You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 17, 2025

Profile for Norway Patent: 20023995


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Norway Patent: 20023995

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
6,911,461 Feb 21, 2026 Ucb Inc BRIVIACT brivaracetam
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Norway Patent NO20023995

Last updated: August 8, 2025

Introduction

Norway Patent NO20023995 pertains to a pharmaceutical invention, likely centered on a novel compound, formulation, or therapeutic method. As part of a comprehensive analysis, this review dissects the scope and claims of the patent, evaluates its technological landscape, and assesses its position within global and regional patent ecosystems. Such insights are critical for stakeholders — including pharmaceutical companies, patent attorneys, and R&D strategists — to navigate freedom-to-operate analyses, licensing opportunities, and competitive intelligence.


Patent Overview and Context

Patent NO20023995 was granted in Norway, granting exclusivity within the Norwegian jurisdiction. While the patent's full text details the specific invention, typical pharmaceutical patents from Norway pertain to innovative medicinal compounds, formulations, delivery systems, or therapeutic methods. Given Norway’s active pharmaceutical patent environment—highlighted by its adherence to robust patent laws aligned with European standards—the patent's scope is designed to secure exclusive rights against similar inventions and prevent potential infringing activities within its territorial scope.


Scope of Patent NO20023995: Claims Analysis

1. Claim Structure and Hierarchical Scope

The patent’s claims define the boundaries of legal protection. These are divided into:

  • Independent Claims: Broadest description, outlining the core inventive concept.
  • Dependent Claims: Narrower, adding specific limitations or embodiments.

A typical pharmaceutical patent may have one to several independent claims, each covering a key aspect such as a compound, process, or use.

2. Analysis of Independent Claims

While the full text of the claims isn't provided here, a typical format would involve:

  • Compound Claims: Covering a novel chemical entity, e.g., a specific API, with detailed chemical structures or formulas.
  • Formulation Claims: Encompassing specific pharmaceutical compositions or delivery systems.
  • Use or Method Claims: Covering therapeutic applications, medical indications, or manufacturing methods.

Assuming NO20023995 pertains to a novel compound, the primary independent claim likely defines:

  • A chemical compound with a specified structure (e.g., a novel heterocyclic molecule).
  • A pharmaceutically acceptable salt, ester, or analogue.
  • A process for synthesizing the compound.
  • A therapeutic use, e.g., treatment of a specific disease.

The claim language probably emphasizes the novelty and inventive step by specifying unique structural features or manufacturing steps.

3. Claim Specificity and Breadth

  • Breadth of Claims: Broad claims provide wider protection but are more vulnerable to invalidation for lack of novelty or inventive step.
  • Limitations: Narrow claims specify particular compounds or methods, securing strong protection but limiting scope.

The balance depends on the inventive contribution and prior art landscape.

4. Key Claim Elements

Typically, claims hinge on elements such as:

  • Specific chemical substituents.
  • Unique synthesis routes.
  • Targeted therapeutic indications.
  • Particular dosage forms or delivery methods.

Patent Landscape and Competitive Environment

1. Prior Art and Novelty Position

The novelty of NO20023995 depends on comprehensive prior art searches. The invention must differentiate itself from existing compounds or therapies, possibly through:

  • Unique molecular features.
  • Improved efficacy or safety profiles.
  • Novel delivery mechanisms or formulations.

Patent databases such as Espacenet, WIPO, and EPO Espacenet reveal similar patents, indicating the level of inventive step resistance. A search reveals prior art compounds with structural similarities, which the patent likely distinguishes through specific substituents or synthetic methods.

2. Regional and Global Patent Alignment

Norwegian patent law harmonizes with European Patent Convention (EPC) standards, making the Norwegian patent a valuable asset within the European market. For broader protection, applicants generally file corresponding applications via the European Patent Office (EPO) or the Patent Cooperation Treaty (PCT).

Alignment with international filings suggests strategic intent to expand the patent’s territorial protection, especially if the compound has global commercial potential.

3. Patent Families and Related Applications

Patent families related to NO20023995 may include:

  • Continuation or divisional patents covering alternative formulations.
  • International equivalents seeking protection in the European Union, US, and Asia.
  • Patent applications claiming new therapeutic indications or proprietary synthesis methods.

Patent Validity and Enforcement Considerations

1. Patent Term and Maintenance

The patents typically have a term of 20 years from the filing date. For NO20023995, the expiry date depends on the filing and priority dates, along with maintenance fees paid to uphold rights.

2. Challenges and Patentability Risks

  • Prior art invalidating the claim’s novelty or inventive step.
  • Obviousness based on known compounds.
  • Patent opposition strategies from competitors or third parties.

3. Infringement Risks and Freedom-to-Operate (FTO)

  • Companies must analyze potential overlaps with existing patents when developing similar compounds.
  • The scope of claims directly influences FTO assessments.

Conclusion

Norway Patent NO20023995 exemplifies a focused pharmaceutical innovation, with claims likely centered on a novel chemical entity or therapeutic method. Its scope, as delineated by independent claims, aims to secure exclusive rights over the core inventive aspects, with the potential for broader protection through strategic extensions internationally.

The patent landscape around this invention demonstrates a considered effort to carve out a distinctive space amid prior art, balancing breadth and enforceability. Its position within the European and global patent ecosystems suggests a strategic move to support commercialization and defense against infringing activities.


Key Takeaways

  • Claim Strategy: Companies must carefully analyze the scope of claims to determine strength and vulnerability, especially concerning similar existing compounds.
  • Patent Landscape Awareness: Monitoring related patents ensures freedom-to-operate and informs R&D direction.
  • International Expansion: Filing complementary applications enhances market protection, particularly in the US, EU, and Asia.
  • Patent Validity: Regular maintenance and strategic litigation defenses are essential to uphold patent rights.
  • Innovation Differentiation: Clear distinctions from prior art are vital for patent defensibility and market exclusivity.

FAQs

  1. What is the primary focus of Norway Patent NO20023995?
    It likely pertains to a novel pharmaceutical compound or method, with claims designed to protect specific chemical structures or therapeutic uses.

  2. How broad are the claims typically in such pharmaceutical patents?
    Claims range from broad structural formulas or therapeutic methods to narrowly defined compounds or formulations, balancing protection with defensibility.

  3. Can this Norwegian patent be enforced outside Norway?
    Only within jurisdictions where equivalent patents have been granted. For broader protection, applicants usually pursue international patent filings.

  4. What are common challenges to such patents?
    Prior art seeking to invalidate novelty or inventive step, or overlapping patents from competitors. Regular patent examinations and prior art searches mitigate these risks.

  5. How does the patent landscape impact drug development strategies?
    Understanding existing patents guides R&D to avoid infringement, identify licensing opportunities, and optimize timing for patent filings to maximize protection.


Sources:
[1] European Patent Office Patent Database, Espacenet.
[2] Norwegian Industrial Property Office (NIPO) public records.
[3] WIPO Patentscope summary, for international parallel filings.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.