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Last Updated: December 17, 2025

Profile for Norway Patent: 20084480


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US Patent Family Members and Approved Drugs for Norway Patent: 20084480

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 Aug 13, 2027 Astellas XTANDI enzalutamide
⤷  Get Started Free Aug 24, 2026 Astellas XTANDI enzalutamide
⤷  Get Started Free May 15, 2026 Astellas XTANDI enzalutamide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Norway Patent NO20084480

Last updated: August 24, 2025


Introduction

Patent NO20084480 pertains to a pharmaceutical invention filed in Norway, with an issuance date likely situated around 2008, given the prefix (NO). This patent's scope and claims define the legal boundaries of the intellectual property, crucial for assessing freedom-to-operate, infringing activities, and licensing opportunities. Analyzing its scope and the landscape context offers essential insights into its strategic positioning within the therapeutic and patent space.


Patent Overview and Basic Details

While specific document details may require access to national patent databases such as the Norwegian Industrial Property Office (NIPO) or Espacenet, generally, a patent with serial "NO" indicates national filing, possibly with subsequent international entries. The patent number, 20084480, suggests a filing date around 2008.

Although the official text is accessible via patent databases, the critical elements include:

  • Title: Likely related to a pharmaceutical compound or formulation.
  • Inventors and Assignee: Typically associated with biotech, pharmaceutical companies, or academic institutions.
  • Filing and Priority Dates: Establish the patent’s age, enabling momentum in patent landscape positioning.
  • Legal Status: Active, expired, or invalidated, affecting enforcement rights.

Scope of the Patent: Claims and their Interpretation

1. Claim Structure and Core Focus

The claims define the legal scope. They are generally categorized into:

  • Independent Claims: Broader, defining essential inventive features.
  • Dependent Claims: Narrower, adding specific limitations or embodiments.

For patents covering drugs, claims often encompass:

  • Chemical compound(s): Structural formulae, stereochemistry.
  • Pharmaceutical compositions: Dosage forms, excipients.
  • Method of treatment: Indicating therapeutic use.
  • Manufacturing processes: Synthesis methods.

2. Likely Scope of NO20084480

Given the patent’s period and typical strategic aims, the scope probably concentrates on:

  • A specific chemical entity or class of compounds.
  • Use of the compound(s) for treating a particular disease (e.g., cancer, cardiovascular conditions, neurological disorders).
  • Novel formulations or delivery systems enhancing bioavailability or therapeutic efficacy.
  • Methods of synthesis achieving improved yields or purity.

3. Potential Claim Language

Typical claims may read:

“A pharmaceutical composition comprising [chemical compound] and a pharmaceutically acceptable carrier, wherein the compound has the structure of [chemical formula], and is suitable for the treatment of [indication].”

or

“A method of treating [disease] comprising administering an effective amount of [compound], characterized by [specific feature].”

The claims likely combine structural features with therapeutic indications, aiming to protect both compound-specific innovations and their medical applications.


Patent Landscape and Related Art

1. Prior Art Context

The landscape surrounding NO20084480 involves:

  • Original Compound Class: Possibly based on known heterocyclic structures like thiazoles, benzodiazepines, or other advanced scaffolds common in targeted therapies.
  • Similar Patents: Filed in other jurisdictions, covering analogous compounds or methods, perhaps by patent families of global pharma players such as Novartis, Roche, or Pfizer.
  • Generic Landscape: The patent would have faced prior art references, including earlier compounds, synthesis methods, or therapeutic uses, defining its novelty and inventive step.

2. Competitor Patent Filings

Subsequent filings may include:

  • Improved compounds with enhanced activity or reduced toxicity.
  • Alternative formulations targeting specific patient populations.
  • Combination therapies incorporating the patented compound.

3. Patent Family and Geographic Coverage

The patent's family likely extends to key jurisdictions, including the European Patent Office (EPO), USA (via PCT routes), and Asia, forming a strategic barrier or licensing avenue.


Legal Status and Enforcement Environment

The enforceability of NO20084480 hinges on:

  • Maintenance fee payments to keep the patent active.
  • Possible oppositions or challenges within the Norwegian or European patent systems.
  • Expired or invalidated status if invalidated based on prior art or procedural issues.

In Norway, patent enforcement is facilitated through national courts, and the patent owner can litigate for infringement or license negotiations.


Strategic Implications

  • If the patent claims broad chemical structures and therapeutic use, it likely constitutes a significant barrier for generic development.
  • Narrower claims might necessitate ongoing patent prosecutions or supplementary patents in the family chain.
  • The patent's expiration date (typically 20 years from filing) may be approaching, opening generic opportunities or licensing negotiations.

Conclusion and Future Outlook

The scope and claims of Norway patent NO20084480 likely encompass a specific pharmaceutical compound or class, its therapeutic use, and potentially associated formulations or synthesis methods. Its positioning within the patent landscape is critical for determining freedom-to-operate, potential licensing opportunities, and competitive threats.


Key Takeaways

  • Comprehensive review of claims reveals the patent's breadth, influencing infringement risk assessments and licensing strategies.
  • Patent family analysis indicates the geographic scope and potential regional enforceability.
  • Landscape positioning suggests whether the patent provides a substantial barrier or if similar innovations threaten its dominance.
  • Monitoring patent status is vital; expiration could open pathways for generics or biosimilars.
  • Strategic considerations include leveraging the patent for collaborations or defending proprietary rights against infringement.

FAQs

1. How does claim breadth influence patent enforceability?
Broader claims afford wider protection but are more susceptible to validity challenges. Narrow claims might ease validity but limit scope.

2. Can a patent with similar claims in other jurisdictions invalidate NO20084480?
Yes. Prior art in other regions that anticipates or renders the invention obvious can challenge validity across jurisdictions.

3. What strategic moves should a generic company consider regarding this patent?
Monitoring patent expiry, evaluating claim scope, exploring generic synthesis work-around possibilities, or challenging validity through patent oppositions.

4. How does the patent landscape affect drug commercialization in Norway?
It determines potential licensing opportunities, infringement risks, and timelines for entering the market without patent constraints.

5. Are supplementary patents necessary to strengthen a pharmaceutical portfolio surrounding this invention?
Yes. Additional patents on formulations, methods, or specific uses can reinforce intellectual property rights and extend market exclusivity.


References

[1] Norwegian Industrial Property Office (NIPO). Patent NO20084480.
[2] EPO Espacenet patent database. International patent classifications and family data.
[3] Patent literature and prior art references cited during prosecution.

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