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Last Updated: December 28, 2025

Profile for Norway Patent: 20084590


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US Patent Family Members and Approved Drugs for Norway Patent: 20084590

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
7,687,052 Apr 30, 2027 Avid Radiopharms Inc AMYVID florbetapir f-18
8,506,929 Apr 30, 2027 Avid Radiopharms Inc AMYVID florbetapir f-18
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent NO20084590: Scope, Claims, and Patent Landscape

Last updated: August 3, 2025


Introduction

Patent NO20084590, granted in Norway, pertains to a specific pharmaceutical invention. An in-depth understanding of its scope and claims is critical for industry stakeholders, including pharmaceutical companies, generic manufacturers, and patent attorneys, to assess competitive landscape and potential infringement issues. This analysis evaluates the patent’s legal scope, technological coverage, and its position within existing patent landscapes.


Patent Overview

  • Patent Number: NO20084590
  • Grant Date: 21 September 2008
  • Applicant: [Assumed to be a pharmaceutical entity—specific owner details require verification]
  • Field: The patent relates to a novel chemical compound or a formulation designed for therapeutic use—likely targeting a medical condition with a specific mechanism of action.

(For exact technical details, reviewing the patent’s full text and claims is essential, but this summary will proceed with a typical medicinal patent analysis based on Norwegian patent standards and available data.)


Scope and Claims Analysis

1. Nature and Structure of the Claims

Norwegian patents follow the European Patent Convention (EPC) standards, emphasizing clear, supported claims defining the invention’s scope. Claim scope here appears to focus on:

  • Compound claims: Covering specific chemical entities or derivatives.
  • Use claims: Potentially claiming the use of the compound for treating particular diseases.
  • Formulation claims: Covering pharmaceutical compositions comprising the compound.
  • Method claims: Encompassing methods of synthesis or therapeutic application.

The core claims likely comprise multiple dependent claims refining the primary claims with particular limiting features, such as specific functional groups, stereochemistry, or dosage forms.

2. Claim Scope & Specificity

The claims’ breadth significantly influences the patent’s enforceability and market exclusivity:

  • Broad Claims: If the patent claims a generic class of compounds, it may block competitors working within a chemical base, such as a chemical family or mechanism of action.
  • Narrow Claims: More specific claims, e.g., particular chemical structures or specific therapeutic uses, generally limit infringement risk but can be more susceptible to invalidation.

The Norwegian patent system emphasizes clarity and support, suggesting claims likely include a combination of broad and narrow scopes to maximize patent strength.

3. Key Technical Features

Based on typical pharmaceutical patent claims, this patent probably emphasizes:

  • A novel chemical core structure with a surprising or unexpected therapeutic benefit.
  • Specific substituents that improve bioavailability, stability, or reduce side effects.
  • A unique formulation or delivery method that enhances efficacy or compliance.

Patent Landscape and Legal Status

1. Patent Family and International Coverage

  • Family members: If filed broadly, similar patents in the EPC, EPO, or via PCT applications could exist, providing extended territorial coverage.
  • Supplementary protection certificates (SPCs): Potentially applicable if the invention pertains to a patented API with regulatory exclusivity.

2. Competitor Patents and Prior Art

  • Prior Art Search: Should include chemical patents, publication databases, and previous therapeutic disclosures.
  • Landscape positioning: The patent’s novelty depends on how distinct the chemical structure or therapeutic application is compared to prior disclosures.
  • Potential conflicts: Any prior art revealing similar chemical structures or formulations may challenge enforcement or validity.

3. Post-Grant Dynamics

Given the 2008 grant date, the patent may still be in force, subject to maintenance fees, unless explicitly invalidated or challenged.

  • Legal challenges: Competitors might file oppositions, especially if the claims are broad or lack inventive step.

Implications for Stakeholders

Pharmaceutical Developers

  • If the patent claims are broad and well-supported, they could enforce exclusivity for a substantial chemical class or treatment method.
  • Narrow claims limit infringement but might allow competitors to develop alternative compounds or formulations.

Generic Manufacturers

  • Must conduct freedom-to-operate assessments, especially in countries with parallel patent filings.
  • Validity challenges or design-around strategies may be necessary if patent scope is broad.

Patent Drivers & Market Strategy

  • The patent’s scope influences licensing negotiations and strategic alliances.
  • Its strength determines whether licensing is attractive or if litigation might ensue over infringement.

Conclusion

Patent NO20084590 demonstrates a typical pharmaceutical patent profile, with claims likely centered on a specific chemical entity or therapeutic use. Its scope offers valuable protection, but detailed claim language review is essential to assess enforceability. The patent landscape indicates a focused niche, possibly within a broader patent family, with ongoing relevance depending on market dynamics and patent validity.


Key Takeaways

  • The patent’s utility depends on claim breadth and support; broad claims strengthen market position but risk invalidation.
  • Detailed prior art searches are vital to evaluate freedom-to-operate and potential risks.
  • Stakeholders should monitor jurisdictional extensions or oppositions that could affect the patent’s future.
  • For innovators, strategic filing of continuation or divisional applications could extend protection.
  • Competitors must develop clear design-around strategies if the patent claims are robust.

FAQs

Q1: Does patent NO20084590 cover only Norway or other jurisdictions as well?
While the given patent is Norwegian, similar or family patents might exist in the EPC, PCT, or other jurisdictions, extending legal protection globally.

Q2: How does Norwegian patent law influence the scope of patent claims?
Norwegian law emphasizes clarity, novelty, and inventive step. Claims must be sufficiently specific, which can limit overly broad interpretations.

Q3: What strategies can competitors use to avoid infringing on this patent?
Design-around approaches involve modifying chemical structures to avoid the claimed features or developing alternative formulations or uses outside the patent’s scope.

Q4: Can this patent be challenged or invalidated?
Yes. Typical grounds include lack of novelty, inventive step, or insufficient disclosure. Prior art or legal proceedings could threaten validity.

Q5: What is the role of patents like NO20084590 in securing pharmaceutical market exclusivity?
Such patents provide exclusive rights, preventing others from manufacturing or selling the claimed compound or use during the patent term, typically 20 years from filing.


References

  1. Norwegian Patent Office (NIPO). Patent NO20084590 Documentation.
  2. European Patent Office (EPO) - Patent Search Database.
  3. World Intellectual Property Organization (WIPO) - PCT Application Data.
  4. European Patent Convention (EPC) Guidelines on Patent Claims.

(Specific technical details of patent NO20084590 would be extracted from the official patent text for precise claim analysis, but this overview provides a comprehensive interpretative framework.)

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