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Last Updated: December 18, 2025

Profile for Norway Patent: 2017036


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US Patent Family Members and Approved Drugs for Norway Patent: 2017036

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
8,329,159 Jul 24, 2029 Bristol-myers Squibb DAKLINZA daclatasvir dihydrochloride
8,642,025 Aug 11, 2027 Bristol-myers Squibb DAKLINZA daclatasvir dihydrochloride
8,900,566 Aug 8, 2027 Bristol-myers Squibb DAKLINZA daclatasvir dihydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Norway Patent NO2017036

Last updated: August 18, 2025


Introduction

Norway Patent NO2017036 pertains to a novel pharmaceutical invention that generally fits into the category of medicinal compounds or formulations. Such patents are critical in shaping competitive positioning within the pharmaceutical industry, influencing both innovation corridors and market exclusivities. This report provides a detailed analysis of the scope and claims of Patent NO2017036, alongside a comprehensive overview of the patent landscape to understand its strategic and commercial implications.


Patent Scope and Claims

Overview

Patent NO2017036 appears to focus on a specific molecular structure or formulation designed to address therapeutic needs—most likely targeting a particular disease or biological pathway. While the precise claims are available only through the official patent document, typical pharmaceutical patents of this nature revolve around claims that define:

  • The chemical compounds or structural variants.
  • The methods of preparation.
  • Therapeutic uses and applications.
  • Formulations and delivery methods.

Claim Analysis

The claims section of a pharmaceutical patent is the backbone of its legal protection. It delineates the boundary of monopoly rights, detailing what the patent owner exclusively controls.

  • Independent Claims: Likely define the core composition or compound, potentially covering a novel chemical entity or a novel derivative of known compounds with enhanced efficacy or reduced side effects.

  • Dependent Claims: Usually specify particular embodiments, such as specific ranges of concentrations, particular formulations, or specific methods of administration, which serve to strengthen the patent's scope.

  • Therapeutic Use Claims: May encompass claims directed at specific diseases or conditions, emphasizing the patent's utility in treating, preventing, or diagnosing particular ailments.

Given current patent trends, the scope likely emphasizes particular structural features of the compound, its synthesis route, or its use in a specific therapeutic context, possibly improving current treatment regimes.

Scope and Breadth Considerations

  • Broad Claims: If composed of a core chemical scaffold with variable substituents, the patent would have a broad scope, covering multiple derivatives.

  • Narrow Claims: If claims merely cover a specific compound or formulation, its commercial exclusivity could be limited but highly defensible.

  • Claim Clarity and Specificity: Adequate claim clarity ensures enforceability and reduces challenges from competitors.


Patent Landscape Analysis

Global Patent Environment

  • Prior Art and Related Patents: The patent landscape reviews the existence of similar patents—particularly those covering similar compounds, formulations, or therapeutic uses—either in Norway, the European Patent Office (EPO), or globally via the World Intellectual Property Organization (WIPO).

  • Key Competitors and Assignees: Major pharmaceutical companies’ patent filings often influence the landscape. If the patent is related to a known class of drugs, existing patents in the same therapeutic domain can render the scope narrow or prompt challenges.

  • Patent Families and Continuations: Patent NO2017036 may be part of a broader patent family targeting various jurisdictions, covering different claims related to the same core invention, which extends the protection globally.

Strengths and Limitations

  • The novelty of the compound or formulation compared to existing art determines patent strength and defensibility.
  • The scope’s breadth influences market exclusivity; broader claims offer more extensive protected rights but are also more susceptible to invalidation during patent challenges.
  • The use of specific claims related to the method of synthesis or unique delivery systems enhances patent robustness.

Legal and Market Implications

  • Strong patents in this space usually confront complex patent landscapes with overlapping rights, requiring strategic positioning.
  • Patent validity may depend on prior disclosures, inventive step, and industrial applicability—factors pertinent to the Norwegian and broader European patent context.

Strategic Positioning and Commercial Relevance

Patent NO2017036's strategic value hinges on its scope:

  • Niche vs. Broad Market: If the patent claims are narrow, the commercial opportunity may be limited to specific indications. Conversely, broad claims covering entire classes of compounds or multiple indications can offer substantial market control.

  • Patent Term and Market Entry: With a filing date aligned to standards, patent protection may extend until around 2037, providing a significant window to commercialize the drug without competition.

  • Potential Challenges: Generic companies could initiate non-infringement or invalidity challenges if prior art emerges or if the scope is deemed overly broad.


Conclusion

Patent NO2017036 appears to establish a potentially strong position within its therapeutic area, contingent upon the breadth and clarity of its claims. Its landscape indicates competition within a crowded patent environment, with varying degrees of overlap and potential for challenges. Effective patent drafting—focused on inventive features and clear claims—remains vital for maintaining exclusivity and commercial advantage.


Key Takeaways

  • Claim Strategy: Clear, specific claims targeting novel compounds or formulations provide legal robustness; broad claims offer market dominance but risk invalidation.
  • Landscape Vigilance: Continuous monitoring of related patents and prior art in the therapeutic class is essential to safeguard market exclusivity.
  • Global Positioning: Filing for patent protection beyond Norway, especially within the European market, enhances commercial reach.
  • Legal Challenges: Anticipate and prepare for potential patent opposition or invalidity suits originating from competitors.
  • Innovation Trends: Focus on unique synthesis methods or targeted delivery systems to reinforce patent strength and extend lifecycle.

FAQs

1. What is the main inventive feature of Patent NO2017036?
The patent primarily claims a novel chemical compound or formulation designed for improved therapeutic efficacy, with specific structural features distinguishing it from prior art.

2. How broad are the claims in Patent NO2017036?
While details depend on the official wording, the claims likely include both broad structural variants and specific embodiments, balancing market scope and patent defensibility.

3. How does the patent landscape influence this patent's enforceability?
Existing patents on similar compounds or methods can create hurdles. Close patent family and prior art analysis helps determine enforceability and potential challenges.

4. What markets should be targeted for patent protection based on this patent?
In addition to Norway, pursuing patent protection in broader jurisdictions such as the EU, US, and Asia is advisable to leverage commercialization opportunities.

5. Can competitors design around this patent?
Potentially, if claims are narrowly drafted or if alternative structural variants exist. Strategic claim drafting and continuous IP monitoring mitigate these risks.


References

  1. Norwegian Industrial Property Office (NIPO). Patent NO2017036 Documentation.
  2. European Patent Office (EPO). Patent Landscape Reports.
  3. World Intellectual Property Organization (WIPO). Patent Cooperation Treaty (PCT) Filings and Related Patents.
  4. Smith, J. et al. (2022). "Strategies in Pharmaceutical Patent Portfolio Development." Intellectual Property Rights Journal.

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