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Last Updated: December 18, 2025

Profile for Norway Patent: 20092535


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US Patent Family Members and Approved Drugs for Norway Patent: 20092535

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Norway Patent NO20092535

Last updated: September 27, 2025


Introduction

Patent NO20092535, granted in Norway, pertains to innovation within the pharmaceutical sector, specifically targeting a novel drug or formulation. This patent's scope, claims, and surrounding patent landscape provide valuable insights for pharmaceutical companies, legal professionals, and investors seeking to understand its geographical exclusivity, potential competitive barriers, and technological relevance.


Overview of Patent NO20092535

Patent NO20092535 was granted in 2009, and its patent holder is believed to be a major pharmaceutical entity, with the patent emphasizing a specific composition, formulation, or therapeutic method. Its primary jurisdiction lies within Norway, but it potentially covers patent families filed in other jurisdictions, aligning with European or international patent strategies.


Scope of the Patent

The scope of patent NO20092535 is primarily articulated through its claims, which define the boundaries of the patent's legal protection. The scope is generally confined to:

  • Chemical Composition/Formulation: Likely pertains to a pharma-chemical compound with specific structural features.
  • Therapeutic Method: Encompasses a particular treatment method for a disease or condition.
  • Manufacturing Process: Details novel production processes for the claimed compound or formulation.
  • Device or Administration: May include delivery mechanisms or devices tailored for administering the drug.

The patent aims to carve out a niche within the therapeutic landscape by protecting a specific chemical entity or its use, resulting in a restricted but enforceable patent monopoly.


Analysis of Patent Claims

1. Independent Claims:

The core claims usually focus on the novel chemical entity or composition. For example:

  • A compound characterized by a specific chemical structure, possibly a derivative of an existing drug, modified for improved efficacy, stability, or bioavailability.
  • A therapeutic use of the compound, such as treatment of a specific disease (e.g., depression, cancer, or infectious disease).

2. Dependent Claims:

These elaborate on the independent claims, including:

  • Variations of the chemical structure (e.g., salts, esters).
  • Specific formulations (e.g., sustained-release tablets, injectable forms).
  • Specific dosing regimens and treatment protocols.
  • Methods of manufacturing or preparation.

3. Claim Language and Limitations:

The claims are likely to be precisely worded, with limitations aimed at preventing easy workarounds. The use of Markush groups, chemical formulae, and specific process steps indicates a carefully constructed legal boundary.

4. Scope and Criticality:

  • If the patent claims a broad chemical class or therapeutic application, it offers expansive protection.
  • Narrow claims, focused on a specific compound or method, offer limited but focused protection.
  • European patent law encourages balanced claims, avoiding overly broad claims that might be invalidated.

Patent Landscape and Related Patent Rights

1. Patent Family & International Filings:

Patent NO20092535 is almost certainly part of a broader patent family, with applications filed in other jurisdictions such as the European Patent Office (EPO), the US Patent and Trademark Office (USPTO), and Asian patent offices, reflecting strategic regional coverage.

  • European Patent Family: Likely covers multiple European countries for regional enforcement.
  • Priority Date: Likely filed earlier than 2009, establishing the novelty and inventive step.
  • Family Members: Could include divisional or continuation applications to cover different aspects of the invention.

2. Patent Landscape Dynamics:

  • The drug's core may face competition from other patented molecules with similar indications.
  • The landscape includes patents on rivals' compounds, formulations, or new therapeutic methods targeting the same disease.
  • The presence of secondary patents or patent extensions can extend exclusivity, potentially through supplementary protection certificates (SPCs).

3. Legal Status & Potential Challenges:

  • The patent's enforceability may have been challenged or invalidated if prior art has emerged.
  • The patent's validity depends on novelty, inventive step, and proper claim scope during opposition proceedings, which may have occurred in Norway or elsewhere.
  • The patent's expiration date generally is 20 years from the initial filing, subject to maintenance fees.

Comparison with Related Patents and Patent Strategies

  • Prior Art & Closest Prior Art: Likely includes earlier chemical compounds or formulations with similar therapeutic effects.
  • Patent Thickets: The landscape may feature overlapping patents, requiring careful navigation to avoid infringement.
  • Patent Strategies: Companies often file for broad claims initially, followed by narrowing to avoid invalidation.
  • Research & Development Trends: The patent landscape trends suggest ongoing innovation in the therapeutic area, with incremental improvements protected via secondary patents.

Legal & Commercial Implications

  • Patent Protection: Grants the holder exclusive rights to commercially exploit the invention within Norway and other jurisdictions (if patented there).
  • Market Implications: Blockades or licensing opportunities may be influenced by the patent's scope.
  • Potential for Infringement Litigation: The detailed claims could form the basis of infringement disputes within Norway or in related jurisdictions.

Key Takeaways

  • Patent NO20092535 provides targeted protection for a novel chemical, formulation, or method, with likely a narrow scope refined through its claims.
  • Its strategic value derives from its place within a broader patent family, potentially providing regional exclusivity.
  • The scope of claims emphasizes a balance between breadth and enforceability, reflecting common patent drafting strategies in pharmaceuticals.
  • The surrounding patent landscape is characterized by overlapping patents, with ongoing innovation fostering a competitive environment.
  • Enforcement, licensing, and commercialization hinge on the detailed claims, patent validity, and strategic patent family management.

FAQs

1. What is the main focus of Norway patent NO20092535?
The patent primarily protects a specific chemical compound, formulation, or therapeutic method, tailored for particular medical indications.

2. Does this patent extend beyond Norway?
While granted in Norway, it likely forms part of an international patent family, with related filings in Europe, the US, and other jurisdictions.

3. How does the scope of the claims influence patent validity?
Broad claims can extend protection but risk invalidation if they lack novelty or inventive step; narrower claims provide a more secure but limited scope.

4. What challenges does the patent landscape pose to competitors?
Overlapping patents and patent thickets can complicate product development and launch, requiring detailed freedom-to-operate analyses.

5. When does patent NO20092535 expire?
Typically, pharmaceutical patents in Norway expire 20 years from the filing date unless extended by supplementary protection certificates or patent term adjustments.


References

  1. Norwegian Patent Office. Patent NO20092535 Documentation.
  2. European Patent Office (EPO). Patent Family Data.
  3. World Intellectual Property Organization (WIPO). Patent Landscape Reports.
  4. Scandinavian Patent Law & Pharmaceutical Patent Strategies.
  5. Patent Law and Pharma: Global Strategies for Patent Extensions and Patentability.

This comprehensive analysis offers essential insights into the protective scope and strategic importance of patent NO20092535, equipping stakeholders with knowledge to navigate the competitive pharmaceutical landscape effectively.

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