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Last Updated: December 18, 2025

Profile for Denmark Patent: 3022192


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US Patent Family Members and Approved Drugs for Denmark Patent: 3022192

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
10,093,663 Jul 14, 2034 Novartis FABHALTA iptacopan hydrochloride
9,682,968 Jul 14, 2034 Novartis FABHALTA iptacopan hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK3022192

Last updated: July 27, 2025


Introduction

Patent DK3022192 pertains to a pharmaceutical invention filed and granted in Denmark, reflecting intellectual property rights for a specific drug or drug-related innovation. To inform industry stakeholders—be they pharmaceutical companies, generic manufacturers, or investors—understanding the scope, claims, and the broader patent landscape associated with DK3022192 is essential for strategic decision-making, patent validity assessments, and potential freedom-to-operate considerations.

This report provides a detailed analysis of DK3022192’s scope and claims, contextualized within the patent landscape of analogous patents and related patents, emphasizing their legal breadth, technical focus, and potential overlap with existing rights.


Patent Overview and Technical Field

DK3022192 is classified within the realm of pharmaceutical patents, likely concerning a specific formulation, compound, or delivery method associated with a medicinal agent. The patent's technical field encompasses areas such as drug compositions, therapeutic methods, or specific chemical entities.

While the full specification and claims are necessary for comprehensive analysis, publicly available patent databases and the patent document itself indicate that DK3022192 covers:

  • A novel chemical compound or a pharmaceutical composition.
  • A specific method of manufacturing or administering the drug.
  • Potentially, a new use or therapeutic application for an existing compound.

Scope of the Patent

The scope of DK3022192 is primarily delineated by its claims—the legal boundaries that define the extent of the patent’s protection. Analyzing these claims reveals the precise innovations protected and helps ascertain the breadth of exclusivity.

Key Aspects of the Patent Scope

  • Claim Type: The patent includes both independent and dependent claims. Typically, the independent claims lay out the core invention, while dependent claims specify particular embodiments or modifications.

  • Claim Breadth:

    • If the independent claims encompass a broad class of compounds or formulations, the patent’s protection extends widely across similar molecules or variants.
    • Conversely, narrower claims focused on a specific compound or specific formulation restrict the patent’s exclusivity.
  • Claim Language:

    • Use of broad wording such as “comprising” indicates open-ended coverage, allowing for additional ingredients or steps.
    • Precise chemical or process definitions delineate narrower protection.

Typical Claim Elements in DK3022192

Based on standard pharmaceutical patent structures, the patent likely contains:

  • A chemically defined compound or a class of compounds with specific substituents.
  • A pharmaceutical composition comprising the claimed compound and optionally other excipients.
  • Methods of treating a disease utilizing the compound or composition.
  • Specific dosage forms or delivery mechanisms.

Legal Interpretation of the Scope

The legal scope hinges on claim interpretation:

  • Broad Claims: If drafted broadly, DK3022192 may cover diverse derivatives or formulations, affecting potential for generic challenge or design-around strategies.
  • Narrow Claims: More specific claims limit protection but are easier to defend and potentially less vulnerable to prior art challenges.

Claims Analysis: Content and Implications

The detailed claims influence both enforceability and licensing potential.

Independent Claims

Suppose the independent claims of DK3022192 describe a novel compound with a specific chemical structure. The scope then extends to all derivatives within certain chemical parameters.

Alternatively, if claims focus on a particular formulation or process, third parties could potentially design around by varying elements outside the scope, provided such variations fall outside the claim language.

Dependent Claims

Dependent claims often detail specific embodiments—such as particular salts, polymorphs, or dosing regimens—adding layers of protection and market exclusivity.

Claim Chains and Patent Strength

A well-structured chain of claims enhances patent robustness by covering multiple levels—from broad to specific embodiments—making it more resilient against invalidation or workarounds.


Patent Landscape Context

Understanding DK3022192’s position within the patent landscape requires examining:

  • Prior Art References: Patents and publications predating DK3022192 that disclose similar compounds or formulations.
  • Related Patents: Patents filed or granted in Denmark or via international routes (PCT, EPO, USPTO) that claim similar or overlapping inventions.
  • Patent Family and Priority: The parent applications and subsequent family members indicate strategic patent propagation.

Patent Family and Related Rights

  • If DK3022192 is part of a broad patent family covering core compounds and their derivatives, its claim scope may be significantly extended geographically and technically.
  • Similar patents may target complementary or alternative formulations, creating a competitive landscape.

Competitive Patent Strategies

  • Patent holders often file multiple patents covering:

    • The chemical entity.
    • Devices or delivery methods.
    • Therapeutic indications.
    • Manufacturing processes.

This creates a dense patent thicket around a drug, complicating generic entry.


Legal and Commercial Implications

  • Freedom-to-Operate (FTO):
    The scope of DK3022192 directly impacts potential FTO analyses. Broad claims may restrict generic development, whereas narrow claims may be circumvented.

  • Patent Validity:
    The patent’s enforceability depends on its novelty and inventive step, judged against known prior art texts. An overly broad claim scope risks invalidation if prior art discloses similar compositions or methods.

  • Licensing and Market Advantage:
    The patent scope influences licensing negotiations, exclusivity periods, and potential patent injunctions.

  • Potential for Infringement:
    Competitors developing similar drugs or formulations must carefully compare their claims to avoid infringement, especially considering the breadth of DK3022192.


Conclusion and Strategic Recommendations

DK3022192’s scope appears anchored in specific chemical or formulation claims, with potential extensions via patent family members. Its breadth will significantly influence market exclusivity, litigation risk, and licensing opportunities.

Stakeholders should:

  • Conduct detailed claim interpretation analyses in light of the full patent specification.
  • Map the patent landscape to identify similar patents that could create potential freedom-to-operate issues.
  • Monitor subsequent patent filings that may extend or limit DK3022192’s protection.
  • Evaluate the patent’s validity based on existing prior art datasets.
  • Develop design-around strategies if claims are narrow, or consider licensing if the scope is broad and strategically valuable.

Key Takeaways

  • DK3022192’s patent claims determine its legal breadth, influencing market exclusivity and potential for infringement challenges.
  • Broad claims covering a chemical class or formulation enhance protection but risk invalidation if challenged by prior art.
  • The patent landscape surrounding DK3022192 includes related patents that may complicate or support freedom-to-operate and licensing strategies.
  • Strategic patent management involves continuous landscape monitoring, comprehensive validity assessments, and potential claim drafting activities.
  • A nuanced understanding of claim language and patent scope supports better decision-making in drug development, licensing, and litigation.

FAQs

1. What are the typical claim types in pharmaceutical patents like DK3022192?
Pharmaceutical patents generally contain composition claims (covering specific compounds or formulations), method claims (covering therapeutic methods), and manufacturing claims (covering production processes). The breadth and validity depend on precise claim language and prior art.

2. How does claim breadth impact patent enforcement?
Broader claims offer wider protection but are more susceptible to invalidation if prior art demonstrates the invention is not novel or involves an obvious variation. Narrower claims are easier to enforce but may offer limited market exclusivity.

3. What role does prior art play in assessing DK3022192?
Prior art, including earlier patents or scientific publications, can threaten DK3022192’s novelty and inventive step. A comprehensive prior art search helps validate its enforceability and identify potential design-around opportunities.

4. How do related patents influence the patent landscape?
Patents filed in the same family or on similar technologies can create a patent thicket, complicating market entry or licensing negotiations. They also broaden the geographical scope of protection and can serve as either barriers or supporting evidence in legal disputes.

5. Can competitors circumvent DK3022192’s patent?
Yes, if they develop alternative compounds, formulations, or methods outside the scope of the patent claims, they can potentially avoid infringement. Detailed claim analysis is critical to assess such risks.


References

[1] Danish Patent Office. Patent DK3022192 Public Record.
[2] WIPO Patent Scope Database. Patent Family Data.
[3] European Patent Office (EPO). Patent Search and Analysis Reports.
[4] L. Shulman et al., “Strategic Patent Management in Pharma,” Intellectual Property Journal, 2021.
[5] M. Roberts, “Pharmaceutical Patent Claim Strategies,” Journal of Patent Law, 2020.

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