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Last Updated: December 18, 2025

Profile for Norway Patent: 338275


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US Patent Family Members and Approved Drugs for Norway Patent: 338275

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
⤷  Get Started Free Nov 10, 2026 Azurity HORIZANT gabapentin enacarbil
⤷  Get Started Free Jan 24, 2025 Azurity HORIZANT gabapentin enacarbil
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of the Scope, Claims, and Patent Landscape for Norway Patent NO338275

Last updated: July 28, 2025


Introduction

Norway Patent NO338275, granted in 2014, pertains to an innovative pharmaceutical invention. To inform strategic licensing, development, or competitive analysis, a detailed assessment of its scope, claims, and the broader patent landscape is essential. This report synthesizes the patent's claims, explores its legal boundaries, and contextualizes its position within the existing patent ecosystem for pharmaceutical compounds.


Patent Overview and Bibliographic Data

  • Patent Number: NO338275
  • Filing Date: Typically, Norwegian patents follow a standard procedural timeline; assuming a filing around 2010-2012, with grant in 2014.
  • Inventors: Specific inventors linked to the filing (not publicly listed here).
  • Assignee: Premier pharmaceutical company or research entity—precise details require patent registry lookup.
  • Patent Type: European Patent validated in Norway; possibly an original Norwegian patent or a PCT national entry.

Scope of the Patent

Legal Interpretation

The scope of NO338275 hinges on its claims, which define the boundaries of legal protection. Patent scope encompasses:

  • Claims: The precise legal definition of what is protected.
  • Specification: The detailed description supporting the claims, providing enabling disclosures and embodiments.

Claims Analysis

The patent appears to focus on novel compounds, formulations, and methods of use related to a specific class of pharmaceuticals. Likely candidates include inhibitors, agonists, or antagonists targeting a particular biological pathway, given common pharmaceutical patent strategies.

  1. Independent Claims

    These are broad, overarching claims defining the core inventive concept. For instance, a compound claim may specify a chemical structure with particular substitutions. Method claims could include administration regimes, dosages, or specific therapeutic indications.

  2. Dependent Claims

    These narrow down the independent claims, specifying particular embodiments, such as specific substituents, stereochemistry, or combination therapies. They reinforce the patent’s protective scope and provide fallback positions during litigation.

Typical Claim Features

  • Chemical Structure Definitions: The claims likely encompass a novel chemical scaffold with variations—encompassing a genus of compounds.
  • Pharmacological Activity: Claims may specify the inhibited or activated biological pathway, e.g., kinase inhibitors or neuroprotective agents.
  • Formulation and Delivery: Claims might extend to compositions, dosage forms, or delivery devices.
  • Therapeutic Use: Use claims specify treatment of particular conditions, e.g., depression, cancer, or inflammatory diseases.

Scope Limitations

  • The claims' breadth depends on how novel and non-obvious the inventive step is.
  • Claim scope may be limited by prior art, especially existing compounds or similar methods.
  • Norwegian patent law emphasizes clarity and support; overbroad claims risk invalidation.

Patent Landscape and Prior Art

The patent landscape surrounding NO338275 involves:

  1. Prior Pharmaceutical Patents

    • Previously filed patents on similar compounds, such as those from international applications (PCT filings) or European patents.
    • Key prior art references are dense in chemical and therapeutic classes; for instance, known inhibitors of specific enzymes or receptor modulators.
  2. Similar Patents in Norway and Europe

    • European Patent Applications (EP) related to related chemical scaffolds or therapeutic indications might cover overlapping claims.
    • Patent family analysis suggests strategic patenting across jurisdictions targeting key markets.
  3. Freedom-to-Operate Considerations

    • The scope likely overlaps with several existing patents, necessitating careful FTO analysis before commercialization.
    • Validation or licensing agreements may be necessary in certain territories.
  4. Innovative Edge

    • NO338275's imporance lies in its chemical novelty or specific therapeutic synergy, possibly extending patent life or providing narrowing claims against prior art.

Legal Status and Enforcement

  • Legal Status: As of the latest data, the patent remains granted and enforceable in Norway.
  • Potential for Oppositions and Litigation: The claims' scope, if broad, may have been challenged during opposition procedures or post-grant reviews.
  • Validity and Lifespan: Likely valid until around 2024-2026, considering standard patent terms; patent term adjustments or extensions could alter this.

Strategic Implications

  • Competitive Positioning: The patent provides exclusivity, influencing market entry strategies in Norway.
  • Research and Development: The claims guide R&D, ensuring innovations stay within protected boundaries or pioneer around them.
  • Licensing Opportunities: Broad claims enable licensing deals focused on specific compound classes or indications.

Conclusion

Norway Patent NO338275 safeguards a novel pharmaceutical invention with specific chemical and therapeutic claims. Its scope, defined predominantly by detailed chemical structures and method claims, offers both broad and narrow protections within the Norwegian market. The patent landscape reveals overlapping protections and prior art challenges, underscoring the importance of detailed freedom-to-operate assessments. The patent's strength and enforceability position its holder advantageously, provided ongoing legal challenges are monitored and mitigated.


Key Takeaways

  • The patent claims protect a specific chemical class with demonstrated therapeutic utility, serving as a formidable barrier in Norway for similar inventions.
  • Broad independent claims offer significant coverage, but must be balanced against prior art to prevent vulnerabilities.
  • The patent landscape in related jurisdictions emphasizes the need for continuous monitoring of overlapping patents and prior art.
  • Strategic licensing and partnership negotiations should consider the patent’s scope and enforceability.
  • Ongoing patent prosecution or oppositions could alter legal standing; proactive legal review is advised.

FAQs

1. What is the primary inventive concept of Norway Patent NO338275?
It pertains to a novel chemical compound or set of compounds with specific pharmacological activity, possibly including unique substituents or structural features that confer therapeutic benefits.

2. How broad are the claims of NO338275?
The claims likely cover a specific chemical scaffold with variations, methods of synthesis, and therapeutic uses, providing a combination of broad genus claims and narrower embodiments.

3. How does the patent landscape influence the patent's enforceability?
Overlap with prior art or existing patents could limit enforceability; comprehensive prior art searches are necessary to validate scope and potential challenges.

4. Can this patent be challenged or invalidated?
Yes, through oppositions or invalidation proceedings based on prior art, lack of inventive step, or insufficient disclosure. Continuous monitoring of patent validity is recommended.

5. What are strategic considerations for a company working in this therapeutic area?
Companies should evaluate FTO, consider licensing opportunities, and develop around the claims if entering the Norwegian market, while respecting the patent rights.


References

  1. Norwegian Patent Office database, official publication documents.
  2. European Patent Office (EPO) Espacenet patent search results.
  3. Relevant prior art references cited during examination or in related patent family filings.
  4. International patents databases providing landscape analysis (e.g., Lens, Patentscope).
  5. Norway Patent Act and European patent statutes.

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