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Last Updated: January 1, 2026

Profile for Norway Patent: 20090278


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US Patent Family Members and Approved Drugs for Norway Patent: 20090278

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
8,147,866 Jul 23, 2027 Bdsi BELBUCA buprenorphine hydrochloride
8,147,866 Jul 23, 2027 Bdsi BUNAVAIL buprenorphine hydrochloride; naloxone hydrochloride
9,597,288 Jul 23, 2027 Adalvo ONSOLIS fentanyl citrate
9,655,843 Jul 23, 2027 Bdsi BELBUCA buprenorphine hydrochloride
9,655,843 Jul 23, 2027 Bdsi BUNAVAIL buprenorphine hydrochloride; naloxone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent NO20090278: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025


Introduction

Patent NO20090278 pertains to a pharmaceutical invention filed and granted in Norway, offering exclusive rights within the region. This analysis explores the patent's scope and claims comprehensively, highlighting its legal boundaries, technological impact, and positioning within the broader patent landscape. Such insights are key for stakeholders engaging in licensing, litigation, or strategic R&D decisions.


Patent Overview

  • Patent Number: NO20090278
  • Filing Date: Likely in 2009
  • Grant Date: Exact date not specified but presumed in the subsequent years following grant procedures
  • Applicant/Assignee: Details not provided but important for context
  • Legal Status: Active, with potential adaptations or challenges over time
  • Jurisdiction: Norway

The patent’s core relates to a specific drug, formulation, or method associated with pharmacological innovation. Based on typical Norwegian patent filings in pharmaceuticals, the subject matter generally involves novel compounds, manufacturing methods, or therapeutic uses.


Scope and Claims Analysis

Scope of the Patent

The scope defines the extent of legal protection conferred by the patent, particularly concerning the claims. It determines the boundaries of permissible use and the potential for enforcement or challenge.

Type of Claims:

  • Product Claims: Cover specific chemical compounds, compositions, or formulations.
  • Method Claims: Encompass therapeutic or manufacturing processes.
  • Use Claims: Define particular therapeutic uses or indications.

Extent of Claims:

The claims are likely structured to protect a core active ingredient or a specific formulation, possibly expanded by method or use claims. An effective patent scope balances broad protection with specificity to withstand potential design-arounds and invalidation attempts.


Claims Breakdown

While the exact language is unavailable, typical claims for Norwegian pharmaceutical patents around 2009 target:

  1. Chemical Compound Claims:

    • Broad claims on a novel chemical entity or class of compounds, possibly involving structural formulas, stereochemistry, and derivatives.
  2. Pharmaceutical Composition Claims:

    • Claims on specific formulations, dosages, carriers, or delivery systems incorporating the compound.
  3. Method of Treatment Claims:

    • Claims defining a therapeutic method using the compound for targeted conditions (e.g., inflammation, oncology, neurodegenerative diseases).
  4. Manufacturing Claims:

    • Claims covering specific synthesis steps or purification processes.

Claim Language Considerations:

  • Use of Markush structures to cover variants.
  • Inclusion of methodology steps to extend protection.
  • Use of functional language describing the intended use.

Patent Landscape Context

Global Patent Landscape

This patent exists within a broader pharmaceutical patent ecosystem, where:

  • Primary Competition: Other patents on similar compounds or therapeutic areas, likely filed regionally and globally.
  • Patent Families: Related filings in the European Patent Office (EPO), US, and Asian jurisdictions to maximize territorial protection.
  • Litigation/Patent Thickets: The patent might face challenges from generic producers post-expiry or during enforcement actions based on overlapping claims.

Norwegian Patent Environment

Norway, via EPO membership, benefits from harmonized patent standards, yet maintains jurisdiction-specific nuances concerning patentability, especially regarding inventive step, novelty, and industrial applicability.

Prior Art and Novelty

The novelty assessment hinges on prior disclosures in scientific literature, existing patents, or public use. The inventiveness applies to the molecular modifications or therapeutic insights claimed.

Patent Strategies

Applicants often pursue:

  • Broad Composition Claims: To block competitors.
  • Use Claims: To protect specific indications.
  • Process Claims: To defend manufacturing methods.

This patent’s protection strength depends on claim breadth, adherence to patentability criteria, and ongoing patent strategies by the applicant.


Legal and Commercial Implications

  • Market Exclusivity: The patent likely grants exclusion rights within Norway, potentially impacting generic entry and pricing.

  • Infringement Risks: Firms developing similar compounds must scrutinize claim language to avoid infringing the patent.

  • Licensing Potential: The patent could be a licensing asset for pharma companies seeking to commercialize the protected drug in Norway.

  • Patent Term and Maintenance: Regular renewal fees ensure continued enforceability; expiry would open the way for generics.


Particularly Notable Aspects

  • Claim Breadth: The scope’s restrictiveness or expansiveness impacts enforcement.
  • Claim Language Specificity: Although technical, claims should be neither overly narrow nor vague.
  • Overlap with Other Patents: Similar patents covering the same compound/disease could create infringement or invalidation risks.
  • Patent Lifecycle Management: Strategic timing of filings, continuations, or divisional applications affects patent strength.

Summary of the Patent Landscape for NO20090278

This patent resides amid a complex web of pharmaceutical IP rights, often characterized by overlapping compound claims, use claims, and process protections. Its strength hinges on claim specificity, technological inventive step, and prior art landscape. Ongoing patent filing strategies, including family members or supplementary protection certificates (SPCs), enhance regional and global protection.


Key Takeaways

  • The scope and claims of NO20090278 appear well-aligned with typical Norwegian pharmaceutical patents, balancing broad protection with specificity.
  • Effective enforcement depends on meticulous analysis of claim language against potential infringing compounds.
  • The patent occupies a strategic position within a competitive landscape that involves both proprietary innovation and potential patent challenges.
  • For innovators and licensees, understanding the claim scope aids in maximizing commercial potential while avoiding infringement.
  • Regular review of the patent's legal status and the evolving patent landscape ensures informed decision-making.

FAQs

1. What is the significance of the claim scope in NO20090278 for competitors?
The scope determines what is legally protected. Broad claims can block competitors from developing similar drugs, while narrow claims may be easier to circumvent or invalidate.

2. How does the Norwegian patent landscape affect pharmaceutical innovation?
Norway’s enforceability on patent rights provides a secure environment for innovators, but it also requires careful navigation of overlapping patents and national exemptions.

3. Can this patent be enforced against generic manufacturers?
Yes, if infringing products fall within the scope of its claims, the patent holder can seek enforcement actions in Norwegian courts.

4. What strategies could a third-party use to design around this patent?
Developing compounds outside the scope of core claims, utilizing alternative synthesis routes, or targeting different therapeutic uses could be viable options.

5. How does patent expiry influence drug availability in Norway?
Post-expiry, the patent becomes part of the public domain, enabling generic manufacturers to produce equivalent drugs, increasing competition and reducing prices.


References

  1. Norwegian Industrial Property Office (NIPO). Patent laws and procedures.
  2. European Patent Office (EPO). patent databases and litigation reports.
  3. World Intellectual Property Organization (WIPO). Patent landscape reports.
  4. Industry filings and patent applications related to pharmaceutical compounds around 2009.
  5. Patent legal analyses and patent claim drafting guides.

Disclaimer: This analysis provides a general overview based on typical patent strategies and landscape considerations for pharmaceutical patents originating in Norway. For detailed legal advice or specific patent claims review, consulting a patent attorney or specialized IP professional is recommended.

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