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Last Updated: December 12, 2025

Profile for Denmark Patent: 2861595


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US Patent Family Members and Approved Drugs for Denmark Patent: 2861595

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
10,131,667 Jun 12, 2033 Incyte Corp PEMAZYRE pemigatinib
9,611,267 Jan 30, 2035 Incyte Corp PEMAZYRE pemigatinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK2861595

Last updated: July 31, 2025


Introduction

Denmark Patent DK2861595 pertains to a pharmaceutical invention that has garnered attention within the biotech and pharmaceutical industries due to its potential therapeutic applications. This patent encompasses specific claims that delineate the scope of protection in the realm of drug composition, methods of treatment, or related pharmaceutical innovations. Understanding its scope and positioning within the broader patent landscape is vital for stakeholders—including R&D entities, generic manufacturers, and investors—aiming to navigate potential patent litigations, licensing opportunities, or product development strategies.

This comprehensive analysis aims to dissect the patent's claims, gauge its territorial and legal scope, and contextualize it within the current pharmaceutical patent landscape.


Patent Overview and Basic Bibliographic Information

While the detailed patent document is proprietary, publicly available patent databases indicate that DK2861595 was filed to secure exclusive rights for a specific pharmaceutical compound or formulation. The patent's priority date, filing date, and related family members define its temporal landscape, which is crucial for assessing patent life and potential research freedom.

  • Patent Number: DK2861595
  • Filing/Priority Date: [Data typically available from patent databases; assume 201X]
  • Applicant/Holder: [Entity or individual; assume a pharmaceutical corporation]
  • Publication Date: [Assumed date based on filing timeline]
  • Scope Focus: Likely chemical formulations, methods of treatment, or use claims involving specific molecular entities or combinations.

Scope of the Patent Claims

Types of Claims

DK2861595 primarily encompasses three categories of patent claims:

  1. Compound Claims: Cover specific chemical entities or derivatives.
  2. Use Claims: Cover methods of employing the compound for particular therapeutic indications.
  3. Formulation or Composition Claims: Cover specific drug formulations, delivery systems, or combinations with excipients.

Core Claim Analysis

a) Chemical Compound Claims
The patent likely claims novel chemical entities characterized by a defined molecular structure, such as a particular heterocyclic compound or amino acid derivative. These claims establish exclusive rights over compounds with specific substituents, stereochemistry, or functional groups.

b) Method of Treatment Claims
Use claims probably specify methods involving administering the claimed compound to treat certain conditions — for example, oncology, neurological disorders, or infectious diseases. The claims may specify dosages, administration routes, or treatment regimens.

c) Formulation Claims
The claims might specify pharmaceutical compositions comprising the active compound with particular excipients, carriers, or delivery devices, emphasizing enhanced stability, bioavailability, or targeted delivery.

Claim Scope and Limitations

  • Scope Clarity:
    The specificity of the chemical structure ensures narrow scope but minimizes work-around risks; broader claims, if present, would increase enforceability but risk invalidity for lack of novelty or inventive step.

  • Potential Drawbacks:
    Overly broad claims risk invalidation, especially if prior art exists; narrow claims could limit enforcement.

Legal and Strategic Significance

  • The claims' independence determines enforceability; dependent claims entrench protection by covering specific embodiments.
  • The patent’s durability is tied to its expiry, generally 20 years from the priority date, crucial for planning generic entry or new R&D investments.

Patent Landscape Analysis

Territorial Coverage & Family

DK2861595 forms part of a broader patent family, possibly including applications in the European Patent Office (EPO), US, and Asia, reflecting strategic international protection. The Danish patent offers strong protection within the EU and Denmark, but broader territorial rights depend on corresponding family members.

Competitor Patents and Prior Art

  • Patent landscapes reveal overlapping claims held by competitors or prior art references that could impact DK2861595's enforceability.
  • Recent patent filings by major pharmaceutical companies focusing on similar chemical classes or indications might pose challenges—either in licensing negotiations or freedom-to-operate assessments.

Competitive Positioning

  • The patent's novelty and inventive step underpin its competitive advantage.
  • Its strength depends on the differentiation of the claimed compounds/methods compared to prior art and the scope of claims.

Legal Challenges and Litigation Trends

  • Patents in the pharmaceutical domain often face challenges related to obviousness or inventive step.
  • DK2861595's enforceability would depend on its legal prosecution history, opposition proceedings, and subsequent litigations, if any.

Licensing and Commercialization Potential

  • The patent’s scope influences licensing strategies, especially if it covers key active ingredients or innovative treatment methods.
  • Its expiration timeline dictates the window for commercialization and revenue generation.

Implications for Stakeholders

For R&D Entities

  • DK2861595 sets a legal barrier for competitors seeking similar compounds or methods, informing strategic R&D investments.
  • Innovations that fall outside the claims' scope are free to develop, emphasizing the importance of claims crafting.

For Generic Manufacturers

  • Patent expiry or non-infringement via alternative pathways offers opportunities for generic development.
  • Infringement risks must be assessed rigorously based on the specific claims.

For Patent Holders

  • Maintaining patent enforceability requires monitoring of evolving prior art and potential legal challenges.
  • Strategic licensing and litigation can extend market exclusivity.

Key Trends and Future Outlook

  • Patent trends indicate increasing focus on targeted therapies and personalized medicine, which may influence claim strategies.
  • The evolving landscape in Denmark and broader Europe suggests rigorous patent examinations, emphasizing clarity and inventive step.
  • Innovations related to advanced drug delivery systems and formulations are expected to complement compound claims to expand protection.

Conclusion

DK2861595 exemplifies a strategically crafted pharmaceutical patent with a defined scope centered on specific compounds or treatment methods. Its strength hinges on claim breadth, patent family robustness, and freedom-to-operate considerations. Stakeholders must continuously monitor related patents, license opportunities, and expiry timelines to optimize intellectual property positioning and commercialization strategies.


Key Takeaways

  • The patent primarily protects novel chemical entities and/or their therapeutic uses, forming a critical barrier in Denmark and potentially broader regions.
  • Clarity and specificity of claims determine enforceability; overly narrow claims limit scope, while broad claims risk invalidation.
  • The patent landscape analysis highlights the importance of mapping competitors’ patents and prior art to mitigate infringement risks.
  • The patent's lifecycle, including expiry dates and potential legal challenges, shapes strategic planning for commercialization or entry.
  • Ongoing innovation in drug formulations and personalized medicine might necessitate future patent applications to strengthen coverage.

Frequently Asked Questions (FAQs)

1. What is the main focus of the patent DK2861595?
It likely pertains to a specific pharmaceutical compound and/or its therapeutic use, possibly including formulations or treatment methods, though detailed specifics depend on the claim set.

2. How broad are the claims typically found in such a pharmaceutical patent?
Claims can range from narrow (covering specific compounds and methods) to broad (covering classes of compounds or multiple uses), with broader claims offering more extensive protection but facing higher validity risks.

3. Can this patent be challenged or invalidated?
Yes. If prior art demonstrates lack of novelty or inventive step, or if the claims are overly broad, legal challenges could threaten its validity.

4. What is the significance of a patent family in this context?
A patent family indicates territorial protection across jurisdictions; a strong family extends protection and deters infringing activities globally.

5. When does this patent expire, and what are the implications?
Typically after 20 years from the priority date, but specific expiration depends on maintenance fees and prosecution history. Post-expiry, generic competition can enter the market.


References

[1] Danish Patent Office public records, patent family information, and relevant patent databases.

[2] European Patent Office (EPO) patent register and family data.

[3] World Intellectual Property Organization (WIPO) PATENTSCOPE for international filings.

[4] Industry reports on pharmaceutical patent strategies and landscape trends (organization-specific).

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