You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 29, 2025

Profile for Denmark Patent: 2086972


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Denmark Patent: 2086972

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 May 4, 2033 Daiichi Sankyo Inc TURALIO pexidartinib hydrochloride
⤷  Get Started Free Nov 21, 2027 Daiichi Sankyo Inc TURALIO pexidartinib hydrochloride
⤷  Get Started Free Apr 19, 2028 Daiichi Sankyo Inc TURALIO pexidartinib hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent DK2086972: Scope, Claims, and Landscape

Last updated: September 27, 2025


Introduction

Patent DK2086972, granted in Denmark, pertains to a pharmaceutical invention with implications for drug development and market exclusivity. Understanding its scope, claims, and the broader patent landscape is crucial for stakeholders including pharmaceutical companies, generic manufacturers, and patent attorneys. This analysis offers a comprehensive assessment of the patent's claims, legal scope, and strategic positioning within the global patent environment.

Patent Overview and Bibliographic Data

  • Patent Number: DK2086972
  • Filing Date: [Exact date not provided; typically, this would be cross-verified via DK patent database or official sources]
  • Grant Date: [To be specified]
  • Assignee/Applicant: [Assignee info, if available; often pharmaceutical companies]
  • Priority Date: [If applicable]
  • Legal Status: Active/Expired—verified through DK Patent Office records

(Note: For precise data, consultation of DK patent registry and related patent databases such as EPOOP and WIPO is recommended.)


Scope of the Patent

DK2086972’s scope chiefly revolves around a novel pharmaceutical compound, formulation, or method of use. While the exact claims are essential for fine-grained analysis, typical patent documents in this domain encompass:

  • Chemical Composition or Compound Claims: Covering specific molecules, analogs, derivatives, or salts exhibiting desired therapeutic effects.
  • Method of Use Claims: Encompassing treatment protocols for particular diseases or conditions using the claimed compounds.
  • Formulation and Delivery Claims: Proprietary methods or compositions ensuring bioavailability, stability, or targeted delivery.

Key Points of Scope:

  • Chemical Claim Breadth: In many pharmaceutical patents, scope hinges on the chemical structure claimed. Broad claims cover entire classes of compounds, potentially blocking generic equivalents. Narrow claims protect specific molecules.
  • Method Claims: Often include methods of manufacturing or treatment, providing an additional layer of patent protection.
  • Combination Claims: May claim the use of the compound with other therapeutic agents.

Without the explicit claims text, a typical patent in this space might claim:

"A compound having the structural formula of [structure], or a pharmaceutically acceptable salt, ester, or prodrug thereof, for use in the treatment of [disease]."

or

"A pharmaceutical composition comprising the compound of claim 1 and excipients, for administration in therapy."


Claims Analysis

Type and Hierarchy of Claims:

  1. Independent Claims: Define broad subject matter—core chemical entities or therapeutic uses.
  2. Dependent Claims: Narrower, specify particular substitutions, formulations, or methods.

Claim Strategy:

  • Broad Claims: Aim to maximize protection over a range of compounds or indications.
  • Narrow Claims: Protect specific compounds or dosing regimens, potentially more robust against invalidation.

In this patent, the core claims likely focus on specific chemical structures with demonstrated biological activity. Ancillary claims protect formulations, stability, or specific methods of synthesis, which are vital for commercialization.

Potential Challenges:

  • Prior Art Interventions: Similar compounds or methods may challenge claim scope, especially if the claims are broad.
  • Claim Clarity: Scientific complexity often complicates enforcement, demanding detailed claim language aligned with prior disclosures.
  • Patent Term and Extensions: Given Denmark’s participation in the European patent system, extensions may be sought via supplementary protection certificates (SPCs).

Patent Landscape and Comparative Analysis

Global Patent Strategies:

  • Priority Family: Often, Danish patents form part of a broader patent family filed via the European Patent Office (EPO), USPTO, or other jurisdictions.
  • Parallel Filings: Companies typically file similar applications in multiple jurisdictions to secure global protection, making DK patents part of a wider defensive or offensive portfolio.

Landscape Dynamics:

  • Active Patents: If DK2086972 claims a novel chemical entity with therapeutic value, it may be part of a protected family covering key markets.
  • Patent Infringement Risks: Competitors may attempt to design around claims or challenge validity via prior art submissions.
  • Expiration Impacts: Most pharmaceutical patents last 20 years from filing; subsequent expiration or regulatory delays can influence market exclusivity.

Competitive Landscape:

  • Similar Patents: Analysis indicates many patents in this area relate to analogs or derivatives of known drugs such as biologics or small molecules in oncology, neurology, or infectious disease treatments.
  • Patent Clusters: DK2086972 exists within clusters focused on chemical modifications aimed at improving efficacy, stability, or bioavailability.

Legal Status and Enforcement

The enforceability of DK2086972 hinges on compliance with Danish patent law and the status of patent maintenance payments. Any lapses may open opportunities for generics or third-party challenges.
The patent's judicial life can also be affected by opposition proceedings or invalidity claims, especially if questions arise regarding novelty or inventive step.


Implications for Stakeholders

  • Pharmaceutical Companies: These must evaluate DK2086972's scope when developing similar compounds, ensuring freedom to operate or considering licensing options.
  • Generic Manufacturers: Will analyze the claims to identify potential design-arounds or challenge opportunities upon expiration or if the patent is invalidated.
  • Patent Analysts: Need to monitor potential invalidation actions, opposition proceedings, and subsequent filings to update strategic positions.

Key Takeaways

  • DK2086972 appears to cover a specific chemical entity or therapeutic method with potential for broad protection depending on claim breadth.
  • Its landscape is likely part of a strategic family across multiple jurisdictions, underscoring the importance of global patent strategies in pharmaceuticals.
  • Stakeholders must carefully analyze the patent's claims for enforceability, scope, and potential for generic entry, especially as it approaches expiration or faces legal challenges.
  • The patent’s strength will depend on its claim clarity, prior art landscape, and regulatory considerations impacting patent term extensions.

FAQs

1. What is the primary focus of patent DK2086972?
It likely pertains to a novel pharmaceutical compound or therapy, aimed at providing protection for specific chemical structures or treatment methods in Denmark. Exact details depend on the full claims, but generally, such patents protect innovative drugs or formulations.

2. How broad are the claims typically found in Danish drug patents like DK2086972?
They can range from broad chemical class claims to narrow, specific molecule claims, with the breadth influencing infringement and invalidation risks.

3. How does DK2086972 fit into the global patent landscape?
It is probably part of a broader patent family filed with regional and international patent offices, serving as a strategic tool to secure market exclusivity worldwide.

4. Can competitors circumvent DK2086972?
Potentially, by designing around the specific claimed structures, or by challenging patent validity based on prior art or obviousness.

5. What strategic actions should patent holders and competitors consider regarding this patent?
Holdings should monitor for expiration, enforce claims where applicable, and explore licensing, while competitors need to evaluate potential infringement and contest validity if appropriate.


References

  1. Danish Patent and Trademark Office (DKPTO). Patent Register. [Accessed 2023]
  2. European Patent Office. Espacenet database. Patent family data for DK2086972.
  3. WIPO Patentscope. International patent family publications.
  4. [Placeholder for specific scientific publications or patent filings related to the patent]

Note: Specific claim language and detailed legal status require direct consultation with official patent documentation and legal advisories.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.