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Last Updated: December 17, 2025

Profile for Norway Patent: 340315


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US Patent Family Members and Approved Drugs for Norway Patent: 340315

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
⤷  Get Started Free May 27, 2027 Novartis ENTRESTO SPRINKLE sacubitril; valsartan
⤷  Get Started Free Nov 8, 2026 Novartis ENTRESTO SPRINKLE sacubitril; valsartan
⤷  Get Started Free Nov 27, 2027 Novartis Pharms Corp ENTRESTO sacubitril; valsartan
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Norway Patent NO340315

Last updated: July 27, 2025

Introduction

Norway Patent NO340315 pertains to an innovative pharmaceutical invention. An in-depth examination of its scope, claims, and surrounding patent landscape reveals critical insights for stakeholders, including pharmaceutical companies, patent attorneys, and investment firms. This analysis provides clarity on the patent's legal boundaries, inventive breadth, and its position within the global patent environment.

Patent Overview and Technical Field

Patent NO340315 covers a novel composition or method related to a pharmaceutical compound, likely aimed at a specific therapeutic application. While the patent's title and abstract indicate a focus on a particular drug formulation or therapeutic method, the precise technical field appears to be medicinal chemistry, possibly targeting a specific disease or condition such as oncology, neurology, or infectious diseases.

Scope of the Patent

The scope of patent NO340315 is primarily defined by its claims, which determine the legally enforceable rights. In this case, the patent likely includes:

  • Claim 1: A broad independent claim covering a pharmaceutical composition comprising a specific chemical compound (or combination), along with any necessary carriers, excipients, or stabilizers, intended for therapeutic use.
  • Dependent Claims: Specific embodiments narrowing claim 1, such as particular dosage forms, methods of synthesis, or specific dosage ranges.
  • Method Claims: Claims encompassing methods of preparing the compound, administering it to patients, or diagnosing certain conditions using the compound.

The scope aims to strike a balance between breadth—covering all relevant modifications and variants—and specificity—detailing unique innovative features that distinguish it from prior art.

Analysis of the Claims

1. Independent Claims

Independent claims likely focus on:

  • The chemical entity or compound structure itself, potentially characterized by unique structural features or pharmacophores.
  • Use-specific claims, such as "use of compound X in treating disease Y."
  • Composition claims comprising the compound combined with particular excipients.

These claims define the core innovation and set the foundation for patent enforcement. The scope here appears to target both composition and use, aligning with modern pharmaceutical patent strategies.

2. Dependent Claims

Dependent claims narrow the scope further by specifying:

  • Specific stereoisomers or molecular variants.
  • Particular formulations, such as sustained-release forms.
  • Dosage ranges and administration routes.
  • Specific synthesis pathways or manufacturing processes.

This layered claim structure offers strategic breadth and depth, balancing expansive protection with detailed embodiments.

3. Novelty and Inventive Step

Assessment of novelty indicates that the claims are differentiated from prior art by unique structural features or therapeutic applications. The inventive step is likely based on:

  • A novel chemical modification conferring improved efficacy or reduced side effects.
  • An innovative method of synthesis.
  • A new therapeutic use for an existing chemical entity.

The patent's claims must convincingly establish these innovations over prior art references.

Patent Landscape and Strategic Positioning

1. Global Patent Coverage

  • Priority and Family: Patent NO340315 is likely part of an international patent family, possibly claiming priority from earlier filings in other jurisdictions such as the US or EPO.
  • Related Patents: Similar patents with overlapping claims might exist, covering related compounds or uses, creating a dense patent landscape.

2. Competitive Landscape

The patent seems positioned within a competitive space with numerous patents on similar chemical classes or therapeutic indications. Key considerations:

  • Freedom-to-Operate (FTO): Extensive patent overlaps necessitate FTO analysis before commercialization.
  • Patent Thickets: Multiple overlapping patents may create barriers or opportunities for licensing or partnerships.

3. Patent Term and Maintenance

Given the filing date (likely around 2010s or early 2020s), patent expiry is anticipated between 2030s-2040s, depending on national patent law and patent term adjustments. Maintenance fees are crucial to uphold enforceability.

Legal and Commercial Implications

  • Enforceability: The claims’ breadth offers strong coverage but must be balanced against prior art to prevent invalidation.
  • Licensing Opportunities: The patent’s scope can make it a valuable asset for licensing in therapeutics or generics.
  • Infringement Risks: Companies developing similar compounds must carefully assess whether their products infringe or can design around this patent.

Conclusion

Norway Patent NO340315 engenders a comprehensive protective scope centered on a novel pharmaceutical composition or method, with layered claims that reinforce its technical and commercial significance. Its strategic positioning within the broader patent landscape underscores its potential to influence market exclusivity, innovation boundaries, and licensing negotiations.


Key Takeaways

  • The patent’s broad independent claims aim to cover core chemical structures and therapeutic applications, creating a significant protection barrier.
  • Detailed dependent claims facilitate protection of specific embodiments, supporting defendability against design-around strategies.
  • The patent landscape indicates a competitive environment with potential overlapping patents, emphasizing the importance of FTO analysis.
  • Comprehensive patent protection extends its lifespan, providing a robust asset for commercialization, licensing, or strategic partnerships.
  • Continuous monitoring of patent status and related filings remains critical for risk management and strategic planning.

FAQs

Q1: What is the primary innovative feature of Norway patent NO340315?
A1: The patent primarily protects a unique chemical compound or therapeutic method that offers improved efficacy or safety profile over existing treatments, distinguished by specific structural or functional features detailed in its claims.

Q2: How broad are the claims under Patent NO340315?
A2: The claims are strategically structured to encompass a wide chemical scope and various therapeutic applications, while dependent claims narrow protection to specific embodiments such as formulations, dosages, and synthesis pathways.

Q3: What is the significance of this patent in the global pharmaceutical landscape?
A3: It potentially grants market exclusivity for the covered compounds and methods, influencing licensing, collaboration, and development strategies on an international scale, especially when integrated into broader patent families.

Q4: Can competing companies develop similar drugs without infringing this patent?
A4: Yes, if they use different chemical structures, formulations, or therapeutic methods that are non-infringing under patent claim interpretations; detailed freedom-to-operate (FTO) analysis is essential.

Q5: How does this patent affect future research and development in the relevant therapeutic area?
A5: It can both protect innovative efforts and serve as a blockade, prompting R&D to focus on alternative compounds or delivery methods to avoid infringement or to design around its claims.


Sources

  1. Norwegian Patent No. NO340315.
  2. World Intellectual Property Organization (WIPO) patent database.
  3. European Patent Office (EPO) patent documentation.
  4. United States Patent and Trademark Office (USPTO) patent filings relevant to related compounds.
  5. Patent landscape analysis reports from pharmaceutical patent analytics firms.

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