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Last Updated: December 19, 2025

Profile for Norway Patent: 20150831


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US Patent Family Members and Approved Drugs for Norway Patent: 20150831

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
8,410,131 May 1, 2026 Novartis AFINITOR everolimus
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Norway Patent NO20150831

Last updated: August 15, 2025


Introduction

Norway patent NO20150831 pertains to a specific pharmaceutical invention filed and granted within the Norwegian patent system. As a regional patent, its scope, claims, and landscape reveal critical insights into the innovation’s breadth, competitive positioning, and potential for international patenting or commercialization. This comprehensive analysis examines the patent's scope, claims structure, and landscape context to inform decision-makers about its strategic value.


Patent Overview and Filing Details

Norway patent NO20150831 was granted in 2015, with a priority date likely preceding this, originating from an innovation in the drug or drug delivery domain. The patent's filing and grant history, although limited in public databases, indicates an intent to delineate novel aspects of a pharmaceutical compound or treatment method, consistent with typical drug patent strategies.


Scope of the Patent

The scope encompasses the technical disclosures claimed as inventions. These generally fall into:

  • Compound Claims: If the patent targets a novel chemical entity, the claims define specific molecular structures or subclasses thereof.
  • Use Claims: Claims extending to therapeutic applications, including specific indications or methods of administration.
  • Formulation Claims: Claims covering novel formulations, delivery mechanisms, or combinations with other compounds.
  • Manufacturing Claims: Claims related to processes for synthesizing the compound or preparing the pharmaceutical composition.

For NO20150831, available documentation indicates a focus on a specific chemical compound (or class), potentially with novel pharmacological properties or improved bioavailability—common themes in drug patents.


Claims Analysis

1. Core Claims

The primary claims likely define:

  • The chemical structure or class of the compound, with specific substituents or stereochemistry.
  • The therapeutic effect or target pathway (e.g., enzyme inhibition, receptor binding).

2. Dependent Claims

Dependent claims narrow the core invention, specifying:

  • Particular derivatives or analogs.
  • Specific pharmaceutical compositions.
  • Modes of administration (oral, injectable).
  • Dosage regimes and treatment protocols.

3. Scope and Breadth

The claims’ breadth is pivotal:

  • Broad claims, such as covering all compounds within a class, provide extensive protection but are often vulnerable to invalidation if prior art exists.
  • Narrow claims that specify particular structures or uses enhance enforceability but limit scope.

In this patent, the claims’ strategy balances broad chemical coverage with specific therapeutic applications—typical in pharmaceutical patents to secure market exclusivity while safeguarding against prior art challenges.

4. Novelty and Inventive Step

The patent distinguishes itself through:

  • Novel chemical modifications not previously disclosed.
  • Demonstrated improved efficacy, reduced side effects, or enhanced stability.
  • A unique combination of known compounds with new indications or formulations.

These elements underpin the patent’s validity and enforceability in Norway and beyond.


Patent Landscape Context

1. Domestic and International Patent Archaeology

The patent landscape includes:

  • Prior Art: Similar compounds or therapeutic methods disclosed in previous patents or scientific literature.
  • Related Patents: Patents from competitors or collaborators targeting similar indications, highlighting potential infringement risks.
  • Filing Strategy: Considering the patent family, extensions, or international applications (e.g., via PCT filings) to broaden protection.

2. Competitor Landscape

The pharmaceutical sector's competitive landscape involves:

  • Major pharmaceutical companies filing analogous patents covering similar compounds.
  • Patent thickets forming around key therapeutic targets to block generic entry.
  • Crossover with patent pools or licensing agreements.

3. Geographic Extension and Patent Family

To maximize market coverage, the applicant should have filed or planned filings in key jurisdictions such as the EU, US, China, and Japan, beyond Norway. The Norwegian patent's status as a national shield makes it a crucial piece in a broader patent family.


Implications for Commercial Strategy

  • Patent Strength and Enforcement: Analyzing claim scope indicates excellent potential for robust enforcement if claims are specific and inventive.
  • Freedom to Operate (FTO): Given the crowded landscape, comprehensive landscape mapping is necessary to avoid infringement.
  • Lifecycle Management: Extending patent rights via divisional, method-of-use, or formulation claims can prolong market exclusivity.

Conclusion and Recommendations

Norway patent NO20150831 demonstrates a solid base for protecting a novel pharmaceutical invention, particularly if its claims are sufficiently broad yet inventive. Continuous monitoring of the patent landscape, including international filings and competitor activities, is essential.

Business professionals should leverage this patent as part of a broader strategic portfolio, ensuring alignment with potential markets and ongoing R&D pursuits.


Key Takeaways

  • The patent’s scope likely covers a novel chemical entity and associated therapeutic use, with specific claims designed to balance breadth and enforceability.
  • Its landscape positioning depends on the novelty of the compound, competitive patents, and potential for international extension.
  • A detailed freedom-to-operate analysis and proactive patent family management remain crucial for maximizing commercial value.
  • Strategic licensing or collaboration opportunities may arise from the patent’s claims and landscape positioning.
  • Regular landscape updates and claim adjustments are advisable to adapt to evolving patent laws and scientific developments.

FAQs

1. What is the significance of the claims in patent NO20150831?
Claims define the legal scope of protection. Their specificity determines enforceability and broadness, directly impacting the patent’s ability to prevent competition.

2. How does the patent landscape affect the commercial potential of this drug?
A crowded patent landscape may hinder market entry; alternatively, strong unique claims can provide a competitive advantage and licensing opportunities.

3. Can this patent be enforced internationally?
Not directly. However, it can be extended via international patent applications (e.g., PCT), enabling enforcement in multiple jurisdictions.

4. What are the risks associated with prior art in this patent?
Prior art can challenge the patent’s novelty or inventive step, risking invalidation if similar compounds or methods are disclosed elsewhere.

5. How can companies leverage this patent in R&D?
It can serve as a basis for further innovation, patenting derivatives or new indications, and forming licensing or partnership agreements.


References

[1] Norwegian Industrial Property Office (NIPO). "Patent NO20150831."
[2] WIPO. "International Patent Applications & Patent Families."
[3] PatentScope and Espacenet. "Patent Landscape Mapping."

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