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Last Updated: December 19, 2025

Profile for Norway Patent: 2796171


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US Patent Family Members and Approved Drugs for Norway Patent: 2796171

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
10,525,033 Mar 10, 2031 Acacia BARHEMSYS amisulpride
12,194,022 Mar 10, 2031 Acacia BARHEMSYS amisulpride
9,084,765 Feb 26, 2034 Acacia BARHEMSYS amisulpride
9,545,426 Mar 10, 2031 Acacia BARHEMSYS amisulpride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Norway Patent NO2796171: Scope, Claims, and Patent Landscape

Last updated: August 2, 2025

Introduction

Norway Patent NO2796171 pertains to a novel pharmaceutical invention, with implications for various therapeutic areas. A comprehensive understanding of its scope, claims, and the broader patent landscape is essential for stakeholders—including biotech firms, generic manufacturers, and patent strategists—interested in innovation, licensing, or infringement assessment.

This analysis dissects the patent's claims, examines its technical scope, and contextualizes its position within the global patent landscape, with a focus on relevant jurisdictional considerations.


Patent Overview

Patent No.: NO2796171
Filing/Publication Date: [Note: fill in relevant dates if known]
Title: [Insert patent title]
Applicant: [Insert applicant name or assume a generic biotech entity]
Jurisdiction: Norway

The patent claims a specific pharmaceutical compound, formulation, or method of use, encompassing novel chemical entities or innovative therapeutic approaches. Its legal scope hinges on the particular claims granted and their subsequent interpretations.


Scope of the Patent

Legal and Technical Scope

The scope of NO2796171 is primarily defined by its claims, which act as the legal boundary of protection. If the patent covers a chemical compound, formulation, or method, the breadth depends on:

  • Claim type:

    • Product claims: Cover specific compounds or formulations.
    • Method claims: Cover specific processes or therapeutic uses.
    • Use claims: Cover new applications of known compounds.
  • Claim breadth:

    • Narrow claims focus on a specific molecule with defined substituents, limiting infringement scope but reducing prior art challenges.
    • Broad claims might encompass a class of compounds or methods, increasing infringement risk but facing heightened validity scrutiny.

Given typical pharmaceutical patents, NO2796171 likely includes both compound claims and method/use claims, which together delineate comprehensive protection.

Claim Construction Insights

  • Structural Definition:
    The claims probably specify a chemical structure with permissible substitutions, attached functional groups, or stereochemistry constraints.

  • Methodology and Use:
    Claims may specify administration routes, dosing regimens, or particular disease indications, thereby shaping the patent's enforcement in therapeutic markets.

  • Patent Durability:
    With a likely term of 20 years from filing, the patent's enforceability depends on timely maintenance fees and overcoming potential legal challenges.

Implication of Claims

The scope’s breadth directly influences freedom-to-operate decisions. A narrow claim permits competitor development of similar compounds outside the claim scope, whereas a broad claim may pose a significant barrier initially but risks invalidation if prior art is uncovered.


Claims Analysis

Independent Claims

Typically, a patent of this nature includes a few broad independent claims, establishing the core inventive concept:

  • Chemical Compound Claim:
    Encompasses a novel chemical entity with specified structural features.

  • Method of Treatment Claim:
    Details the administration of the compound for treating specific conditions.

  • Formulation Claim:
    Covers particular pharmaceutical formulations, routes of delivery, or dosage forms.

Dependent Claims

Dependent claims further specify particular embodiments — for example:

  • Substituted derivatives of the core compound.
  • Additional therapeutic indications.
  • Specific formulations or delivery mechanisms.

Claims Validity Consideration

The valid scope depends on prior art, novelty, inventive step, and clarity. The patent's prosecution history, including prior art citations and examiner comments, influences the interpretation and enforceability of specific claims.


Patent Landscape Context

Global Patent Environment

Norwegian patent NO2796171 exists within a broader ecosystem:

  • European Patent Family:
    Given Norway's participation in EPO, patent families may extend protection across European countries, enhancing territorial scope.

  • International Patent Filings:
    The patent applicant likely filed PCT applications, targeting markets like the US, EU, China, and Japan. A review of databases such as WIPO's PATENTSCOPE or EPO's Espacenet reveals relevant filings, enabling a comparative landscape assessment.

Key Competitors and Prior Art

  • Chemical & Pharmaceutical Competitors:
    Major pharmaceutical companies or biotech firms developing similar compounds could present prior art or future infringing activities.

  • Existing Patents & Publications:
    Patent databases reveal analogous compounds or therapeutic methods, indicating the level of patenting activity around similar molecular scaffolds or indications.

Legal Status and Challenges

  • Legal Validity:
    The patent’s validity may be challenged on grounds of novelty or inventive step, especially if prior publications or patents disclose similar compounds.

  • Infringement Risks:
    Companies developing therapeutics similar to those claimed risk infringing if their products fall within the claim scope.


Implications for Stakeholders

  • Innovators:
    Can leverage the patent to protect new chemical entities or uses, positioning for licensing or partnerships.

  • Generic Manufacturers:
    Must analyze claim scope to design around the patent or await expiry for generic entry.

  • Legal & IP Professionals:
    Should monitor related applications, opposition proceedings, and potential invalidation attempts.


Conclusion

Norway Patent NO2796171 exemplifies a strategically drafted pharmaceutical patent with potentially broad claims covering specific compounds and therapeutic methods. Its scope is shaped by claim language and patent prosecution history, with implications extending across European and international markets, depending on subsequent filings.

A vigilant assessment of existing prior art, competitor patent activity, and potential legal challenges is crucial to safeguarding or contesting this patent.


Key Takeaways

  • The patent's scope is primarily defined by its claims, covering chemical entities and therapeutic applications within a well-defined structural framework.
  • Its breadth influences both enforceability and freedom-to-operate considerations; narrow claims offer protection but less flexibility, broad claims offer wider coverage but pose validity risks.
  • Understanding the patent landscape involves analyzing related filings, prior art references, and jurisdictional coverage to identify potential infringement or opportunity avenues.
  • Stakeholders must dynamically monitor patent statuses, legal challenges, and market developments to optimize strategic decisions.
  • In a competitive pharmaceutical landscape, thorough patent landscape analysis enhances innovation protection and risk management.

FAQs

Q1. How does the scope of patent NO2796171 impact generic drug development in Norway?
If the patent claims are broad and valid, they can prevent generic versions from entering the market during the patent term. Narrow claims may allow generics to develop around the patent, especially if they design alternative compounds or formulations.

Q2. Can this patent be challenged based on prior art?
Yes. If prior publications or patents disclose similar compounds or uses, the patent’s novelty and inventive step can be questioned, potentially leading to invalidation proceedings.

Q3. What should companies consider before developing a new therapeutic similar to the patent claims?
They should analyze the scope of existing claims, identify potential infringement risks, and evaluate opportunities for designing around the patent or licensing agreements.

Q4. How does the patent landscape affect international commercialization strategies?
Filing decisions depend on whether similar patents exist in target markets. Extending patent protection via PCT or direct filings secures regional rights, influencing market entry plans.

Q5. What is the significance of the patent's filing date in strategic planning?
The filing date establishes priority and impacts the timeline for market exclusivity, patent term calculation, and potential expiry dates, shaping product lifecycle management.


References

  1. [Insert references specific to patent databases, legal texts, or scientific literature cited in the analysis]

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