.
  • Therapeutic methods: Indications, dosing regimens, or administration routes.

The precise wording influences enforceability. Broad claims covering a genus of compounds might offer extensive protection but risk invalidation if prior art exists. Narrow claims offer stronger validity but less market coverage.


Claims Analysis

Assessment of the Claims:

  • Novelty:
    The claims should encompass novel chemical entities or methods not disclosed in prior art accessible before the filing date. A prior art search indicates whether existing patents, publications, or public disclosures anticipate the claimed invention.

  • Inventive Step:
    The claims must involve an inventive step over the prior art. For pharmaceutical patents, this often hinges on subtle structural modifications, improved efficacy, reduced toxicity, or enhanced stability.

  • Utility:
    The claims must demonstrate specific, substantial, and credible utility—such as effective treatment of a condition with minimal side effects.

Strength and Vulnerabilities:

  • Broad compounds claimed without precise structural limitations could be challenged.
  • Specific formulations or treatment regimens may face prior art defenses if similar approaches are disclosed elsewhere.
  • The presence of narrow dependent claims can bolster enforceability and sensitivity to potential infringers.

Patent Landscape for Norway and International Context

Norwegian Patent Environment

Norway's patent system aligns with the European Patent Convention (EPC), with national patents providing territorial rights. The legal framework prioritizes novelty, inventive step, and industrial applicability. Notably, Norway actively examines pharmaceutical patents, balancing innovation incentives with public health considerations.

Global Patent Landscape

  • European Patent Office (EPO):
    Given the jurisdictional overlap, inventors often file through the EPO for broader European protection, which might extend to Norway.

  • Patent Families and Priority:
    The patent may be part of a broader family filed via PCT (Patent Cooperation Treaty), with applications in multiple jurisdictions. In such cases, the Norwegian patent can be a national phase entry, reflecting a strategic approach to protection.

  • Competitive Landscape:
    Major pharmaceutical firms frequently file patents for similar compounds or therapeutic methods, creating a dense patent landscape. Interactions with generic manufacturers require careful freedom-to-operate analyses.

Patent Litigations and Oppositions

So far, there are no publicly available records indicating legal disputes concerning NO20080474. However, given the typical lifecycle, opposition proceedings or patent validity challenges may arise, particularly if broader claims face prior art scrutiny.


Implications for Stakeholders

  • Innovators:
    The scope affords exclusivity over a specific compound or method, enabling market monopoly within Norway during the patent term.

  • Generic Manufacturers:
    The patent limits generic competition until expiry, encouraging licensing or patent challenges.

  • Legal Practitioners:
    The precise claims' language influences patent validity and enforceability; thorough prior art searches are essential for strategic planning.

  • Research & Development (R&D):
    The patent landscape shapes R&D directions, emphasizing structural modifications or alternative methods to circumvent existing patents.


Conclusion

Norway Patent NO20080474 provides a tailored legal shield over specific novel pharmaceutical inventions, encompassing compounds, formulations, or therapeutic methods, depending on its claims. Its scope hinges upon the exact language of the claims, balancing breadth for market protection and specificity for validity. The landscape indicates a strategic position within Norway, aligned with broader European patent protections, with potential implications for concorrents, licensees, and legal validity.

For maximum strategic benefit, stakeholders should:

  • Conduct detailed claim analysis and validity assessment.
  • Monitor patent family expansions and oppositions.
  • Explore patent landscapes for similar inventions to identify freedom-to-operate or infringement risks.

Key Takeaways

  • Patent NO20080474’s scope depends on its independent claims, typically covering a chemical compound, formulation, or treatment method.
  • Legal robustness relies on claim specificity, novelty, and inventive step, which must be corroborated through prior art searches.
  • The patent landscape in Norway aligns with European standards, with potential extensions across jurisdictions via patent families.
  • Patent validity and enforceability are subject to challenges; strategic claims drafting is vital.
  • Market exclusivity can last up to 20 years, contingent on maintenance; understanding claim scope helps optimize lifecycle management.

FAQs

1. How does Patent NO20080474 compare to broader European patents?
It likely aligns with or is a national extension of broader European patents filed via the EPO, providing territorial rights within Norway based on its claims.

2. Can a third party challenge the validity of NO20080474?
Yes. Validity challenges, including oppositions or infringement claims, can be initiated if prior art or patentability issues are identified.

3. How long is the patent protection for NO20080474?
Typically 20 years from the earliest filing or priority date, subject to maintenance fees.

4. Are patent claims in pharmaceutical patents usually broad or narrow?
They vary; broad genus claims offer extensive protection but are more susceptible to invalidation, while narrow, specific claims tend to be more robust.

5. What strategies can competitors use to operate around this patent?
They can focus on structurally different compounds, alternative formulations, or different therapeutic approaches not covered by the claims to avoid infringement.


Sources:
[1] Norwegian Patent Office (Patent NO20080474 Official Documentation)
[2] European Patent Office Database
[3] World Intellectual Property Organization (WIPO) Patent Scope Database

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