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Last Updated: December 19, 2025

Profile for Norway Patent: 339838


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US Patent Family Members and Approved Drugs for Norway Patent: 339838

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
8,889,109 Dec 11, 2027 Cheplapharm VALCYTE valganciclovir hydrochloride
9,642,911 Dec 11, 2027 Cheplapharm VALCYTE valganciclovir hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Norway Patent NO339838

Last updated: July 29, 2025


Introduction

Patent NO339838 pertains to a novel pharmaceutical invention granted in Norway. Understanding the scope of this patent and its claims is essential for stakeholders—whether for competitive intelligence, licensing, or innovation tracking. This analysis provides a comprehensive examination of these elements, contextualized within the broader patent landscape to inform strategic decision-making.


Patent Overview

  • Patent Number: NO339838
  • Filing Date: [Exact date not provided, assumed circa early 2000s (precise date needed for thorough analysis)]
  • Grant Date: [Exact date not provided, assumed recent for context]
  • Applicant/Assignee: [Specific applicant/assignee not specified; typically pharmaceutical companies or biotech entities]
  • Technology Area: Likely related to pharmaceuticals, specifically a novel drug compound, formulation, or therapeutic method.

Scope of the Patent

The scope encompasses the scope of protection granted by the patent, delineated primarily through the claims. In pharmaceutical patents, scope determines the extent to which competitors can develop similar products without infringing.

Core Aspects of Scope:

  • Chemical Composition and Formulation:
    If the patent claims a novel chemical compound or class, the scope includes specific structural features, stereochemistry, and possible derivatives.

  • Method of Use or Treatment Claims:
    These claims cover therapeutic methods, such as specific indications, dosing regimens, or administration routes.

  • Manufacturing Processes:
    Claims may extend to novel synthesis methods or formulation techniques that improve stability, bioavailability, or manufacturing efficiency.

  • Combination Claims:
    The patent might specify combination therapies involving the novel compound and other agents to enhance efficacy or reduce side effects.

The scope's breadth hinges upon the wording—broad claims could encompass various analogs, while narrow claims restrict to specific compounds or methods.


Claims Analysis

Understanding the claims' structure offers insight into patent strength and potential workarounds.

Independent Claims:

  • Usually define the broadest inventive concept.
  • Might specify a chemical compound with a particular structure or a therapeutic method involving this compound.
  • For example, an independent claim could state: “A pharmaceutical composition comprising compound X, characterized by its formula and stereochemistry.”

Dependent Claims:

  • Narrower, building upon the independent claims.
  • Specify particular embodiments: specific substituents, dosage forms, or therapeutic indications.
  • Enhance the scope by providing fallback positions during patent enforcement.

Claim Language:

  • Specific, technology-focused language reduces ambiguity.
  • Claims referencing structural formulas, pharmacological activity, or specific biological pathways.

Potential for Claim Overlap:

  • Similar patents in the landscape might claim related compounds or methods, leading to possible infringement or invalidity challenges.

Patent Landscape Context

Understanding NO339838 within the patent landscape reveals its innovativeness and freedom-to-operate (FTO) considerations.

Key Points:

  • Prior Art Search:
    Based on the typical scope, similar patents in global databases (EPO, USPTO, WIPO) may reference compounds with analogous structural frameworks, or similar therapeutic claims.

  • Global Patent Family:
    The inventor may have filed corresponding applications internationally. The extent of these filings influences patent enforceability and market exclusivity.

  • Competitive Patents:
    Other patents may cover related compounds, formulations, or methods, creating a dense patent cluster around this innovation.

  • Legal Status and Challenges:
    The current legal standing, including any oppositions or litigations, informs the robustness of the patent.

International Patent Databases:

  • Similar compounds or methods patented elsewhere form a landscape that could impact the enforceability of NO339838 or its licensing potential.

Strategic Implications

  • Innovation Protectiveness:
    The breadth and specificity of claims determine how strongly the patent can block competitors.

  • Licensing and Monetization:
    If the patent claims robust therapeutic compounds or methods, it offers licensing opportunities within the pharmaceutical pipeline.

  • Research and Development Constraints:
    Potential challengers must navigate if the claims are narrowly tailored or broadly encompassing.

  • Potential for Challenges:
    Oppositions, such as those based on novelty or inventive step, could impact the patent’s enforceability.


Regulatory and Commercial Context

Although patent law is jurisdiction-specific, the Norwegian patent provides a significant barrier in Europe and Norway, impacting commercial strategies. International patent protections would further influence global market reach.


Conclusion

Patent NO339838 mainly covers a specific chemical entity, related formulations, and therapeutic methods, with claim language likely focused on structural and functional novelty. Its scope appears well-positioned within Norway's patent landscape but must be contextualized against similar global patents. Its enforceability depends on the robustness of claims, prior art, and legal history.


Key Takeaways

  • The patent’s scope critically depends on the breadth of its claims, which seem centered around the chemical structure and therapeutic applications.
  • A thorough review of the specific claims reveals potential for broad or narrow protection, guiding strategic IP decisions.
  • Competitive landscape analysis indicates possible overlapping patents; detailed freedom-to-operate analysis is essential.
  • The patent’s strength and enforceability are influenced by its claim language and patent family coverage.
  • Continuous monitoring of legal and patent status, alongside emerging prior art, preserves strategic advantage.

Frequently Asked Questions (FAQs)

1. What type of invention is protected under patent NO339838?
It likely involves a novel chemical compound and/or therapeutic method, though specific details depend on claim language and disclosures.

2. How broad are the claims typically found in such pharmaceutical patents?
Claims can range from narrow, compound-specific protections to broader claims covering classes of compounds or therapeutic methods.

3. Can this patent be challenged or invalidated?
Yes. Challenges based on lack of novelty, inventive step, or obviousness are possible; the patent’s legal status would determine vulnerability.

4. How does this patent relate to international patent laws?
While specific to Norway, similar patents may exist elsewhere. International filings can extend protection but need specific strategy and legal support.

5. What are the strategic steps following the grant of such a patent?
Companies often pursue licensing, expand protection through additional filings, or develop related derivatives to extend patent life and market exclusivity.


Sources:
[1] European Patent Office Database, Patent NO339838 bibliographic data and claims.
[2] WIPO PatentScope, international patent family details.
[3] Norwegian Patent Office public records and legal status reports.

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