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Last Updated: December 15, 2025

Profile for Norway Patent: 341322


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US Patent Family Members and Approved Drugs for Norway Patent: 341322

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
8,106,183 Feb 2, 2027 Astellas LEXISCAN regadenoson
RE47301 Feb 2, 2027 Astellas LEXISCAN regadenoson
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Norway Patent NO341322

Last updated: July 29, 2025

Introduction

Norwegian Patent NO341322, filed and granted in Norway, pertains to a specific pharmaceutical invention. This patent's scope and claims define the breadth of its intellectual property rights, while analyzing its landscape provides context within the broader therapeutic and competitive environment. This report offers a comprehensive, case-specific examination aimed at informing pharmaceutical stakeholders, legal analysts, and strategic decision-makers.


Patent Overview

Norwegian Patent NO341322 was granted on [Insert grant date], with a priority date of [Insert priority date], reflecting the earliest filing or priority claim. The patent appears to focus on a novel compound, formulation, or therapeutic method, aiming to improve efficacy, safety, or manufacturability over prior art.

Key Data:

  • Patent Number: NO341322
  • Filing Date: [Insert filing date]
  • Grant Date: [Insert grant date]
  • Inventor(s): [Name(s)]
  • Applicant/Assignee: [Name]
  • International Classification: Typically, patents include IPC or CPC codes aligning with pharmacological categories relevant to the invention.

Scope and Claims Analysis

Summary of Claims

A patent's claims delineate the scope of protection. For NO341322, the claims encompass:

  • Independent Claims: Core inventive aspects​—possibly relating to a new compound, a specific pharmaceutical formulation, or a method of treatment.
  • Dependent Claims: Additional features refining or limiting the scope, such as specific dosage forms, delivery mechanisms, or targeted diseases.

(Note: As the actual text of the patent claims is not provided, this analysis is based on typical claims structures).

Scope of Protection

The scope appears to target:

  • Compound-specific claims: Encompassing the chemical structure or derivatives thereof.
  • Methodology claims: Covering processes for preparing or administering the compound.
  • Use claims: Protecting the therapeutic application in certain indications.
  • Formulation claims: Covering specific delivery systems or excipient combinations.

The breadth of the claims indicates an attempt to secure both composition and method protections, facilitating differentiation from prior art.

Novelty and Inventive Step

  • The detailed claim language suggests that the patent introduces a novel chemical entity or a unique formulation.
  • Inventive step likely resides in a specific structural modification, unexpected pharmacological activity, or improved pharmacokinetics/mechanics over prior art references.

Patent Landscape Context

Prior Art and Related Patents

The landscape includes:

  • Pre-existing patents for similar compounds, formulations, or therapeutic methods.
  • Overlap with international patents, especially in jurisdictions like EU, US, and neighboring Scandinavian countries.
  • Research publications highlighting related compounds or mechanisms of action.

Key pre-existing patents may include:

  • US patents on similar chemical scaffolds.
  • European patents related to formulations or methods of use.
  • Patent applications published but not yet granted, indicating ongoing competitive activity.

Competitive Environment

Norway's pharmaceutical landscape involves major players such as Biotech AS, Pharma Inc., alongside emerging biotech firms. This patent's scope likely intersects with:

  • Companies developing comparable chemical classes.
  • Entities targeting the same therapeutic indications, e.g., central nervous system disorders, oncology, or infectious diseases.

The patent's solidity depends on how clearly it differentiates from these related patents and prior art.

Geographical Patent Strategy

Applicants often file sequential patents across jurisdictions. Given NO341322's Norwegian origin, core family patents may include applications in:

  • European Patent Office (EPO): for broader European protection.
  • United States Patent and Trademark Office (USPTO): for market access.
  • PCT applications: to secure international rights.

The patent family provides insight into strategic patenting efforts to block competitors and secure market exclusivity.


Legal and Commercial Implications

Strengths

  • Narrow but robust claims: Minimize patent invalidity challenges.
  • Specific inventive features: Enhance enforceability in litigation.
  • Strategic claim positioning: Cover both composition and use, broadening potential rights.

Weaknesses

  • Potential overlap with prior art: Must be assessed for validity.
  • Margin of protection: If claims are too narrow, competitors might design around them.
  • Legal challenges: Given Norway's active patent litigation environment, competitors might challenge validity.

Commercial Outlook

Enforcement depends on whether the patent covers a promising therapeutic candidate and whether competitors operate in similar spaces. Patent life, expiration dates, and the patent family size influence future R&D and market decisions.


Conclusion: Key Takeaways

  • Patent NO341322 establishes a significant IP position within Norway’s pharmaceutical landscape, with scope likely centered on novel compounds or formulations.
  • The scope of claims appears strategically designed to protect core inventive features while potentially allowing further diversification via dependent claims.
  • The patent landscape indicates an active field, with overlaps possible, necessitating ongoing freedom-to-operate analyses.
  • Protection in Norway is part of a broader international patent strategy, with potential extensions into Europe, US, and globally.
  • Commercial success hinges on patent enforceability and effective positioning against competitors in the same therapeutic domain.

FAQs

1. What is the main therapeutic area covered by Norwegian Patent NO341322?
Without access to the specific claims, the exact indication cannot be confirmed. Typically, patents like NO341322 target areas such as neurology, oncology, or infectious diseases, depending on the applicant’s research focus.

2. How strong is the patent protection offered by NO341322?
The strength depends on the novelty and inventive step supported by the claims. Broad, well-defined claims covering a core compound and its uses tend to provide solid protection, but susceptibility to invalidation exists if prior art is strong.

3. Can similar patents challenge the validity of NO341322?
Yes. Related patents or publications that disclose similar compounds or methods may be used to challenge validity through prior art submissions, especially if claims are overly broad.

4. How does this Norwegian patent influence global patent rights?
While the patent is valid in Norway, national rights do not automatically extend internationally. A patent family strategy involving filings in other jurisdictions is necessary for broader protection.

5. What is the typical lifespan of a pharmaceutical patent like NO341322?
In Norway, patent protection generally lasts 20 years from the filing date, subject to maintenance fees. The commercial exclusivity depends on the patent's validity and market conditions.


References

[1] Norwegian Patent Office. Patent NO341322; filed [Insert date].
[2] European Patent Office. Patent classification details, CPC codes related to NO341322.
[3] Literature on patent strategies in pharmaceuticals, including PCT filings and patent landscape analysis methodologies.
[4] General patent law principles in Norway and European patent law.

Note: Precise claim language, patent family information, and references to the patent document are essential for a more nuanced legal and technical analysis.

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