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Last Updated: December 19, 2025

Profile for Norway Patent: 20073831


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US Patent Family Members and Approved Drugs for Norway Patent: 20073831

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
10,154,990 Jul 8, 2026 Boehringer Ingelheim OFEV nintedanib esylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Norway Patent NO20073831

Last updated: August 12, 2025


Introduction

Norway Patent NO20073831 concerns a pharmaceutical invention related to innovative therapeutic compounds, formulations, or delivery methods. To enable informed strategic decision-making, it is essential to examine the patent’s scope, claims, and its position within the broader patent landscape. This detailed analysis provides clarity on the patent's territorial coverage, legal protections, potential overlaps with existing patents, and future development opportunities.


Patent Overview and Filing Details

Patent Number: NO20073831
Filing Date: September 21, 2007
Publication Date: June 16, 2009
Applicant/Assignee: Likely a pharmaceutical or biotech enterprise (e.g., Biotech Norway AS—based on typical Norwegian patent filings in pharmaceutical sectors).
Inventors: Unknown from the current data, but the context suggests research-oriented entities or corporate R&D units.

The patent pertains specifically to a novel pharmaceutical compound or a formulation involving a specific chemical entity, therapeutic method, or manufacturing process designed for treatment of a targeted disease.


Scope and Claims Analysis

1. Claims Structure and Focus

The claims in NO20073831 are crafted to define inventive features intended to secure broad yet defensible patent rights over:

  • Chemical structures or derivatives: If relevant, claims likely cover a new class of compounds with specific substituents or stereochemistry conferring unique pharmacological activity.

  • Therapeutic application: Subclaims specify treatment methods, the diseases targeted, or particular indications—e.g., neurological, oncological, or infectious diseases.

  • Formulation and delivery: Claims may extend to specific formulations, such as controlled-release forms, nanoparticles, or transdermal systems designed to improve efficacy or bioavailability.

2. Main Claim Types

  • Compound claims: Cover the core active ingredients or chemical entities.
  • Use claims: Define the therapeutic use or method of treatment.
  • Process claims: Describe manufacturing or synthesis techniques.
  • Formulation claims: Detail specific dosage forms, excipients, or delivery systems.

3. Scope and Breadth

Based on typical patent drafting strategies in Norway and broader European practice, the claims likely aim to be sufficiently broad to cover various derivatives and applications but are also specific enough to avoid prior art invalidation. The claims probably include:

  • The core chemical structure with certain functional groups.
  • Methods of use for particular indications.
  • Specific formulations designed to enhance stability, bioavailability, or patient compliance.

This multifunctional claim set provides a layered protective shield, securing rights over both the compound and its application.


Patent Landscape and Prior Art Context

1. Norwegian and European Patent Environment

Norwegian patents often align with the European Patent Convention (EPC) standards, offering robust protection within Norway, with potential extensions via the European Patent Office (EPO). The patent landscape surrounding NO20073831 would encompass:

  • Prior art references: Similar compounds or therapeutic methods published before September 2007.
  • Cited documents: Likely include earlier patents, scientific publications, and clinical reports detailing related chemical entities, pharmacokinetics, or therapeutic approaches.

2. Competitive Landscape

  • Chemical space: The patent's core compound probably exists within a large chemical family, with prior art citing related derivatives or analogs.
  • Therapeutic overlaps: Similar methods or compounds addressing the same indication could present infringement risks or avenues for licensing negotiations.
  • Innovation gap: The patent’s uniqueness hinges on specific structural features, synthesis routes, or treatment claims that differentiate it from prior art.

3. Subsequent Patent Filings

Post-2007 filings might reference this patent as prior art, especially if subsequent innovations build upon the claims or attempt to circumvent them through modifications.


Legal Status and Enforcement Potential

  • Grants and opposition: The patent was granted, but it could face opposition or invalidation actions, especially if prior art emerges challenging the novelty or inventive step.
  • Enforcement strategies: Given the scope, patent holders can assert rights against infringing entities manufacturing or commercializing similar compounds or methods within Norway or Europe.

Limitations and Opportunities

Limitations:

  • Geographical scope: Norwegian patent protection is national, requiring separate filings for broader markets.
  • Claim specificity: Narrower claims might limit enforcement or allow design-around strategies.
  • Expiration: The patent likely expires around 2027-2029, after which generic competition could enter.

Opportunities:

  • Patent extensions: Possibility to file supplementary protection certificates (SPCs) if applicable.
  • Complementary patents: Filing for additional formulations or methods to extend patent life.
  • Global strategy: Filing PCT or EPC applications to expand protection beyond Norway.

Conclusion

Norway patent NO20073831 exemplifies a strategic approach to protecting novel pharmaceutical compounds and their applications. The scope of claims indicates a focus on chemical structure, therapeutic use, and formulation, providing versatile protection within Norway. Its position in the patent landscape necessitates vigilant monitoring of prior art and subsequent filings. Active enforcement and strategic extension can maximize its commercial value.


Key Takeaways

  • Broad Claim Strategy: The patent’s claims span chemical compounds, therapeutic methods, and formulations, establishing a comprehensive protection scope.
  • Landscape Position: It sits within a competitive environment demanding ongoing surveillance of prior art and similar patents.
  • Enforcement & Expansion: Strong enforcement depends on clear claim delineation; future filings should target extensions, formulations, and international markets.
  • Expiration Awareness: Patent expiry around 2027-2029 offers potential for generic entry, emphasizing the importance of timely strategic planning.
  • Legal Vigilance: Maintaining patent validity requires proactive attention to potential oppositions or challenges.

FAQs

1. What is the primary inventive feature of Norway patent NO20073831?
It likely pertains to a novel chemical structure with specific therapeutic or delivery advantages, offering unique treatment efficacy.

2. How does this patent fit into the global patent landscape?
While specific claims are Norwegian, the invention probably aligns with broader European or international patent strategies, with potential for filings under PCT for global protection.

3. Can this patent prevent others from manufacturing similar compounds?
Yes, within Norway and potentially in Europe, if infringement occurs on the claimed compounds or uses, the patent holder can seek legal remedies.

4. What strategies can extend the patent’s commercial lifespan?
Filing supplementary patents for formulations, methods, or new indications can prolong market exclusivity beyond the original expiry.

5. How do prior art references impact this patent’s strength?
If prior art discloses similar compounds or methods, it could limit patent scope; however, the claims’ specificity likely maintain enforceability against close variants.


References

  1. [1] Norwegian Patent Office (NIPO) Patent Database.
  2. [2] European Patent Office (EPO) public databases.
  3. [3] Scientific literature and prior patents cited in the patent family.
  4. [4] International Patent Classification (IPC) related thereto.

(Note: The actual patent documents and legal status should be verified through professional patent databases for the most current insights.)

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