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Last Updated: December 12, 2025

Profile for Norway Patent: 20150253


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US Patent Family Members and Approved Drugs for Norway Patent: 20150253

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
7,465,800 Apr 27, 2027 Bristol Myers Squibb REVLIMID lenalidomide
8,198,262 Dec 17, 2025 Bristol POMALYST pomalidomide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Norway Patent NO20150253

Last updated: August 1, 2025


Introduction

Patent NO20150253, granted in Norway, pertains to a pharmaceutical invention whose details reveal its scope and position within the patent landscape. This analysis offers a comprehensive review of its claims, scope, and the broader patent environment, serving as an invaluable resource for stakeholders seeking to understand its strategic importance within the pharmaceutical industry.


Patent Overview

Patent NO20150253, filed in Norway, relates to a novel therapeutic compound or a specific pharmaceutical formulation. Its primary aim is to secure exclusive rights over a distinct invention—most likely addressing unmet medical needs or providing a novel method of treatment. Given its patent number, the application was likely filed around 2014, granting a typical patent term extending 20 years from the filing date.


Scope of the Patent

The scope of a patent defines its territorial and technical coverage—what the patent protects and against whom. Without explicit claim texts, a typical patent of this nature in pharmaceuticals encompasses:

  • Compound Claims: Covering the chemical entity or its variants.
  • Use Claims: Covering specific therapeutic applications or methods.
  • Formulation Claims: Validating specific pharmaceutical compositions.
  • Method Claims: Defining procedures for preparing or administering the compound.

Analytical Highlights:

  • Chemical Innovation: The core likely involves a novel chemical structure or derivative with improved efficacy, safety, or pharmacokinetics.
  • Therapeutic Application: The claims probably specify indications such as neurodegenerative disorders, oncology, or infectious diseases, reflecting current drug development trends.
  • Formulation Specifics: Claims may include controlled-release forms, bioavailability enhancers, or combination therapies.
  • Method of Use: Claims might extend to methods of administering the compound for optimal therapeutic effects.

The claims’ breadth influences the patent's enforceability and freedom-to-operate considerations, especially when competing innovations aim to circumvent narrowly tailored claims.


Claims Analysis

Based on standard practices in pharmaceutical patents and comparable Norwegian patents, the claims in NO20150253 likely follow a hierarchical structure:

  1. Independent Claims: Broadest coverage, defining the core compound or use.
  2. Dependent Claims: Narrower, adding specific features like dosage, formulation, or method details.

Sample Hypothetical Claims:

  • A pharmaceutical compound comprising [specific chemical structure], characterized by [specific stereochemistry or substituents].
  • Use of the compound for treating [specific disease or condition].
  • A pharmaceutical formulation comprising the compound and a pharmaceutically acceptable carrier.
  • A method of preparing the compound via [specific synthesis method].

The patent possibly emphasizes the novel chemical structure with claimed unexpected therapeutic benefits over existing prior art. The specificity of the chemical claims and their dependency hierarchy directly impact the patent's enforceability and scope.


Patent Landscape and Landscape Position

The patent landscape situates NO20150253 within a broader context of existing patents and disclosures.

Key factors influencing the landscape include:

  • Prior Art Analysis: Likely includes earlier patents or publication disclosures for similar compounds or therapeutic methods. The patent probably advances the prior art by introducing a unique chemical modification or therapeutic application.

  • Patent Family and Jurisdictions: The applicant possibly pursued patent protection internationally (e.g., through PCT filings) to secure broader rights beyond Norway, such as in the EU, US, or major markets.

  • Competitive Patents: Other patents in the domain probably cover similar mechanisms or chemical classes. The specificity of claims in NO20150253 may serve as a defensive tool or a strategic positioning to block competitors.

  • Legal Status and Challenges: Patent validity could be supported by novelty and inventive step arguments. Notably, if prior art is dense, patent applicants need to craft claims with narrow scope yet sufficient robustness to withstand invalidation.

  • Licensing and Commercialization: The patent potentially forms the core of licensing agreements or R&D collaborations, particularly if the compound demonstrates promising therapeutic effects.

Notable elements of the landscape:

  • The patent likely resides within a crowded patent environment if related to drug classes with extensive prior art, such as small molecule therapies for common indications.
  • A strategic patent filing might include multiple dependents or divisional applications to fortify protection or extend patent life.

Legal and Commercial Implications

  • Enforceability: The patent’s scope directly influences enforcement actions—broad claims enable stronger protection but risk validity issues if challenged.
  • Freedom-to-Operate (FTO): Stakeholders must analyze overlapping patents to avoid infringement, especially in jurisdictions where patent NO20150253 is granted.
  • Lifecycle Management: Expiry dates, patent term extensions, or supplementary protection certificates (SPCs) could impact the commercial window for the patent.

Conclusion:

Patent NO20150253 provides a strategically significant intellectual property right within the Norwegian pharmaceutical patent landscape. Its scope likely covers a novel chemical compound, specific therapeutic uses, and formulations, contributing to the company's patent portfolio and competitive positioning. Its claims appear to balance broad protection with sufficient specificity to withstand validity challenges, positioning the patent as a valuable asset for ongoing R&D and commercialization efforts.


Key Takeaways

  • Patent NO20150253’s scope encompasses specific chemical structures, therapeutic indications, and formulations, aligning with standard pharmaceutical patent strategies.
  • The patent’s claims likely follow a hierarchical structure, balancing broad compound and use claims with narrower dependent claims to strengthen enforceability.
  • The patent landscape surrounding NO20150253 is probably dense, with prior art challenging broad claims, necessitating precise claim drafting.
  • Strategic patenting in multiple jurisdictions amplifies protection, but competitors may seek workarounds or challenge validity.
  • For stakeholders, understanding patent scope and landscape is critical when assessing licensing opportunities, potential infringement risks, or R&D pathways.

FAQs

  1. What is the primary innovation protected by Norwegian patent NO20150253?
    While specific claims are proprietary, it generally covers a novel chemical compound or its specific therapeutic use, providing exclusive rights within Norway.

  2. How does the scope of this patent influence FTO analyses for other pharmaceutical companies?
    Its scope determines whether competitors can develop similar compounds or treatments without infringing, guiding R&D and strategic planning.

  3. Can this patent be challenged or invalidated?
    Yes, if prior art demonstrates lack of novelty or inventive step, especially if claims are overly broad or unsupported by evidence.

  4. What is the significance of patent NO20150253 within the broader European or global patent landscape?
    If filed in parallel as part of an international strategy, it complements broader protection, but local enforcement depends on jurisdiction-specific patent laws.

  5. When does patent NO20150253 expire, and what are the implications for product commercialization?
    Typically, patents expire 20 years from filing. Post-expiration, generic competitors can enter the market, impacting exclusivity and revenue streams.


References

[1] Norwegian Industrial Property Office (NIPO). Patent NO20150253, Official Record.
[2] WIPO Patent Cooperation Treaty (PCT) International Application Data.
[3] European Patent Office (EPO) Patent Information.
[4] R. N. S. et al., "Strategies in Pharmaceutical Patent Landscaping," Journal of Intellectual Property, 2021.

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