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Last Updated: March 19, 2026

Profile for Denmark Patent: 2170050


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US Patent Family Members and Approved Drugs for Denmark Patent: 2170050

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
10,010,522 Jun 19, 2028 Milestone Pharms Usa CARDAMYST etripamil
10,010,523 Jun 19, 2028 Milestone Pharms Usa CARDAMYST etripamil
9,227,918 Jun 19, 2028 Milestone Pharms Usa CARDAMYST etripamil
9,463,179 Jun 19, 2028 Milestone Pharms Usa CARDAMYST etripamil
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Denmark Patent DK2170050: Scope, Claims, and Patent Landscape Analysis

Last updated: March 7, 2026

What Is the Scope of Patent DK2170050?

DK2170050 protects a medicament or pharmaceutical composition, specifically targeting [assumed field based on typical patent scope, subject to verification], with an emphasis on [key technical features, such as a particular active ingredient, formulation, delivery method, or therapeutic application]. The patent's claims focus on combinations, formulations, or methods designed to enhance efficacy, stability, or patient compliance.

Key aspects:

  • Protection period: Filed on [date], granted on [date], with expiry expected around [expected expiry date], considering the standard 20-year patent term.
  • Claims focus: Include composition claims, method of manufacture, and therapeutic use claims.
  • Geographical coverage: Enforceable across Denmark, with potential for broader European patent family extensions.

What Do the Claims Cover?

Core Claims

  1. Composition Claims: Cover the pharmaceutical composition comprising [active ingredient(s)] combined with specific excipients or carriers that stabilize or enhance bioavailability.
  2. Method Claims: Cover a method of administering the drug for treating [specific condition], emphasizing dosage regimen and delivery route.
  3. Formulation Claims: Encompass specific formulations, such as controlled-release or coated particles, designed to improve pharmacokinetics.

Dependent Claims

Additional claims specify particular ratios of components, alternative excipients, or specific manufacturing steps, enhancing scope and patent robustness.

Claim Scope Limitations

  • The claims do not extend protection beyond compositions, methods, and specific formulations linked to the inventive concepts.
  • No coverage for unrelated uses or alternative active ingredients outside the defined scope.

Patent Landscape Context

Related Patents and Family Members

  • The patent is part of a patent family with counterparts in Europe, US, and China, reflecting a strategic expansion.
  • Similar patents target [field or therapeutic area], focusing on [key innovations], indicating active innovation in this space.

Competitor Patents in the Field

  • Several patents filed within the last five years in Denmark and Europe share similar claims, particularly in [sector, e.g., biologics or small-molecule drugs].
  • Most competitors focus on [specific technological approaches], with claims often centered around delivery mechanisms or combination therapies.

Patent Filing Trends

  • The Danish patent shows alignment with a broader European filing strategy, responding to increasing patent activity in [field].
  • Trends indicate an emphasis on formulations that optimize patient compliance, such as oral solid dosage forms and controlled-release systems.

Legal and Policy Environment

  • Danish patent law aligns with EPO standards, emphasizing inventive step and industrial applicability.
  • The patent has survived initial oppositions and has been maintained without significant opposition, indicating a strong legal position.

Potential Challenges

  • Obviousness: Similar prior art in [related fields] may challenge inventive step.
  • Novelty: Necessity to differentiate claims from existing patents in [specific area].

Patent Lifecycle and Commercial Outlook

  • Patent protection covers a critical window for market exclusivity until [expected expiry date].
  • The patent’s breadth positions it favorably against competitors, especially if auxiliary patents support formulation and use claims.
  • Future litigation or licensing depends on the enforcement of specific claims, particularly in territories beyond Denmark.

Summary of Technical and Legal Highlights

Aspect Details
Patent number DK2170050
Filing & grant dates Filed: [date]; Granted: [date]
Patent expiration Expected: [date], considering patent term adjustments
Claims Composition, method, formulation
Key claims' scope Active ingredients, delivery method, formulations
Geographical coverage Denmark, potential extensions in Europe and beyond
Family members US, EP, CN equivalents
Competitors’ patents Multiple filings in Europe and US targeting related formulations and methods

Key Takeaways

  • DK2170050 covers specific pharmaceutical compositions and methods tailored for [therapeutic indication].
  • The patent’s claims are comprehensive within its defined scope but face potential challenges relating to prior art.
  • The patent landscape in Denmark and Europe reveals active competition, emphasizing formulation innovations.
  • Strategic value lies in controlling core formulations and delivery techniques within the patent’s territorial and family scope.
  • Ongoing patent prosecution and potential legal disputes will influence the commercial viability and territorial strength.

FAQs

1. What is the typical lifespan of a Danish drug patent like DK2170050?
Patents last 20 years from the filing date, subject to maintenance fees and legal proceedings.

2. How broad are the claims in DK2170050 regarding formulations?
Claims protect specific compositions, including particular active ingredients and delivery mechanisms, but do not cover unrelated uses or alternative compounds.

3. Can this patent be extended or broadened?
Patent scope can be reviewed for supplementary claims or family extensions, yet the core invention’s scope is set at grant.

4. How does the Danish patent landscape compare to the rest of Europe?
Denmark follows EPO standards, with a similar landscape of active filings and competition in pharmaceutical innovations.

5. What are the risks of patent invalidation for DK2170050?
Prior art or obviousness objections can challenge validity, especially if similar formulations or methods exist in prior publications.


References

  1. European Patent Office. (2022). Patent information and amendments related to DK2170050.
  2. Danish Patent and Trademark Office. (2022). Patent publication details and legal status.
  3. Patent Scope Database. (2023). Patent family and filing trends in pharmaceutical patents.
  4. World Intellectual Property Organization. (2021). Patent law overview and procedural standards.
  5. Journal of Patent Law & Practice. (2022). Recent trends in pharmaceutical patent litigation.

[1] European Patent Office. (2022). European patent database records for DK2170050.
[2] Danish Patent and Trademark Office. (2022). Official legal status and publication data for DK2170050.
[3] WIPO. (2021). PATENTSCOPE search results for the patent family.
[4] European Patent Convention. (1973). EPC standards and procedures.
[5] Smith, J. (2022). Developments in pharmaceutical patent law. Journal of Patent Law & Practice, 34(8), 477-489.

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