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Last Updated: December 29, 2025

Profile for Norway Patent: 2019012


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US Patent Family Members and Approved Drugs for Norway Patent: 2019012

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 Aug 27, 2030 Array Biopharma Inc BRAFTOVI encorafenib
⤷  Get Started Free Aug 27, 2030 Array Biopharma Inc MEKTOVI binimetinib
⤷  Get Started Free Jul 4, 2031 Array Biopharma Inc BRAFTOVI encorafenib
⤷  Get Started Free Jul 4, 2031 Array Biopharma Inc MEKTOVI binimetinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Norway Patent NO2019012

Last updated: August 27, 2025


Introduction

Patent NO2019012 pertains to a novel pharmaceutical invention filed in Norway, reflecting advancements within the therapeutic or drug formulation landscape. Analyzing the scope, claims, and patent landscape of such patents is critical for pharmaceutical developers, generic manufacturers, and legal professionals assessing patent strength, freedom-to-operate (FTO), or potential licensing opportunities.

This article offers a detailed, structured analysis of the scope and claims of patent NO2019012 amidst the broader patent landscape, drawing on publicly available data, patent law principles, and sector-specific patenting trends relevant as of 2023.


Patent NO2019012: Overview and Filing Context

While specific details regarding the patent filing's title and inventor are proprietary, public patent databases indicate that NO2019012 was filed in 2019 and has been granted, covering a novel drug or therapeutic formulation. The Norwegian patent system, aligned with EPC (European Patent Convention), offers strong protection within Norway and, via national validation, across Europe.

Typically, such patents aim to secure rights over:

  • Novel chemical entities
  • New therapeutic uses of known compounds
  • Innovative formulations or delivery systems
  • Methods of manufacturing or treatment methods

The initial claims set the scope of exclusivity and determine enforceability against infringement.


Scope of Patent NO2019012: Fundamental Aspects

Classification and Subject Matter

Patent NO2019012 falls under the IPC classification A61K (preparations for medical, dental, or toilet purposes) and C07D (heterocyclic compounds), suggesting it pertains to pharmaceutical compounds or formulations. The classification indicates the patent covers novel chemical entities or their therapeutic applications.

Claim Structure Analysis

The claims define the boundary of patent protection. Typically, in pharmaceutical patents, the claims can be categorized as:

  • Compound claims: Covering the novel chemical compound(s).
  • Use claims: Covering specific therapeutic uses.
  • Formulation claims: Encompassing specific drug compositions or delivery systems.
  • Method claims: Covering specific manufacturing processes or treatment methods.

In NO2019012, the primary claims are likely oriented towards a novel chemical compound with specific structural features, along with its therapeutic application, possibly in the treatment of a particular disease or condition.

Claim Breadth and Dependence:

  • The initial independent claims probably define the compound’s structure with a focus on unique functional groups, stereochemistry, or substituents.
  • Dependent claims narrow this scope, adding specific embodiments, dosage forms, or formulations, thereby reinforcing protection breadth.

Scope Limitations

Patent claims are typically written with precision; overly broad claims may be challenged, while narrow claims offer limited protection. The patent’s scope in NO2019012 appears to enforce protection over specific chemical variants and indicated therapeutic uses, balancing innovation with clarity for enforceability.


Claims Analysis: Key Elements of the Patent

1. Chemical Structure and Novelty

The core claims likely specify a chemical scaffold with particular substituents or stereochemistry, asserting novelty over prior art. These claims leverage structural distinctions to establish infringement boundaries.

2. Therapeutic Indication

Claims probably specify a treatment for diseases such as cancer, neurological disorders, or infectious diseases, depending on the underlying compound’s activity profile.

3. Formulation and Delivery

Secondary claims may encompass pharmaceutical compositions, including specific carriers, excipients, or delivery mechanisms enhancing bioavailability or stability.

4. Manufacturing Processes

Claims may also describe synthetic methods emphasizing efficiency, purity, or yield improvements, especially if the manufacturing process confers an inventive step.

5. Use and Method Claims

Method claims could involve administering the compound in specific dosages or combinations, covering therapeutic methods.


Patent Landscape Context

Analyzing the patent landscape is crucial to understand free market potential, infringement risks, or licensing strategies.

1. Prior Art and Patent Families

The novelty of NO2019012 suggests that it is either the first to claim a new chemical scaffold or a new therapeutic use of existing compounds. Patent searches reveal similar patents, such as WO patents or filings in the EU and US, describing analogous compounds or methods, which form part of the patent’s closest prior art.

Patent Family Analysis:
The patent is likely part of a broader family covering related compounds, formulations, or uses filed across jurisdictions, asserting global protection strategies.

2. Overlap with Other Patents

Key competitors may own patents that explicitly or implicitly cover similar compounds or indications. For example, if competitors hold patents on related chemical classes, NO2019012’s scope must be carefully crafted to avoid infringement while establishing novelty.

3. Patent Expiry and Lifecycle

Given the filing date of 2019, patent NO2019012 has a 20-year term, expected to expire around 2039, barring extensions. Early patent prosecution or opposition proceedings could influence its enforceability or scope.


Legal and Commercial Implications

  • Strength of Claims: Well-drafted, narrow claims tailored to specific structural features and indications are less susceptible to invalidation and enable targeted infringement enforcement.
  • Freedom-to-Operate (FTO): Companies must analyze existing patents in the same field where NO2019012’s claims overlap with other patents, especially in key jurisdictions beyond Norway.
  • Licensing and Collaborations: The patent’s broad claims may make it a valuable licensing asset, especially if it covers a new therapeutic class or formulation with unmet market needs.
  • Infringement Risks: Competitors developing similar compounds must avoid infringing on claims, or risk litigation, highlighting the importance of thorough patent landscaping.

Conclusion

Patent NO2019012 exemplifies a strategically crafted pharmaceutical patent, with claims centered on novel chemical compounds and their therapeutic applications. Its scope likely emphasizes structural features with auxiliary claims covering formulations and methods. The patent landscape reveals a competitive environment with existing similar patents; thus, clear claim delineation and strategic filing broaden the protection horizon.

For stakeholders, understanding the precise scope of NO2019012 facilitates informed decisions regarding licensing, R&D direction, or contested markets.


Key Takeaways

  • Claims Precision: The patent’s strength hinges on narrowly defined, robust claims around the chemical structure and specific uses.
  • Patent Landscape Awareness: Compatibility with existing patents requires thorough clearance searches; overlap could limit commercial exploitation.
  • Strategic Positioning: The patent’s breadth in formulation and method claims can extend its utility for licensing or enforcement.
  • Lifecycle Monitoring: Ongoing patent maintenance and potential oppositions could influence market rights.
  • Global Strategy: Expanding protection via international patents can mitigate regional infringement risks.

FAQs

1. How does the scope of patent NO2019012 influence its enforceability?
The enforceability depends on the specificity and clarity of the claims. Narrow, well-delineated claims reduce invalidation risks and facilitate targeted enforcement against infringers.

2. Can competitors develop similar compounds without infringing?
If they design around the specific structural features claimed or target different therapeutic indications, they may avoid infringement. However, detailed analysis against the claims is essential.

3. Does the patent cover formulations or just chemical compounds?
Most likely, it covers both compounds and formulations, with secondary claims addressing delivery systems or specific pharmaceutical compositions.

4. How does patent NO2019012 fit into the global patent landscape?
It possibly belongs to a wider patent family, with filings in the EU, US, or other jurisdictions, to secure comprehensive market protection and prevent bypasses.

5. What is the importance of patent landscape analysis for pharmaceutical innovation?
It helps identify white spaces, avoid infringement, and inform licensing strategies, ensuring sustainable commercial development.


References

  1. Norwegian Industrial Property Office (NIPO). Patent NO2019012 database entry.
  2. European Patent Office (EPO). Worldwide patent family data.
  3. WIPO PATENTSCOPE. Patent landscape reports relevant to pharmaceutical compounds.
  4. Patent law principles. “Claims construction and patent validity,” Harvard Law Review.

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