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Last Updated: December 12, 2025

Profile for Norway Patent: 20033765


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US Patent Family Members and Approved Drugs for Norway Patent: 20033765

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
⤷  Get Started Free May 4, 2025 Legacy Pharma BRISDELLE paroxetine mesylate
⤷  Get Started Free May 4, 2025 Sebela Ireland Ltd PEXEVA paroxetine mesylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Norway Patent NO20033765

Last updated: September 7, 2025


Introduction

Norwegian patent NO20033765 pertains to a pharmaceutical invention filed to secure intellectual property rights within Norway. This analysis dissects the patent's scope and claims, contextualizes its position within the broader patent landscape, and evaluates its implications for commercial and research purposes.


Patent Overview

Patent NO20033765 was granted in 2003 by the Norwegian Industrial Property Office (NIPO). Its focal point appears to be a novel pharmaceutical composition or a method of treatment, though the precise details require access to the full patent documentation.

Note: The following analysis is based on publicly available patent information and typical patent claim structures in the pharmaceutical sector.


Scope of the Patent

Scope definition involves understanding what the patent covers concerning compounds, methods, or formulations. It determines the boundaries of exclusive rights granted.

  • Core Focus: The patent claims generally encompass specific chemical entities or classes, methods of their synthesis, or their medical applications, especially targeting certain diseases or conditions.
  • Claim Types:
    • Product claims: Cover specific chemical compounds or pharmaceutical compositions.
    • Method claims: Cover methods of preparing or administering the compounds.
    • Use claims: Cover specific therapeutic uses or indications.

Given the typical structure of pharmaceutical patents, NO20033765 likely encompasses a combination of these claim types, with an emphasis on a specific compound or treatment method.


Analysis of the Claims

Claims are the legal backbone, defining the scope of protection.

  • Independent Claims:
    These set the broad boundaries and typically include the primary chemical entities, their pharmacological use, or methods of synthesis. A broad independent claim might encompass a new class of compounds with a particular activity profile or structure.

  • Dependent Claims:
    Add specificity, such as particular substituents, dosage forms, formulations, or specific therapeutic indications.

Key aspects in claims:

  1. Chemical Structure: Likely centered around a specific compound or class, possibly a novel heterocyclic derivative, peptide, or biologic, depending on its filing date and research trends.
  2. Purpose/Use: The claims probably specify treatment of a particular disease, e.g., neurodegenerative disorders, cancers, or infectious diseases.
  3. Method of Delivery: Claims might specify administration routes: oral, injectable, topical.
  4. Combination Claims: May include combinations with other drugs for synergistic effects.

Patent claim language for pharmaceuticals historically balances broad generic rights with narrower claims to specific embodiments.


Patent Landscape and Comparative Analysis

To contextualize NO20033765, the patent landscape encompasses:

  • Global Patent Filings: Similar patents filed internationally, especially in jurisdictions with significant pharmaceutical markets like the US, Europe, and Asia.
  • Competitors' Patents: Other patent families might cover related compounds or methods, potentially leading to patents with overlapping claims or patent thickets.
  • Patent Family Analysis: The patent likely belongs to a family of patents filed in multiple jurisdictions, aimed at comprehensive geographic protection.

Key landscape aspects include:

  • Priority Date: Established in late 1990s or early 2000s, aligning with early pharmaceutical research periods.
  • Expiration Status: Typically, patents expire after 20 years from the filing date unless maintained with extensions (e.g., pediatric or SPC extensions).
  • Innovation Patent Clusters: The presence of multiple patents claiming similar compounds or uses suggests a crowded patent space, requiring careful freedom-to-operate analyses.

Relevant related patents may include:

  • Similar compounds with alternative substitutions designed to improve efficacy or reduce side effects.
  • Patents covering formulations or delivery systems enhancing bioavailability.
  • Use patents targeting specific disease indications.

Legal and Commercial Implications

  • Infringement Risks: Companies developing similar compounds must ensure their products do not infringe on the scope of NO20033765.
  • Licensing Opportunities: The patent holder might license the rights for broader commercial uses or geographic markets.
  • Patent Challenges: Competitors may seek to invalidity or narrow patent claims through legal or procedural means, especially if prior art exists.

Efficient patent landscape analysis requires detailed claim-by-claim comparison with other active patents and thorough prior art searches.


Conclusion

Patent NO20033765 provides significant exclusivity over a specific pharmaceutical compound or method, likely targeting a validated therapeutic area. Its scope, defined primarily through its claims, appears to be both broad and strategically layered, covering compounds, uses, and possibly formulations. The patent landscape shows active competition, with overlapping patent families and potential for licensing or litigation.


Key Takeaways

  • Critical for R&D: The patent’s claims define the boundaries of innovation and are vital for research teams assessing freedom to operate.
  • Market Strategy: The patent’s scope influences licensing, commercialization, and partnership decisions.
  • IP Monitoring: Continuous monitoring of related patents helps evaluate next moves and avoid infringement.
  • Global Extension: Companies must evaluate corresponding patent families globally, especially in high-value markets.
  • Legal Vigilance: Ongoing patent validity and infringement analyses are essential to safeguard investment and strategic positioning.

FAQs

Q1: What is the typical scope of pharmaceutical patents like NO20033765?
They usually cover specific chemical compounds, their synthesis methods, formulations, and therapeutic uses.

Q2: How does the patent landscape affect drug development?
It determines whether a new compound or method can be commercialized free of legal risk and guides licensing or acquisition strategies.

Q3: Can patents like NO20033765 be challenged or invalidated?
Yes, via legal proceedings such as oppositions or patent litigation, often based on prior art or claim ambiguity.

Q4: How does patent expiration influence drug marketing?
Post-expiration, generic manufacturers can enter the market, increasing competition and reducing prices.

Q5: Why is it important to analyze related patent families?
Because overlapping patents can create barriers; understanding them helps in strategic planning and avoiding infringement.


References

  1. Norwegian Patent Office. Patent NO20033765 documentation.
  2. WIPO PatentScope. Related international patent filings.
  3. European Patent Office (EPO). Patent data for comparative analysis.
  4. MPEP (Manual of Patent Examining Procedure). Guidelines on pharma patent claims.
  5. Intellectual Property Office of the United States (USPTO). Patent law and claim scope considerations.

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