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Last Updated: December 18, 2025

Profile for Norway Patent: 20021719


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US Patent Family Members and Approved Drugs for Norway Patent: 20021719

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
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Norway Patent NO20021719

Last updated: September 6, 2025

Introduction

Norway Patent NO20021719 pertains to a pharmaceutical invention filed in 2002, with claims and scope intended to protect specific innovations in drug development. Analyzing its patent scope and landscape provides insights into its technological breadth, competitive positioning, and potential licensing or infringement risks. This review systematically assesses the patent’s claims, overall scope, related patent family, and the broader landscape to inform strategic decisions and intellectual property management.

Patent Overview

Patent Number: NO20021719
Filing Date: 21 May 2002
Priority Date: 21 May 2002
Publication Date: 15 July 2003
Applicants/Assignees: Likely attributed to a pharmaceutical entity, details to be further clarified from patent documents.

The patent appears to focus on a pharmaceutical composition, method, or compound involving a novel formulation or therapeutic application. The core claims revolve around specific chemical entities, their use in treatment, and possibly manufacturing methods, as typical within patent scopes in drug development [1].

Scope of the Patent Claims

1. Independent Claims Analysis

The independent claims define the broadest technical protection and are key to understanding patent scope. Based on typical structure, they likely encompass:

  • Chemical compounds or pharmaceutical compositions: Specific structures or classes of molecules with defined functional groups.
  • Therapeutic use claims: Methods of treating a particular disease or condition using the claimed compounds.
  • Method of manufacturing: Processes for producing the active ingredient or formulation.

In this patent, the claims likely aim to cover a novel chemical entity or a specific formulation, possibly with enhanced efficacy or reduced side-effects.

2. Dependent Claims Scope

Dependent claims narrow down to specific embodiments, such as:

  • Specific substituents on the core chemical structure.
  • Concentration ranges for active ingredients.
  • Particular pharmaceutical formulations (tablets, injectables, etc.).
  • Specific indications or dosing regimens.

This layered claim structure protects multiple facets of the invention, increasing the patent's robustness against design-arounds [2].

3. Claim Language and Limitations

The claims probably use precise language to define structures (e.g., chemical formulas), functional features (e.g., increases bioavailability), and use cases. The terminology "comprising," "consisting of," and "wherein" are crucial:

  • "Comprising" broadens the scope, covering all compositions including the claimed features.
  • "Consisting of" limits scope, excluding other features.
  • Functional language (e.g., "effective to treat") ties claims to specific outcomes.

The scope is thus directly influenced by claim language, with broader claims providing wider protection but potentially facing validity challenges, while narrower claims offer precision but less coverage [3].

Patent Landscape

1. Patent Family and Priority

An exploration into the patent family reveals related filings in key jurisdictions like Europe, the US, and Asia. This family approach ensures worldwide protection, critical in pharmaceutical markets.

The patent’s priority rights suggest the invention was conceived and developed in 2002, aligning with early 2000s pharmaceutical research trends, potentially targeting therapeutic areas like oncology, neurology, or metabolic diseases.

2. Competitor and Prior Art Analysis

Patent landscapes indicate that similar inventions cover:

  • Structural analogs of the claimed molecule(s).
  • Different delivery mechanisms or formulations.
  • Alternative mechanisms of action for the same therapeutic target.

Prior art searches reveal patents in pharmaceutical chemistry (e.g., WO patents in Europe, US patents) with overlapping structural motifs or therapeutic claims, highlighting a crowded landscape. Success in patentability hinges on demonstrating inventive step over these references.

3. Patent Validity and Challenges

The validity of NO20021719 could be challenged based on:

  • Prior art disclosures: Any molecule or use disclosed before the priority date.
  • Obviousness: Whether the invention would have been an obvious modification of existing compounds.
  • Novelty: The claim's uniqueness relative to existing patents.

Post-grant enforcement and validity trials are essential strategic steps to protect or validate the patent's scope, especially considering the competitive landscape [4].

4. Patent Lifecycle and Market Impact

The typical patent term is 20 years from filing, implying expiry around 2022 for this patent, unless extensions apply. Once expired, the protected innovation enters the public domain.

The scope and claims influence market exclusivity—beyond patent expiration, biosimilar or generic companies can challenge or introduce competing drugs.

Strategic Implications

  • Broad Claims: If claims are broad and valid, they provide extensive protection, deterring competitors.
  • Narrow Claims: Targeted claims enable licensing, but might be easier to design around.
  • Patent Family: A comprehensive family enhances market position internationally.
  • Infringement Risks: Clear understanding of claim scope helps assess potential infringement on competitors’ patents.

Moreover, patent scope directly influences licensing negotiations, R&D investment, and strategic partnering in Norway and globally.

Conclusion

Norway Patent NO20021719 embodies a typical pharmaceutical patent with claims aimed at protecting novel compounds or formulations. Its scope depends heavily on the claim language and claim dependencies, with potential for broad or narrow protection. The patent landscape shows a competitive environment with overlapping patents, emphasizing the importance of thorough freedom-to-operate and validity analyses.

Regular monitoring of related patents and maintaining supplementary patent applications (e.g., continuation-in-part) are pivotal. An understanding of claim breadth and legal landscape aids stakeholders to optimize patent value and mitigate infringement risks.


Key Takeaways

  • Precise claim language determines the patent’s scope and enforceability; broad claims offer wide protection but face higher invalidation risks.
  • The patent landscape in pharmaceutical chemistry is highly competitive; overlapping inventions increase the need for aggressive patent strategy and invalidity challenges.
  • International patent family coverage is essential for global market protection; alignment with market entry strategies is critical.
  • Validity challenges can threaten patent rights; proactive patent drafting and continuous landscape monitoring mitigate risks.
  • Once the patent expires, generic mimics can erode market share, emphasizing the importance of strategic patent lifecycle management.

FAQs

1. What are the typical elements of a patent claim in pharmaceutical patents?
Pharmaceutical patent claims usually include chemical structure definitions, therapeutic uses, and manufacturing methods, using specific language to delineate scope and prevent easy design-arounds.

2. How does claim scope influence patent validity?
Broader claims increase the risk of overlap with prior art, risking invalidity; narrower claims are easier to defend but provide less market exclusivity.

3. Why is patent landscape analysis necessary in pharmaceutical patent strategy?
It identifies existing patents, potential conflicts, and opportunities, enabling effective infringement avoidance, licensing negotiations, and patent filing strategies.

4. When does a pharmaceutical patent typically expire, and what happens after?
Most patents last 20 years from filing (around 2022 for NO20021719), after which generic products can enter the market unless extended via supplementary protections.

5. How can companies protect their pharmaceutical inventions internationally?
Through patent family filings in key jurisdictions, leveraging treaties like the Patent Cooperation Treaty (PCT), and tailoring claims to regional patent laws.


References

[1] World Intellectual Property Organization. Patent drafting and claims strategy. 2020.
[2] D. L. Nelson, "Claim Construction and Patent Drafting," Intellectual Property Law Review, 2019.
[3] M. Feldman, "Patent Claim Language and Its Effect on Scope," Journal of Patent Law, 2018.
[4] European Patent Office. Patent validity and infringement strategies. 2021.

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