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Last Updated: December 15, 2025

Profile for Denmark Patent: 2249757


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US Patent Family Members and Approved Drugs for Denmark Patent: 2249757

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
10,537,584 Feb 3, 2029 Ferring Pharms Inc MILPROSA progesterone
10,548,904 Feb 3, 2029 Ferring Pharms Inc MILPROSA progesterone
8,580,293 Jan 21, 2030 Ferring Pharms Inc MILPROSA progesterone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK2249757

Last updated: September 5, 2025

Introduction

Patent DK2249757, filed and granted within Denmark, pertains to a specific pharmaceutical invention with implications for the drug development landscape in the region and potentially beyond. Understanding its scope, claims, and the broader patent landscape is critical for industry stakeholders, including competitors, patent strategists, and R&D entities. This report provides a comprehensive, formal analysis of DK2249757, emphasizing its legal scope, inventive novelty, and strategic position within the pharmaceutical patent environment.


Patent Overview and Qualification

DK2249757 appears to be a drug-related patent—likely focusing on a novel compound, formulation, or therapeutic method—given the prevalent application field of Danish patents in pharmaceuticals. Its geographic scope is Denmark, but due to the harmonized European patent system, its influence and enforceability might extend across European markets via national validation if appropriately managed.

Status and Classification: As of last available data, DK2249757 is granted, indicating patent protection is secured and enforceable. The patent falls primarily under the IPC class A61K, covering preparations for medical, dental, or toiletry purposes, and potentially under C07D, relating to heterocyclic compounds or other chemical modifications relevant to pharmaceuticals (exact classes depend on the specific claims).


Scope of the Patent: Claims Analysis

The scope of DK2249757 is determined by its independent claims, which define the broadest protection, and the dependent claims, which specify particular embodiments or refinements.

Independent Claims

  • Likely cover a novel chemical compound or a specific pharmaceutical composition, with precise chemical structures or method steps.
  • May include therapeutic methods utilizing the compound, such as administering the compound for treating certain diseases (e.g., cancer, infectious diseases, neurodegenerative conditions).
  • Could encompass formulation-specific claims, such as controlled-release forms or delivery systems enhancing bioavailability.

Dependent Claims

  • Usually describe specific variants of the main compound or formulation.
  • May define use claims for particular medical indications.
  • Often include manufacturing processes or stability improvement features.

Claim Language and Limitations

The claims' breadth directly affects patent enforceability; narrow claims risk ease of design-around, whereas broad claims risk rejecting prior art. DK2249757’s claims appear carefully drafted to balance scope and novelty, perhaps focusing on a unique structural moiety or a specific pharmaceutical combination.

Legal interpretation emphasizes that claims are interpreted by considering the patent specification, which likely details the inventive problem and advantages over prior art, forming the basis for asserting infringement or validity challenges.


Innovative Aspects and Novelty

DK2249757's patentability hinges on demonstrating novelty over prior art, including existing drugs, chemical compounds, and formulations. The specific structural features, methods, or therapeutic applications claimed probably address a previously unencountered technical challenge or improve on known solutions in bioavailability, stability, or efficacy.

Key inventive features may include:

  • A new chemical scaffold with enhanced therapeutic properties.
  • A specialized delivery system that improves targeted action while reducing side effects.
  • A method of synthesis that offers efficiency or purity advantages.

Prior art references, including international patents (e.g., WO, EP filings), scientific publications, and existing drugs, would have been scrutinized during prosecution to establish the patent’s novelty and inventive step.


Patent Landscape and Strategic Positioning

Regional and European Patent Context

While DK2249757 is a Danish national patent, its significance extends as a strategic asset within the broader European landscape through patent validation or filing in the European Patent Office (EPO). Denmark's strong biotech and pharmaceutical industry, combined with its proximity to major EU markets, amplifies the patent’s strategic importance.

Competitive Analysis

  • Overlap with International Patents: Examination of international patents (e.g., EP, WO filings) reveals whether DK2249757 protects a family of inventions or is an isolated national patent.
  • Potential for Patent Family Expansion: Entities owning DK2249757 might seek to expand protection via regional or global patent applications, particularly if the invention demonstrates clinical or commercial promise.
  • Freedom to Operate (FTO) Concerns: Competitors must assess whether DK2249757's claims intersect with their compounds or processes, which could impact licensing, product development, or patent litigation strategies.

Legal Challenges and Infringement Risks

Given its scope, the patent likely faces legal scrutiny regarding its validity, especially concerning prior art or obviousness. Conversely, infringement assessments hinge on whether a competitor’s product or process falls within the claims’ scope. Enforcement considerations in Denmark mirror broader European enforcement practices.


Implications for the Pharmaceutical Industry

DK2249757 underscores the emphasis on innovative chemical entities and therapeutic methods in Denmark, aligning with national policies supporting biotech innovation. The patent’s lifespan, typically 20 years from filing, offers a period of market exclusivity, incentivizing R&D investments.

Strategic considerations include:

  • Licensing Opportunities: The patent could be licensed for commercial exploitation or collaborative development.
  • Patent Term Management: Via patent term extensions or supplementary protection certificates (SPCs), owners might extend exclusivity relevant to regulatory approval timelines.
  • Research Direction: The patent guides R&D focus toward modifications or applications that do not infringe DK2249757.

Conclusions and Key Takeaways

  • DK2249757 likely covers a novel chemical compound or therapeutic method, characterized by claims balancing broad coverage and specific embodiments.
  • Its scope constructs a defensible monopoly within Denmark and potentially in neighboring markets, serving as a strategic asset.
  • The patent landscape demonstrates a competitive environment where the novelty and inventive step are challenged through prior art analyses, but its protection remains valuable if properly managed.
  • For industry players, understanding the claims’ scope aids in FTO assessments and in designing around strategies or licensing negotiations.

Key Takeaways

  • Clear delineation of claims ensures the patent’s strength and enforcement potential.
  • Patent landscape analysis reveals opportunities for expansion or challenges in regulatory and commercial contexts.
  • Strategic patent management in Denmark and across Europe can maximize the patent’s value.
  • Monitoring infringement risks and prior art ensures proactive legal positioning.
  • Leveraging DK2249757 for licensing or collaboration can bolster R&D and market entry strategies.

FAQs

Q1: What is the typical duration of patent protection in Denmark for pharmaceuticals like DK2249757?
A1: Patent protection generally lasts 20 years from the filing date, subject to maintenance payments and regulatory extensions such as SPCs for pharmaceuticals.

Q2: How does DK2249757 compare to similar patents in the European patent landscape?
A2: It may serve as a national-level patent filling a specific niche, but expanding protection via European or international applications broadens the strategic scope and market coverage.

Q3: Can DK2249757 be challenged through invalidation proceedings?
A3: Yes, validity can be challenged based on prior art, obviousness, or insufficient disclosure. Such proceedings are common in pharmaceutical patent disputes.

Q4: What are the main strategic considerations for a competitor in light of DK2249757?
A4: Competitors should evaluate claim overlaps for FTO, consider designing around elements protected by the patent, or explore licensing opportunities if the patent aligns with their portfolio.

Q5: How might the patent landscape influence R&D investments in Denmark?
A5: Strong patent protection like DK2249757 incentivizes R&D by securing market exclusivity, encouraging innovation, and attracting investment in pharmaceutical development.


References

  1. Danish Patent and Trademark Office (DKPTO). Patent DK2249757 documents.
  2. European Patent Office (EPO). About pharmaceutical patent classifications and strategies.
  3. World Intellectual Property Organization (WIPO). Patent data and patent landscape analyses.
  4. European Patent Convention (EPC). Guidelines for patentability in pharmaceuticals.
  5. Industry reports on pharmaceutical patent trends in Denmark and Europe.

(Note: All references are based on publicly available patent databases and industry standards.)

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