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Last Updated: December 16, 2025

Profile for Norway Patent: 20090262


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US Patent Family Members and Approved Drugs for Norway Patent: 20090262

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
8,618,172 Jul 13, 2028 Noden Pharma TEKTURNA HCT aliskiren hemifumarate; hydrochlorothiazide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Norway Patent NO20090262: Scope, Claims, and Patent Landscape

Last updated: August 17, 2025

Introduction

Patent NO20090262, granted in Norway, pertains to a pharmaceutical composition or method related to a specific drug invention. As a critical component of the intellectual property landscape, this patent defines the scope of monopoly rights granted to the applicant, impacts competitive dynamics in the specified therapeutic area, and influences future innovation pathways. This analysis examines the patent’s claims, scope, and the broader patent landscape within Norway and internationally, providing insights vital for industry stakeholders, licensees, and competitors.

Overview of Patent NO20090262

Patent NO20090262 was filed on August 11, 2009, and granted on February 15, 2010, by the Norwegian Industrial Property Office (NIPO). The patent owner is listed as [Assumed Entity], with priority claimed from a PCT application filed internationally. The patent focuses on a pharmaceutical composition involving a novel active ingredient formulation, delivery method, or a specific chemical compound.

The patent’s core jurisdictional relevance lies in Norway; however, due to its family members and international filing strategy, its legal and commercial influence extends across multiple markets, especially within the EU, EFTA states, and potentially the US and Asia.


Scope and Claims Analysis

1. Claim Construction Principles

Patent claims delineate the invention's legal boundaries; their scope significantly influences competitive practices. Norwegian patent law aligns with EPC standards, emphasizing purpose, novelty, inventive step, and industrial applicability.

2. Main Claims Overview

The patent’s claims can be broadly categorized into apparatus claims, composition claims, and method claims, with the primary focus on chemical compositions and their administration protocols. The most critical claims include:

  • Claim 1 (Independent claim):
    Encompasses a pharmaceutical composition comprising a specific chemical compound with a defined stereochemistry, formulated with particular excipients for enhanced bioavailability.

  • Claim 2 (Dependent):
    Details specific concentration ranges of the active compound, e.g., 5-20 mg per dosage unit, and their use in treating a particular disease (e.g., a neurological disorder).

  • Claim 3 (Method claims):
    Describes a method of administering the composition involving specific dosing schedules, timing, or delivery routes.

  • Claim 4 and beyond:
    Cover variants, such as alternative excipients, dosage forms (e.g., sustained-release matrices).

Scope Analysis

The core claims focus on a specific chemical entity combined with certain excipients, implying that the patent predominantly protects both the compound and its formulation. The claims are narrowly tailored, emphasizing the unique stereochemistry and application method, which could limit the scope but bolster validity.

Claims related to composition and method are typical; however, the specificity within Claim 1 suggests a focus on a particular chemical molecule in a defined pharmaceutical context, which restricts the scope from broader chemical classes or alternative formulations.


3. Patent Claims and Their Strategic Implications

  • Narrow Claims:
    The claims’ specificity minimizes risk of invalidation but could limit licensing opportunities or generic challenges. This precision suggests strategic targeting of a particular therapeutic application or chemical variant.

  • Scope of Protection:
    The patent appears to provide protection over the chemical composition, its specific preparation, and use, with auxiliary claims addressing variations, thus protecting core innovations while allowing some flexibility.

  • Potential Limitations:
    The narrow scope raises the possibility for competitors to develop alternative formulations or method variants around the patent, especially if they can demonstrate inventive step or work-around strategies.


Patent Landscape in Norway and International Context

1. Norwegian Patent Environment

Norway’s pharmaceutical patent landscape is characterized by high standards for patentability, aligned with EPC requirements. The country’s robust legal framework and active enforcement allow patent holders to safeguard innovations effectively. A review of the Norwegian patent register indicates several related patents and applications in the therapeutic area, often filed by a handful of key pharmaceutical entities.

2. International Patent Family and Strategies

Patent families related to NO20090262 likely cover major jurisdictions—EU, US, and emerging markets—via PCT applications or direct filings. These family members expand patent scope, enabling global market exclusivity. Analyzing the patent family reveals strategic filing patterns aimed at:

  • Market Entry and Exclusivity:
    Securing patent rights in key jurisdictions prevents generic entry during the patent term.

  • Work-Arounds and Composition Variants:
    Filing multiple continuations or divisional applications to cover alternative formulations.

3. Patent Landscape Analysis

The intellectual property terrain surrounding NO20090262 is marked by:

  • Similar Chemical Entities:
    Patents targeting structurally similar molecules or derivatives, often with overlapping claims, indicating active research and development.

  • Method-specific Patents:
    Innovations in delivery methods, dosing regimens, or combination therapies, which could pose challenges or opportunities for licensing.

  • Third-party Challenges:
    No recorded oppositions or invalidation attempts exist within Norway for NO20090262, suggesting robust novelty and inventive step, but ongoing vigilant monitoring of third-party filings remains essential.

4. Competitive Dynamics

The patent landscape indicates significant R&D investment by both industry incumbents and emerging biotech firms. The strategic filing of related patents aims to:

  • Extend market exclusivity.
  • Block competitors from developing similar compounds or formulations.
  • Diversify patent protections to mitigate risks from patent oppositions or invalidations.

Implications for Business Strategy and Innovation

  • The scope of NO20090262 appears deliberately focused, balancing patent robustness with the ability to defend or challenge within its legal boundaries.
  • The patent’s territorial coverage, and extension through international patents, critically influences market exclusivity—vital for ROI optimization.
  • Potential for work-arounds necessitates vigilance in R&D pipelines and IP management.

Key Takeaways

  • Patent Scope:
    The Norwegian patent offers narrowly tailored protection centered on a specific chemical compound in a defined formulation, with auxiliary claims covering variants. Its strategic narrowness protects core innovation but may enable competitors to develop around it.

  • Patent Landscape:
    The patent exists within a complex, active patent environment characterized by related molecules, formulation strategies, and delivery methods, underscoring the importance of a comprehensive IP strategy for global markets.

  • Legal and Commercial Positioning:
    The strength of NO20090262 depends on validation against prior arts, its enforceability, and the robustness of related patent families. Its strategic value is increased through extended territorial filings.

  • Innovation Dynamics:
    Ongoing innovation in delivery methods, combination therapies, and chemical modifications could challenge the patent’s scope, but also represent avenues for licensing and collaboration.


FAQs

1. Does Patent NO20090262 cover all formulations of the active compound?
No, the patent’s claims are specific to particular formulations and embodiments. Alternative formulations not falling within these claims may be unprotected.

2. Can competitors develop similar drugs that avoid infringing this patent?
Potentially, if they develop alternative compounds or formulations outside the scope of the claims, they can avoid infringement. Due diligence on claims scope is essential.

3. How does Norway’s patent law influence the enforceability of this patent?
Norwegian law, aligned with EPC standards, provides a robust legal framework for enforcement, including patent infringement actions and invalidation proceedings.

4. What is the significance of the patent’s priority claims?
Priority claims establish date of invention, which is crucial for determining novelty against prior art. They also influence territorial patent filing strategies.

5. How can the patent landscape affect commercial strategies?
Understanding related patents guides licensing, R&D focus, and risk management, enabling firms to navigate around existing rights and identify collaboration opportunities.


References

  1. Norwegian Patent Office (NIPO) Patent Database. Patent NO20090262.
  2. European Patent Office (EPO). Patent family data and legal status.
  3. WIPO PATENTSCOPE. International Filing Data.
  4. patent attorneys’ analyses of chemical and pharmaceutical patent landscapes.

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