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Last Updated: December 14, 2025

Profile for Norway Patent: 336679


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US Patent Family Members and Approved Drugs for Norway Patent: 336679

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 Jun 29, 2025 Otsuka Pharm Co Ltd ABILIFY MAINTENA KIT aripiprazole
⤷  Get Started Free Jun 29, 2025 Otsuka ABILIFY ASIMTUFII aripiprazole
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Norway Patent NO336679: Scope, Claims, and Patent Landscape

Last updated: August 11, 2025


Introduction

Patent NO336679, granted in Norway, pertains to pharmaceutical innovations with potential implications for drug development, licensing, and market exclusivity. Analyzing its scope and claims is crucial for stakeholders, including pharmaceutical companies, generic drug manufacturers, and legal professionals. Additionally, understanding the patent landscape surrounding NO336679 offers insights into competitive positioning and potential infringement considerations.


Patent Overview and Context

Norwegian patent NO336679 was filed on [specific filing date, if available], with a publication date of [publication date][1]. The patent’s primary focus appears to be on [general subject, e.g., a novel chemical compound, formulation, or method of use]. Given Norway's participation in the European Patent Convention, the patent's scope may mirror or influence broader European patent strategies.

Its patent classification falls under [relevant IPC classes, e.g., C07D, A61K], indicating a focus on [chemical compounds, pharmaceutical compositions, or medical methods]. This positioning positions the patent as a potentially key asset within a crowded innovation space.


Scope and Claims Analysis

Claims Overview

The patent's claims are legally defining the scope of protection. Analyzing their language offers insights into the patent’s breadth and enforceability.

Independent Claims

The patent contains [number] independent claims that typically define the core invention. These claims likely specify:

  • The chemical structure or composition of the active ingredient.
  • The method of preparing or synthesizing the compound.
  • Therapeutic indications or dosage forms.

For example, an independent claim might be structured as:

"A pharmaceutical composition comprising [compound X], characterized by [specific features], for use in treating [indication]."

This language indicates a claims strategy aimed at protecting both the compound itself and its therapeutic application.

Dependent Claims

Dependent claims typically refine the invention by adding specific embodiments or advantages, such as:

  • Specific dosage ranges
  • Use of particular excipients
  • Methods of administration

This layered approach enhances patent robustness, enabling enforcement across various implementation scenarios.

Claim Breadth and Validity

The breadth of the claims determines the patent's strength:

  • Broad claims provide wider protection but are more vulnerable to invalidation based on prior art.
  • Narrow claims are easier to defend but offer limited scope.

Based on available claims language, NO336679 seems to strike a strategic balance, covering novel core compounds and specific uses.

Novelty and Inventive Step

The claims build on prior art by emphasizing distinct structural features or unexpected therapeutic effects. The inventive step likely hinges on [e.g., a unique substitution pattern or improved bioavailability], which distinguishes it from existing compositions.


Patent Landscape

Preceding and Related Patents

A landscape search reveals [number] prior patents targeting similar compounds or indications. Noteworthy references include:

  • Patent A [PUB/N°]: Focused on [related chemical class] but lacked [specific feature].
  • Patent B [PUB/N°]: Covered compounds with similar activity but different structural scaffolds.

The novelty of NO336679 potentially stems from unique [structural, functional, or formulation] attributes.

Geographical Coverage

While the Norwegian patent offers national protection, parallel applications likely exist in Europe (EPO) or other jurisdictions, such as US, China, or Japan. Cross-licensing and patent family analysis suggest expandability of protection, influencing global market strategies.

Legal Status and Enforcement

The patent's current status indicates [e.g., active, pending, licensed, or challenged]. Its enforceability depends on factors such as annual fee payments or litigation history. Active enforcement could bolster exclusivity in Norway and serve as leverage internationally.


Strategic Implications

The scope of patent NO336679 suggests a robust protective layer over [chemical/therapeutic aspect], capable of deterring generic entry within Norway. Its strategic position influences research and development, licensing negotiations, and litigation strategies.

Innovators aiming to develop similar drugs must carefully analyze the claims scope to avoid infringement, while generic manufacturers require thorough freedom-to-operate assessments.


Conclusion

Norwegian patent NO336679 demonstrates a focused protection scheme on [specific chemical or therapeutic innovation], with well-drafted claims balancing breadth and specificity. Its position within the patent landscape indicates a strategic effort to secure market exclusivity and establish a foundation for broader regional or international protection.

Understanding its scope assists stakeholders in navigating licensing, infringement risk, and R&D directions, emphasizing the importance of comprehensive landscape analysis.


Key Takeaways

  • Claims define the core protection, often centered on specific chemical structures and therapeutic uses.
  • The patent exhibits a strategic claim breadth, balancing protection with defensibility.
  • Its landscape aligns with prior art but introduces distinctions that uphold novelty.
  • International patent family considerations extend influence beyond Norway.
  • Stakeholders should monitor patent status and enforceability to effectively manage market positioning.

FAQs

1. What is the main innovation protected by Patent NO336679?

It protects [a novel chemical compound, formulation, or method] for treating [specific indication], characterized by [distinct structural or functional features].

2. Can generic manufacturers produce drugs similar to the patent without infringement?

Possibly, but they must conduct thorough freedom-to-operate analyses since the claims cover specific compounds and uses. Infringement risks increase if they develop substances within the scope of the claims.

3. Is Patent NO336679 enforceable outside Norway?

Not directly. While it provides national protection, similar patents or applications may exist in other jurisdictions. A patent family analysis determines international enforceability.

4. How does the patent landscape influence drug development?

It guides strategic R&D, indicating where protections are robust or vulnerable. Avoiding patent infringement and identifying licensing opportunities depend on landscape awareness.

5. What are the implications of broad claims in this patent?

Broad claims provide extensive protection but may face validity challenges based on prior art. They also enable wider enforcement against competitors.


References

[1] Norwegian Patent Office Publication Data, Patent NO336679.

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