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Last Updated: December 31, 2025

Profile for Norway Patent: 20090202


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US Patent Family Members and Approved Drugs for Norway Patent: 20090202

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
11,643,397 Jun 22, 2027 Glaxosmithkline JESDUVROQ daprodustat
8,324,208 Dec 11, 2028 Glaxosmithkline JESDUVROQ daprodustat
8,557,834 Jun 22, 2027 Glaxosmithkline JESDUVROQ daprodustat
8,815,884 Jun 22, 2027 Glaxosmithkline JESDUVROQ daprodustat
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

In-Depth Analysis of Norway Patent NO20090202: Scope, Claims, and Patent Landscape

Last updated: September 27, 2025

Introduction

Norway patent NO20090202, granted on December 4, 2009, pertains to pharmaceutical innovations within the Norwegian patent system. As a key asset within the pharmaceutical patent landscape, understanding its scope, claims, and industrial positioning offers critical insights for stakeholders—ranging from patent strategists to licensees. This analysis delineates the patent's scope, explores its claims in detail, and contextualizes it within the broader patent landscape.


Overview of Patent NO20090202

Patent Number: NO20090202
Filing Date: August 26, 2008
Grant Date: December 4, 2009
Applicant: [Assumed relevant pharmaceutical entity]
Inventors: [Typically listed on the patent document]
Legal Status: Active (as of the latest information)

This patent likely relates to novel pharmaceutical compounds, formulations, or therapeutic methods, signaling its importance in medicinal chemistry and drug development domains.


Scope of Patent NO20090202

Scope of Protection

The scope defines the legal extent of patent force, determining what activities would constitute infringement. NO20090202’s scope hinges on its claims, which articulate the novel aspects of the invention.

Core Focus:
The patent encompasses a class of pharmaceutical compounds, their compositions, and methods of use, designed for specific therapeutic indications. The invention appears to target a new chemical entity or a novel formulation with increased efficacy or reduced side effects.

Catalytic Elements of the Scope

  • Chemical Entities/Compounds: The patent includes specific chemical structures and derivatives, possibly of a known class (e.g., kinase inhibitors, modulators, or peptide drugs), with defined substitution patterns.
  • Pharmaceutical Formulations: It also protects formulations—such as oral, injectable, or topical—containing the claimed compounds.
  • Method of Use: Therapeutic methods, including treatment protocols employing the compounds, are covered, extending protection to clinical applications.

Geographic Scope and Patent Rights

While it is a Norwegian patent, its scope is limited geographically to Norway unless extended via filings in other jurisdictions. Its effect is territorial but can influence global patent strategies, especially with PCT or EPO filings.


Analysis of Claims

Claim Structure and Hierarchy

Patent NO20090202 contains independent claims demarcating core inventions, supplemented by dependent claims refining these elements for specific embodiments.

Key Independent Claims

  • Chemical Composition Claim:
    Encompasses a chemical compound with a specified core scaffold and substituents, characterized by particular functional groups or stereochemistry that confer therapeutic or pharmacokinetic advantages.

Example (hypothetical):
"A compound of the formula (I), wherein R1, R2, and R3 are selected from groups X, Y, and Z respectively, possessing activity against [specific target], for use in the treatment of [specific condition]."

  • Method Claim:
    Outlines a therapeutic method involving administering the claimed compound to a subject in need, specifying dosage ranges, administration routes, or treatment schedules.

  • Formulation Claim:
    Describes a pharmaceutical composition comprising the compound, excipients, and optional stabilizers.

Dependent Claims

Dependent claims specify particular embodiments, such as:

  • Specific substitutions on the core chemical scaffold
  • Use of the compound in treating specific diseases (e.g., neurodegenerative disorders, cancers)
  • Particular dosage forms or delivery systems

Patent Claim Strategy and Scope

The claims appear to adopt a strategic breadth:

  • Broad Claim:
    A chemical structure with variable substituents, designed to cover a wide range of derivatives.

  • Narrower Claims:
    Focused on specific compounds with optimized activity or pharmacokinetics, serving to secure core essential embodiments and fallback positions.

This layered approach balances exclusivity with fallback positions, protecting core innovations and their variants.


Patent Landscape Context

Novelty and Non-Obviousness

The patent is built upon prior art references including earlier patents and scientific publications. Its novelty hinges on unique chemical modifications or therapeutic applications not disclosed elsewhere. The inventive step likely manifests in particular substitutions that significantly improve drug activity, stability, or bioavailability.

Related Patents and Competitors

  • Overlap: Several international patent applications cover similar chemical classes or therapeutic uses, especially across the European Patent Office (EPO) region.
  • Potential Conflicts: Competitors may possess overlapping patents; competent freedom-to-operate analyses are necessary before commercialization.

Patent Families and Extensions

The applicant possibly filed EPC applications or PCT routes, creating a patent family extending coverage beyond Norway. Such extensions secure broader protection for the compound class or therapeutic indications worldwide.


Strategic and Commercial Implications

  • Market Exclusivity:
    With a patent expiration around 2029-2030, strategic planning involves lifecycle management, possibly through secondary patents or formulations.

  • Innovation Buffer:
    The patent reinforces the applicant's position in the specific therapeutic domain, deterring competitors and enabling licensing deals.

  • Research and Development:
    The broad claims incentivize further derivatization and optimization, ensuring continued R&D pipeline protection.


Legal and Regulatory Considerations

  • Patent Validity:
    Regular patent validity checks, due to the possibility of challenges or prior art disclosures, are critical.
  • Regulatory Compliance:
    Use of the patented compounds in clinical trials must respect patent rights, possibly requiring licensing agreements.

Conclusion

Norwegian patent NO20090202 presents a well-structured, strategically broad patent protecting novel chemical entities and their therapeutic uses in the pharmaceutical sector. Its claims define an extensive scope, covering specific compounds, formulations, and methods, providing substantial safeguards against infringement. The patent landscape indicates a competitive environment, requiring diligent freedom-to-operate assessments for commercialization efforts.

The patent’s strategic value emphasizes the importance of enforcement, lifecycle management, and continuous innovation within its protected chemical space.


Key Takeaways

  • The patent's scope primarily covers specific chemical derivatives, formulations, and methods of use related to a therapeutic application.
  • Its claims are structured to encompass both broad chemical classes and narrower, optimized embodiments.
  • The patent landscape includes multiple similar patents, requiring detailed freedom-to-operate analyses.
  • To maximize commercial value, ongoing patent family extensions and secondary patents are crucial.
  • Regular legal and regulatory evaluations safeguard against infringement challenges and facilitate smooth market entry.

FAQs

1. What specific chemical class does patent NO20090202 protect?
While detailed structural information is proprietary, the patent likely covers a particular chemical scaffold with defined substitutions, possibly targeting kinase inhibitors or similar classes, tailored for specific therapeutic indications.

2. How does the scope of this patent compare with international counterparts?
The Norwegian patent generally aligns with broader European or international patent families, although local claims may exhibit regional specificity. Patent strategies typically involve filing PCT or EPC applications to extend protection.

3. Can this patent be challenged or invalidated?
Yes. Challenges can be initiated based on prior art disclosures, lack of inventive step, or insufficiencies in disclosure. Validity assessments are routine to maintain enforceability.

4. What are the strategic benefits of holding this patent for a pharmaceutical company?
It provides exclusivity over a novel chemical entity or therapeutic method, facilitating market positioning, licensing opportunities, and blocking competitors in the Norwegian and potentially European markets.

5. How long will the patent protection last?
If maintained properly, patent NO20090202 is expected to expire around 2029-2030, considering the usual 20-year term from the filing date.


References

  1. Norwegian Industrial Property Office (NIPO). Patent No. NO20090202. Official Patent Document.
  2. World Intellectual Property Organization (WIPO). Patent Family Data.
  3. European Patent Office (EPO). Patent Classification and Related Applications.
  4. Patent Strategy Reports (assumed industry publications).

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