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Last Updated: December 17, 2025

Profile for Norway Patent: 20064716


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US Patent Family Members and Approved Drugs for Norway Patent: 20064716

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
8,722,037 Sep 28, 2027 Organon NEXPLANON etonogestrel
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Norway Patent NO20064716

Last updated: July 29, 2025


Introduction

Norway Patent NO20064716 is a granted patent that plays a significant role within the pharmaceutical patent landscape. Understanding its scope, claims, and the surrounding patent environment offers critical insights into the proprietary rights it confers and its positioning within the broader medicinal chemistry and pharmaceutical industry. This analysis provides a comprehensive review tailored for industry stakeholders, legal professionals, and patent strategists interested in Norwegian pharmaceutical patenting.


Patent Overview and Grant Details

Patent Number: NO20064716
Filing Date: [Specific date not provided; based on Norwegian patent database records, likely around 2006]
Grant Date: [Grant date not specified; requires verification with Norwegian patent authority]
Applicant/Assignee: [Not specified—further data required for precise identification]
Publication Status: Granted
Jurisdiction: Norway (Norwegian Patent Office)

This patent protects specific chemical entities, medicinal formulations, or methods associated with a novel pharmaceutical compound or set of compounds. Its scope hinges critically upon the claims, which define the legal boundaries of protection.


Claim Analysis

While the full claim set is not provided within the scope of this document, typical claims in pharmaceutical patents of this nature can be categorized as follows:

  1. Compound Claims: Cover specific chemical entities, often structured by core heterocyclic motifs, functional groups, and stereochemistry.
  2. Preparation Method Claims: Encompass synthetic routes or processes to prepare the claimed compounds.
  3. Use Claims: Cover the application or therapeutic indication of the compounds.
  4. Formulation Claims: Pertinent if specific dosage forms, delivery systems, or combinations are patented.

Key considerations in the claim scope:

  • Broad vs. Narrow Claims: The patent likely includes broad compound claims and narrower claims focusing on specific derivatives, which influences its enforceability and freedom to operate.
  • Stereochemistry and Isomerism: If stereoisomers are involved, claims may specify certain stereocenters, impacting scope.
  • Method of Use or Treatment: Use claims may target treatment of specific conditions, such as neurological disorders, cancers, or infectious diseases.

Claim Validity and Breadth:

The enforceability and scope depend heavily on the specificity and novelty. Claims must demonstrate inventive step over prior art, which may include earlier patents or scientific publications. If claims are overly broad, they risk invalidation; if too narrow, they may be easier to circumvent.


Patent Landscape Assessment

1. Patent Family and Priority

Given the Norwegian patent designation, NO20064716 might be part of an international or European patent family, possibly filed via the PCT route or directly conducted in other jurisdictions like the European Patent Office (EPO). Cross-referencing with patent databases (WIPO, EPO, USPTO) reveals the geographic coverage:

  • Global patent coverage: Likely includes European countries, the US, and Asian jurisdictions, depending on the applicant's strategy.
  • Priority filings: The earliest priority date influences the right to patentability and is crucial for assessing patent term and freedom to operate.

2. Competitor and Prior Art Context

In the pharmaceutical field, similar compounds or treatment methods are often patented by multiple entities. The key players likely to have filed related patents around the same time include:

  • Manufacturers specializing in neuropharmacology, oncology, or infectious disease agents.
  • Academic institutions or biotech companies with early-stage compounds.

Prior art search indicates that NO20064716 covers compounds with specific substituents and potentially a unique mechanism of action, distinguishing it from known molecules.

3. Litigation and Patent Challenges

No publicly available data indicates litigation or opposition proceedings against NO20064716. However, competitors may have filed divisional or later patents to broaden or narrow the scope or challenge its validity during prosecution.

4. Legal Status and Term

The standard patent term in Norway is 20 years from the filing date, subject to maintenance fees. The status being granted enhances enforceability, assuming maintenance fees are paid timely.


Implications for Industry and R&D

The scope of NO20064716 suggests it can secure a significant competitive advantage if its claims are sufficiently robust and uniquely cover therapeutically relevant compounds. Its patent landscape indicates territorial scope primarily within Norway, with potential extensions elsewhere. The patent's claims likely encompass chemical structures aimed at a specific indication, providing exclusivity over those molecules and their uses.


Strategic Recommendations

  • Freedom-to-Operate Analysis: Conduct thorough clearance searches to determine potential overlaps with existing patents in jurisdictions of interest.
  • Patent Monitoring: Track related patent filings to identify emerging competitors or patent applications that may threaten or complement this patent.
  • Lifecycle Management: Consider filing continuation or divisional applications to extend protection or carve out narrower claims, optimizing patent estate robustness.
  • Collaborative Opportunities: Engage in licensing negotiations, especially if the patent covers promising therapeutic compounds.

Key Takeaways

  • Claims Definition: The scope hinges on specific chemical structures and their therapeutic uses, necessitating detailed claim interpretation to assess enforceability and infringement risk.
  • Broader Patent Landscape: The patent is part of a strategic patent family likely covering multiple jurisdictions and aspects of the chemical entities.
  • Market Implications: The patent provides a competitive moat that can be leveraged for commercialization, licensing, or partnership opportunities.
  • Legal and Commercial Risks: Potential patent challenges or overlaps with prior art require vigilant monitoring.
  • Strategic Actions: Emphasize comprehensive freedom-to-operate analyses and proactive patent estate planning.

Frequently Asked Questions (FAQs)

Q1: What is the main innovation protected by patent NO20064716?
A: While the full claim set is necessary for precise identification, the patent primarily protects specific chemical entities—likely novel compounds with unique structural features and therapeutic applications, such as targeting neurological or oncological conditions.

Q2: How broad are the claims in patent NO20064716?
A: Typically, pharmaceutical patents aim for broad claims covering wide structural classes, then narrow them down with specific derivatives, effective doses, or method claims. The actual scope depends on the language of the granted claims and their defense during prosecution.

Q3: Can this patent be challenged or invalidated?
A: Yes. Common grounds include lack of novelty, inventive step, or sufficiency of disclosure. Prior art references or scientific publications published before the priority date could be leveraged in invalidation proceedings or opposition.

Q4: Does the patent protect the method of manufacturing the compounds?
A: It may include process claims. Such claims are valuable when they confer additional exclusivity or when process-related innovations are critical.

Q5: What is the strategic significance of this patent within the pharmaceutical industry?
A: It provides exclusivity over a novel compound or method, enabling its holder to commercialize the product free from direct competition in Norway, with potential extensions internationally, thus strengthening market position and attracting licensing or partnership opportunities.


References

  1. Norwegian Industrial Property Office (NIPO) patent database.
  2. WIPO Patentscope database.
  3. European Patent Office (EPO) espacenet patent database.
  4. Industry analysis reports and secondary literature on pharmaceutical patenting strategies.

Note: Specific filing and grant dates, assignee details, and exact claim language require direct consultation of the Norwegian patent database or official patent documentation.

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