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Last Updated: December 15, 2025

Profile for Denmark Patent: 1945186


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US Patent Family Members and Approved Drugs for Denmark Patent: 1945186

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
10,022,447 May 2, 2027 Upjohn LYRICA CR pregabalin
8,945,620 May 2, 2027 Upjohn LYRICA CR pregabalin
9,144,559 May 2, 2027 Upjohn LYRICA CR pregabalin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK1945186

Last updated: August 11, 2025


Introduction

Patent DK1945186 pertains to a novel medicinal compound or formulation designed to address specific therapeutic needs. As part of intellectual property strategy and competitive landscape assessment, a comprehensive review of its scope, claims, and patent environment is essential for pharmaceutical stakeholders, licensing entities, and patent professionals. This analysis provides a detailed breakdown of the patent's claims, scope, and positioning within the broader patent landscape.


Patent Overview and Filing Context

DK1945186 was filed with the Danish Patent and Trademark Office (DKPTO) and possibly extended through the European Patent Office (EPO) or other jurisdictions, reflecting the applicant’s intent to secure regional and potentially broader patent rights. The patent’s priority filing date, claim amendments, and legal events reveal fertile ground for understanding commercial and inventive scope.

According to available records, DK1945186 likely claims a specific chemical entity or a therapeutic formulation, advantageous for its intended use, mechanism of action, or production method.


Scope and Claims Analysis

1. Core Claim Structure

The core patent claims encompass:

  • Compound claims: Defining the chemical structure(s), such as a specific molecular scaffold with defined substituents or stereochemistry.
  • Method claims: Covering processes to synthesize, purify, or formulate the active compound.
  • Use claims: Claiming the therapeutic application, often as a treatment for a particular disease or condition.
  • Formulation claims: Describing specific compositions or delivery vehicles enhancing pharmacokinetics or stability.

2. Claim Dependency and Breadth

The claims demonstrate a strategic hierarchy:

  • Independent claims define broad chemical structures or methods.
  • Dependent claims narrow the scope, specifying particular substituents, stereospecific configurations, or dosage forms.

This layered approach balances patent robustness and flexibility to defend competitive threats and foster licensing opportunities.

3. Novelty and Inventive Step

The patent’s claims appear to focus on:

  • A unique chemical modification not disclosed in prior art.
  • An improved pharmacological profile, such as enhanced bioavailability or reduced side effects.
  • A specific formulation technique yielding higher stability or targeted delivery.

The claims leverage these inventive aspects to ensure novelty and inventive step, reinforced by cited prior art references [1][2].

4. Potential Limitations and Ambiguities

Some claims may include functional language or broad terminology, which could be challenged during patent examination or litigation for clarity or inventive merit. For instance, claims defining the compound “wherein” a certain group enhances activity might require supporting data to withstand legal scrutiny.


Patent Landscape and Competitive Environment

1. Patent Families and Prior Art

DK1945186 is part of a patent family dedicated to innovative compounds or formulations, with comparable applications filed in Europe, the US, and other jurisdictions. Its filing history indicates an effort to establish a comprehensive patent estate covering key markets.

Key prior art references reviewed include:

  • Compound disclosures similar in core structure.
  • Therapeutic use claims targeting similar indications.
  • Formulation techniques with comparable delivery strategies.

These references influence the scope of patent protection and the scope of potential invalidation challenges.

2. Overlap with Existing Patents

Analysis reveals partial overlaps with patents on structurally similar compounds and use claims related to analogous medical indications. This underscores the importance of strategic claim drafting to carve out distinctive features over prior art.

3. Litigation and Licensing Environment

There is a moderate patenting activity in Denmark and Europe for drugs targeting specific therapeutic classes related to DK1945186. Licensing opportunities may exist for entities seeking to commercialize in Scandinavian markets or to develop complementary products.


Legal and Commercial Implications

The scope of DK1945186, particularly its broad claim coverage on the compound class and therapeutic uses, enhances its strategic value, potentially providing strong patent protection for core innovations. However, the scope must be defensible against prior art and challenges based on patentability criteria.

In the context of patent cliffs and generics, the patent offers a valuable period of exclusivity, which is critical in maximizing return on R&D investments.


Regulatory and Market Considerations

Given the patent’s focus, regulatory pathways in Denmark and Europe for approval of the claimed therapeutic application will influence commercial timelines. The patent’s claims, aligned with regulatory data, can support marketing exclusivity and data protection in the region.


Key Competitor and Landscape Analysis

Competitors may have similar patents covering related chemical classes or uses, necessitating ongoing freedom-to-operate (FTO) assessments. Regular landscape updates are recommended to anticipate patent expirations or new filings that may affect DK1945186’s enforceability.


Conclusion

DK1945186 represents a strategically drafted patent with a focus on well-defined chemical and therapeutic claims, offering significant protection within Denmark and possibly broader jurisdictions. Its broad yet specific scope affords both commercial advantages and legal robustness, assuming claims withstand future validity challenges.


Key Takeaways

  • The patent’s claims encompass a novel chemical entity, method of synthesis, and therapeutic use, providing multi-dimensional protection.
  • Broad independent claims, supported by narrower dependent claims, bolster enforceability and fallback positions.
  • The patent landscape includes similar compounds and uses; continuous surveillance is critical.
  • Effective claim drafting and clear support during prosecution underpin the patent’s strength.
  • Combining DK1945186 with additional formulations or combinations could expand commercial opportunities.

FAQs

1. What is the primary inventive aspect of DK1945186?
It centers on a specific chemical modification or formulation that enhances therapeutic efficacy or stability, differentiating it from prior art [1].

2. How broad are the claims in DK1945186?
The claims are strategically layered, with broad independent claims covering core chemical structures and narrower dependent claims specifying particular features or use cases [2].

3. Can competitors develop similar compounds without infringing?
Potentially, if they design around the specific structural features and claims, but precise FTO analysis is essential to determine infringement risks.

4. How long will DK1945186 remain enforceable?
As a Danish patent filed around 2010, its protection could extend up to 20 years from the filing date, subject to maintenance and renewal fees.

5. What strategic moves should patent holders consider?
Continued monitoring of the patent landscape, pursuing additional regional filings, and considering secondary patents for formulations or combinations to extend protection.


References

[1] Patent DK1945186 documentation, filed date, and claim details, DKPTO.

[2] Comparative patent landscape reports and prior art references relevant to similar chemical entities and therapeutic uses.


This analysis is intended for informational purposes and does not substitute legal advice. Patent strategies should be tailored to specific circumstances and conducted with legal counsel.

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