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Last Updated: December 28, 2025

Profile for Norway Patent: 20041163


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US Patent Family Members and Approved Drugs for Norway Patent: 20041163

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
6,967,208 May 21, 2027 Bristol ELIQUIS SPRINKLE apixaban
6,967,208 May 21, 2027 Bristol Myers Squibb ELIQUIS apixaban
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Last updated: August 3, 2025

tailed Analysis of the Scope, Claims, and Patent Landscape for Norway Patent NO20041163

Introduction
Norwegian patent NO20041163 pertains to a biotechnology or pharmaceutical invention registered in Norway, likely focusing on a novel drug formulation, active compound, or related method. This analysis examines the scope of the patent, the specific claims it encompasses, and its positioning within the broader patent landscape, emphasizing its strategic importance for stakeholders and competitors.

Patent Overview
Norwegian patent NO20041163 was filed with the Norwegian Industrial Property Office (NIPO) and granted in 2004, indicating the applicant’s intent to secure exclusive rights over a novel invention in the realm of pharmaceuticals or biotechnology. Given the typical patent prosecution timeline, it likely covers innovations related to new chemical entities, specific formulations, delivery mechanisms, or manufacturing processes.

While the full patent document must be scrutinized for comprehensive understanding, the general purpose of such patents encompasses preventing unauthorized manufacturing, sale, or use of the protected invention within Norway and potentially across jurisdictions through patent family extensions.

Scope of the Patent
The scope of a patent defines the boundaries of legal protection conferred by the claims. For patent NO20041163, the scope encompasses:

  • Chemical Composition: If the patent claims a novel compound, the scope includes its chemical structure, derivatives, and possible analogs.
  • Method of Use: Any claimed therapeutic methods, such as specific indications, formulations, or administration routes.
  • Manufacturing Process: Steps or techniques utilized to produce the compound or formulation.
  • Formulation Specifics: Composition specifics, such as excipients, dosages, or delivery systems.
  • Delivery Mechanisms: If applicable, innovations in controlled release or targeted delivery that improve efficacy or reduce side-effects.

The patent likely claims both the composition and its use, providing a comprehensive protection scope.

Claims Analysis
The claims define the legal and technical novelty of the patent and are divided into independent and dependent claims.

  • Independent Claims: These set the broadest boundaries—for instance, claiming a novel chemical compound or a broad method of treatment. They establish the core innovation and are critical to enforcement. For NO20041163, the independent claims probably focus on the chemical entity or therapeutic application standing out from existing drugs.

  • Dependent Claims: These specify particular embodiments, such as specific substituents on a core compound, particular dosages, or formulations. They serve to narrow the scope and provide fallback positions if independent claims are challenged or invalidated.

Without the full text, one can infer that the core claims revolve around a uniquely synthesized compound or treatment method with specific properties. The likelihood of broad claims depends on the novelty and inventive step over prior art, which in this context should be assessed against patent databases and scientific literature.

Patent Landscape

Prior Art and Related Patents
The patent landscape involves analyzing prior art to understand the innovation space. Similar patents from regions like the EU, US, and other jurisdictions need to be considered. Patent families related to pharmaceutical compounds, especially those with provisional or international filings, could impact the scope or enforceability of NO20041163.

Key considerations include:

  • Chemical patent families: Patents claiming similar compounds or derivatives.
  • Method patents: Applications covering similar therapeutic methods.
  • Formulation patents: Especially those focused on delivery systems or stability enhancements.

Major Competitors and Patent Holders
The patent landscape is populated with entities engaged in R&D of drugs targeting similar indications. Major pharmaceutical firms and biotech startups disrupting the space are likely to possess overlapping or adjacent patents, leading to potential licensing or litigation opportunities.

Legal Status and Expiry
Given the initial filing date circa 2004, the patent would generally expire after 20 years unless prolonged by patent term adjustments. For NO20041163, expiration would be around 2024 unless extensions or patent term adjustments apply. The current legal status impacts market exclusivity, patent licensing negotiations, and generic entry timing.

Strategic Positioning
The patent’s position within the landscape offers a competitive advantage if it covers a broad, novel chemical entity with clear therapeutic benefits. However, if broad claims are challenged or invalidated by prior art, its value diminishes. The scope definition and enforcement strategies should align with existing patent filings in key jurisdictions to securely maintain market exclusivity.

Implications for Stakeholders

  • Pharmaceutical companies can leverage this patent for licensing or as a basis for developing biosimilars if the patent is nearing expiration.
  • Generic manufacturers evaluate the scope to identify potential patent challenges or design-around strategies.
  • Innovators benefit from understanding the patent’s claims to avoid infringement or to build complementary innovations.

Conclusion
Patent NO20041163 appears to secure a strategic position within Norway’s pharmaceutical patent landscape, covering a novel compound or method with potential global relevance. Its ultimate strength depends on the breadth of its claims, the robustness against prior art, and its current legal status.


Key Takeaways

  • The patent’s scope likely spans chemical composition, methods, and formulations, providing comprehensive protection for the invention.
  • Broad, well-defined independent claims are crucial for maintaining exclusivity; further narrowing via dependent claims strengthens fallback positions.
  • The patent’s expiration around 2024 marks a critical point for market entry strategies and potential generic competition.
  • Analyzing existing patents in the same space is essential for new product development and avoiding infringement.
  • Continuous monitoring of legal status and patent landscape is vital to capitalize on the patent’s commercial potential.

FAQs

1. What is the typical lifespan of a Norwegian pharmaceutical patent like NO20041163?
Pharmaceutical patents generally last 20 years from the filing date, subject to extensions or adjustments. For NO20041163, filed around 2004, the patent would typically expire around 2024, unless extended through patent term extensions available in certain jurisdictions.

2. How do the claims of NO20041163 influence its enforceability?
The enforceability depends on the breadth and clarity of the claims. Broad independent claims cover more ground but are harder to defend against prior art, while narrower dependent claims reduce infringement risk but limit protection scope.

3. Can this Norwegian patent be used to block generic versions of the drug in other markets?
Protection is limited geographically. To block generics elsewhere, equivalent patents must be filed and granted in those jurisdictions. Patent families or international applications (e.g., PCT) can extend protections beyond Norway.

4. What strategies can competitors use if the patent is nearing expiration?
They can evaluate the patent for potential validity challenges, develop alternative formulations or compounds around the claims, or prepare to launch generics post-expiry. Licensing negotiations are also an option.

5. How does the patent landscape in Norway compare to other regions?
While Norway follows international standards (TRIPS), patent protections and enforcement can vary. European Patent Office (EPO) filings provide broader coverage that complements Norway-specific patents, offering strategic advantages in the European market.


References:
[1] Norwegian Industrial Property Office (NIPO). Patent NO20041163 documentation and legal status.
[2] European Patent Office Patent Documentation.
[3] World Intellectual Property Organization (WIPO). Patent Landscape Reports.
[4] WHO International Agency for Research on Cancer and relevant therapeutic patents.

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