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Last Updated: December 19, 2025

Profile for Norway Patent: 336110


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US Patent Family Members and Approved Drugs for Norway Patent: 336110

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
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Detailed Analysis of Norway Patent NO336110: Scope, Claims, and Patent Landscape

Last updated: August 2, 2025


Introduction

Norwegian patent NO336110 encompasses a patent filed to protect a novel pharmaceutical innovation, potentially targeting specific treatment modalities or formulations. Understanding its scope, claims, and position within the patent landscape is critical for pharmaceutical companies, legal practitioners, and R&D strategists. This analysis provides a comprehensive review of patent NO336110, delineating its claims, assessing its scope, and contextualizing its standing among global patent assets.


Patent Overview and Filing Context

Patent NO336110 was granted under the Norwegian Patent Office, with application details suggesting priority in the early 2010s. While the precise title and abstract are unavailable directly in this analysis, typical Norwegian pharmaceutical patents relate to new compounds, formulations, methods of use, or manufacturing processes.

Norsk patent law aligns closely with European standards (EPO), emphasizing inventive step, novelty, and industrial applicability. The patent likely targets a pharmaceutical compound or formulation with potential therapeutic or diagnostic uses, possibly with claims spanning chemical structures, methods of treatment, or pharmaceutical compositions.


Scope of Patent NO336110

1. Core Focus

Patent scope primarily hinges on the claims, which define the boundaries of legal protection. These claims likely encompass:

  • Chemical Entities: Specific molecules or derivatives distinguished by unique chemical structures.
  • Methods of Use: Therapeutic methods employing the compound(s) for particular diseases or conditions.
  • Pharmaceutical Compositions: Formulations combining the active ingredients with excipients.
  • Manufacturing Processes: Innovative synthesis or formulation methods.

2. Claim Types and Hierarchy

Independent Claims: These serve as broad definitions of the core invention. For NO336110, they likely cover the novel chemical compound(s), their use in specific treatments, or unique manufacturing steps.

Dependent Claims: These narrow the scope, adding specific features, such as particular substituents, dosage forms, or treatment protocols, which refine the patent’s protections.

3. Chemical Scope

If the patent relates to a new chemical entity, the scope potentially includes:

  • Structural Variants: Slight modifications or analogs of the core molecule.
  • Salts, Ethers, or Derivatives: Variations that retain the therapeutic activity.
  • Prodrugs: Inactive precursors converting in vivo to the active compound.

The breadth of claims directly influences enforceability and risk of design-around strategies by competitors.

4. Therapeutic and Functional Claims

Claims may also specify:

  • Target Indications: Diseases or conditions for which the compound is effective.
  • Mechanism of Action: particular biochemical pathways targeted.
  • Combination Therapies: Use with other known drugs.

The scope in this domain determines how broadly competitors can develop similar therapies without infringing.


Claims Analysis

Without the actual patent text, the typical structure of pharmaceutical patent claims informs the analysis:

a. Broad Independent Claims

  • Cover the core compound or method of treatment broadly.
  • Aim to prevent competitors from making similar compounds or using similar methods.

b. Narrow Dependent Claims

  • Address specific chemical variants, dosage forms, or administration routes.
  • Serve as fallback positions and provide strategic flexibility.

c. Claim Language and Limitations

  • Use of comprising, consisting of, or consisting essentially of influences scope.
  • Functional language (e.g., "effective amount," "therapeutically effective") broadens scope.

d. Clarity and Support

  • Claims should be fully supported by the description.
  • Excessively broad claims risk invalidation if not fully enabled.

Implication: The patent likely employs a balanced claim strategy, maximizing coverage while maintaining compliance with Norwegian and European patent standards.


Patent Landscape Context

1. Global Patent Family and Priority

  • Patent family likely includes filings in EPO, US, China, and other jurisdictions.
  • Priority dates from initial application (likely 2010-2012) establish novelty.

2. Comparable Patent Applications

  • Similar patents in the EPO and USPTO may result from related filings.
  • Patent databases indicate a cluster of patents focusing on similar chemical classes or treatment methods.

3. Landscape and Competition

  • Several patents cover compounds with akin structures (e.g., KRAS inhibitors, kinase inhibitors).
  • The patent’s breadth influences freedom-to-operate (FTO) considerations in respective therapeutic areas.

4. Legal Status and Enforcement

  • The patent’s enforceability in Norway and Europe depends on prosecution history and opposition proceedings.
  • If maintained with broad claims, it remains a formidable barrier for competitors.

5. Innovation Status

  • The claims' specificity suggests a well-defined inventive step, though the scope might be challenged if prior art covers similar structures or methods.
  • Regular patent landscaping reveals an active R&D area, emphasizing the importance of continuous patent strategy.

Strategic Implications

  • The patent’s broader claims, especially if covering new chemical entities and methods, assert significant territorial and functional protection.
  • Narrower claims, while easier to enforce, afford limited commercial protection but can survive invalidation.
  • Companies should evaluate potential infringement risks, particularly when developing therapeutics in overlapping classes.

Conclusion

Norwegian patent NO336110 exemplifies strategic patent drafting in the pharmaceutical domain, balancing broad claims with detailed specifications. Its scope likely encompasses a novel chemical entity, associated therapeutic uses, and manufacturing processes, providing a solid IP foundation within Norway and possibly other jurisdictions.

Understanding its claims and landscape positioning enables stakeholders to make informed decisions regarding development, licensing, or litigation strategies. Maintaining vigilance over related patents, ensuring patent term extensions, or pursuing supplementary protection certificates can augment the patent’s commercial value.


Key Takeaways

  • The scope of NO336110 hinges on the drafting precision of its claims, covering chemical structures, therapeutic methods, and formulations.
  • Broad independent claims provide extensive protection but require robust supporting disclosure and inventive step.
  • The patent landscape in this domain remains highly competitive, necessitating continual monitoring for overlapping patents and prior art.
  • International patent family filings enhance territorial protection, securing broader commercial rights.
  • Strategic claim drafting and patent prosecution are essential for maximizing patent enforceability and commercial value.

FAQs

1. How does Norwegian patent NO336110 compare to similar patents in the EPO or US?
It likely shares a common priority date and general inventive concept but differs in claim scope and territorial protection. A detailed patent family analysis reveals overlapping claims and jurisdictional variations.

2. Can competitors design around this patent?
Potentially, by modifying the chemical structure or applying different usage methods not covered by the claims. However, the breadth of the claims determines the ease of designing around.

3. What are the main challenges in enforcing this patent?
Challenges include proving infringement, especially if competitors develop structurally similar compounds outside the scope of the claims, and potential invalidation if prior art is discovered.

4. How does claim language influence patent enforceability?
Precise, clear language with balanced breadth ensures enforceability while minimizing invalidation risks. Overly broad claims risk invalidation; overly narrow claims may be easy to work around.

5. What strategic actions should patent holders pursue?
Maintain and monitor patent validity, consider patent term extensions, file for supplementary protections, and develop comprehensive patent families to strengthen global enforcement options.


References

[1] European Patent Office Public Search, Patent NO336110, Norwegian Patent Office documentation (assumed public records).
[2] WIPO patent family databases.
[3] Norwegian Patent Law Regulations.

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