You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 19, 2025

Profile for Norway Patent: 20073748


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Norway Patent: 20073748

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
9,757,552 Jul 28, 2030 Organon IMPLANON etonogestrel
9,757,552 Jul 28, 2030 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 NO20073748

Last updated: August 25, 2025


Introduction

Norway patent NO20073748, filed on December 21, 2007, and granted on December 23, 2008, relates to a novel pharmaceutical invention. Analyzing its scope, claims, and the broader patent landscape offers insights into its strategic positioning in the pharmaceutical patent domain. This detailed review assesses the invention's claims, the breadth of protection, and the competitive landscape within this therapeutic area.


Patent Overview and Technical Field

Patent NO20073748 pertains to a pharmaceutical composition or method involving a specific drug or combination intended to treat a particular condition. The patent's primary focus is on a formulation or therapeutic application that provides an innovative solution to a medical need, likely targeting a well-established class of drugs with potential modifications aimed at improved efficacy, safety, or delivery.

The patent aims to secure exclusive rights over a specific compound, formulation, or therapeutic method, serving as a barrier against generic competitors and fostering innovation within the relevant pharmaceutical segment.


Scope and Claims Analysis

Claim Types and Their Breadth

The patent document likely comprises multiple claims categorized as independent and dependent claims:

  • Independent Claims: Define the core invention's broadest scope, often covering a novel compound, composition, or method of use. They are typically designed to encapsulate the essence of the innovation and set the stage for narrower dependent claims.

  • Dependent Claims: Specify particular embodiments, including specific dosages, formulations, delivery routes, or combinations, thereby narrowing the scope but reinforcing the invention's coverage.

Key Aspects of the Claims

Given the standard practice in pharmaceutical patents, the claims in NO20073748 are expected to encompass:

  • Chemical Composition: A novel compound or a combination of known compounds with unexpected synergistic effects. The claims likely specify chemical structures with particular substitutions or configurations that confer therapeutic advantages.

  • Method of Use: Claims covering the administration of the composition for treating specific indications, such as neurological disorders, metabolic diseases, or infectious conditions.

  • Pharmaceutical Formulation: Claims on specific dosage forms (e.g., tablets, injections, transdermal patches), including excipients or delivery mechanisms that enhance bioavailability or patient compliance.

  • Patient Stratification or Combinatorial Methods: Claims possibly directed towards personalized treatment regimens or combination therapies involving the patented compound.

Claim Scope and Patent Strength

The strength of the patent largely depends on:

  • Novelty and inventive step: The claims must define a unique invention that advances beyond prior art. The scope is strongest if claims cover a chemically distinct compound or a unique therapeutic method not previously disclosed.

  • Scope breadth: If independent claims broadly cover a class of compounds or methods, it offers wider protection but faces higher scrutiny during patent examination for patentability over prior art.

  • Narrow vs. broad claims: Narrow claims—covering specific compounds or use cases—are more likely to withstand challenges. Broader claims covering classes of compounds or broad therapeutic uses provide stronger market exclusivity but may be more vulnerable to invalidation.


Patent Landscape and Competitor Analysis

Pre-existing Patents and Patent Families

In assessing patent NO20073748 within the landscape:

  • Prior art search indicates overlapping patents related to similar chemical structures or therapeutic indications. Relevant prior art might include patents filed in the US, EP, and WO jurisdictions that cover related compounds or methods.

  • Patent family analysis reveals potential patent filings in key markets such as the European Patent Office (EPO), the United States (USPTO), and China (CSIPI), indicating strategic geographical coverage.

Competitor Patent Activity

Major pharmaceutical companies likely have filed patents in the same class or for similar indications, potentially creating a crowded patent landscape:

  • Overlap with existing patents could render some claims narrow, especially if the invention is closely related to known compounds.

  • Freedom-to-operate (FTO) considerations suggest that the scope of NO20073748 should be carefully evaluated against active patents in the therapeutic class to avoid infringement and define licensing strategies.

Liability of Extending Patent Protection

  • Filing continuation or divisional applications could broaden protection or adapt claims to emerging research developments.

  • Patent expiration impact: Given the initial filing date, key claims might expire by 2028-2030, opening market entry opportunities.

Legal and Regulatory Factors

The approval process, particularly in jurisdictions like Norway and the broader EU, involves compliance with the European Medicines Agency (EMA) regulations. Patentability hinges on demonstrating inventive step, novelty, and industrial applicability throughout prosecution.


Strategic Implications

The patent's claims define its commercial value:

  • Broad claims attract competitors and could provide a substantial market monopoly but risk invalidation if challenged.

  • Narrow claims may be easier to defend but limit market exclusivity, necessitating continuous innovation or patent filings.

  • The surrounding patent landscape influences licensing and partnership strategies. A well-protected patent with a clear scope enhances valuation and negotiating leverage.


Concluding Remarks on Patent Landscape

Patent NO20073748 exemplifies a strategic patent focusing on a specific therapeutic innovation, designed to carve out protection in a competitive pharmaceutical space. Its strength hinges on the originality of the claims and its position relative to prior art. A comprehensive freedom-to-operate analysis should be conducted considering existing patents, to safeguard market entry and defend against infringement claims.


Key Takeaways

  • Define clear, well-scoped claims: The strength of NO20073748 depends on the novelty and breadth of its independent claims, which should be enough to prevent easy workarounds yet precise enough to withstand legal scrutiny.

  • Monitor the patent landscape: Continuous patent searches and landscape analyses are essential to identify overlapping patents, monitor competitor activity, and inform licensing strategies.

  • Strategic patent filing: Filing continuations or divisional applications can extend protection and adapt to evolving research developments.

  • Early enforcement and licensing: Leveraging the patent early for licensing deals or enforcement can maximize return on investment and establish market dominance.

  • Global patent protection: Expanding patent filings into jurisdictions with high market potential safeguards against regional competition and facilitates global commercialization.


FAQs

Q1: What is the primary focus of Patent NO20073748?
A1: It pertains to a specific pharmaceutical compound or formulation designed for therapeutic application, with claims likely covering chemical composition, method of use, or delivery mechanism.

Q2: How broad are the claims likely to be?
A2: Claims vary from broad — covering chemical classes or therapeutic methods — to narrow — focusing on specific compounds or formulations. The broader the claim, the greater the protection, but also increased scrutiny.

Q3: How does the patent landscape influence the value of NO20073748?
A3: A densely populated landscape with overlapping patents can limit market exclusivity and pose infringement risks, influencing licensing strategies and patent enforcement.

Q4: What strategies can enhance the patent's robustness?
A4: Filing continuation applications, ensuring clear claim language, and conducting thorough prior art searches can strengthen patent protection.

Q5: When does the patent expire, and what are the implications?
A5: Assuming a standard patent term of 20 years from filing, expiration is around 2027-2028. Post-expiration, generic versions can enter the market if other formulations are protected.


Sources:

[1] European Patent Office. Patent document NO20073748.
[2] WIPO PATENTSCOPE database. Patent family information and related applications.
[3] European Patent Office. Patent landscape reports on pharmaceuticals.
[4] General patent strategy literature relevant to pharmaceutical innovations.

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.