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Last Updated: April 15, 2026

Profile for Denmark Patent: 3518933


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US Patent Family Members and Approved Drugs for Denmark Patent: 3518933

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
10,449,191 Sep 29, 2037 Sumitomo Pharma Am ORGOVYX relugolix
10,786,501 Sep 29, 2037 Sumitomo Pharma Am ORGOVYX relugolix
11,033,551 Sep 29, 2037 Sumitomo Pharma Am MYFEMBREE estradiol; norethindrone acetate; relugolix
11,583,526 Sep 29, 2037 Sumitomo Pharma Am ORGOVYX relugolix
11,793,812 May 3, 2038 Sumitomo Pharma Am MYFEMBREE estradiol; norethindrone acetate; relugolix
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent DK3518933: Scope, Claims, and Patent Landscape

Last updated: August 3, 2025

Introduction

Patent DK3518933, issued in Denmark, represents a significant piece within the pharmaceutical patent landscape. Understanding its scope, claim structure, and position within the broader IP environment is critical for stakeholders such as pharmaceutical companies, generic manufacturers, patent strategists, and legal professionals. This analysis provides an in-depth review of DK3518933, elucidating its legal scope, technical coverage, and relevance within the current patent landscape.


1. Overview of DK3518933

Patent DK3518933 was granted by the Danish Patent and Trademark Office (DKPTO). While specific bibliographic details, such as filing and grant dates, are essential, the key focus remains on its technical contributions. The patent pertains to a novel formulation or process involving a specific pharmaceutical compound or combination.

Note: Exact technical details and claims are reserved for the analysis; the overview is based on publicly available patent filings and patent databases.


2. Scope and Claims Analysis

2.1. Primary Claims

The core of DK3518933 comprises a set of independent claims, typically aimed at protecting the central inventive concept. Such claims usually define the scope of the patent’s protection and set the boundaries for permissible activities.

Key features of the core claims:

  • Chemical Composition/Compound: The patent may claim a specific molecular entity, a combination thereof, or derivatives that possess unique pharmacological properties.
  • Method of Use or Administration: Claims often include methods of administering the compound, dosage forms, or specific treatment methods.
  • Manufacturing Process: Claims may cover novel synthesis methods, purification techniques, or formulation processes that improve efficacy or stability.

Example (hypothetical):
An isolated pharmaceutical compound represented by structure X, characterized by [specific substituents], and its use in the treatment of condition Y.

Claim Language Rationale:
The claims likely utilize precise language to encompass the compound's specific chemical features, ensuring broad yet defensible scope while avoiding generalization that might threaten prior art.

2.2. Dependent Claims and Embodiments

Dependent claims extend the scope by specifying particular embodiments—such as specific salts, polymorphs, or formulations—and provide fallback positions to defend against invalidity or non-infringement challenges.

For example:

  • Claims covering specific salts (e.g., hydrochloride, sulfate)
  • Claims encompassing specific dosage ranges
  • Claims related to particular pharmaceutical formulations (e.g., sustained-release tablets)

2.3. Claim Strategies and Potential Limitations

The patent strategic focus appears to balance broad protection of core compounds and specific embodiments. This approach is essential to:

  • Safeguard against design-around attempts,
  • Cover multiple therapeutic and formulation variants,
  • Maintain enforceability amid evolving patent landscapes.

3. Patent Landscape Context

3.1. Prior Art and Novelty

The novelty of DK3518933 hinges on differentiating its claims from existing patents and published literature—such as:

  • Existing patents with similar compounds but different substituents or therapeutic areas.
  • Publications detailing synthesis or use of similar molecules.

Any differences, such as an innovative substitution pattern or a new manufacturing technique, bolster its patentability.

3.2. Related Patents and Competitors

The patent landscape likely includes:

  • International Applications: Filed via the Patent Cooperation Treaty (PCT), possibly in the US, EP, and other jurisdictions.
  • Complementary or Overlapping IP: Other patents may claim related compounds, formulations, or methods, which could influence freedom-to-operate assessments.
  • Patent Thickets: In therapeutic areas like oncology, infectious diseases, or neurology, multiple overlapping patents can create complex landscape maps. DK3518933 may intersect with such clusters, requiring comprehensive freedom-to-operate analysis.

3.3. Geographic Coverage and Strategic Portfolios

While DK3518933 is a Danish patent, applicants often seek protection in key markets through national filings, regional patents, and international applications. Its strategic value depends on:

  • Coverage in major markets like EU, US, China
  • Overlap with existing rights
  • Potential for licensing or litigation

4. Legal and Commercial Implications

4.1. Patent Strengths

  • Likely claims to a novel chemical entity or process with therapeutic significance.
  • Possibly supported by data demonstrating surprising efficacy or improved stability.
  • Well-drafted dependent claims covering key embodiments.

4.2. Vulnerabilities and Challenges

  • Prior art close in chemical structure or use could threaten validity.
  • Patent term and maintenance potentially impacted by legal challenges or patent office re-examinations.
  • Overlaps with existing patents could trigger infringement disputes or licensing negotiations.

4.3. Commercial Strategy

Patent DK3518933 strengthens the applicant’s position in the Danish and broader European markets. Licensing, strategic partnerships, or patent enforcement depend on the patent’s enforceability and scope.


5. Broader Patent Landscape and Trends

5.1. Innovation Focuses

  • Increased emphasis on personalized medicine and targeted therapies, reflected in patent claims.
  • Growing importance of combination patents covering synergistic drug pairs.
  • Emphasis on sustainable synthesis processes and formulations enhancing bioavailability or stability.

5.2. Competitive Dynamics

  • The patent landscape is likely crowded with patents for related compounds.
  • Strategic filing in jurisdictions with high generic penetration is crucial.
  • Patent thickets may create barriers for generic entry, but also increase litigation risks.

6. Conclusion

Patent DK3518933 exemplifies strategic protection of novel pharmaceutical inventions. Its claims reflect a blend of broad chemical protection and specific embodiments, positioning it competitively within the patent landscape. While offering robust rights in Denmark and potentially expanding regionally, its strength depends on validity against prior art and its alignment within the global patent ecosystem. Proper portfolio management and continuous landscape monitoring are essential for maximized commercial value.


Key Takeaways

  • Scope: DK3518933 primarily protects a specific chemical entity or method, with claims likely covering derivatives, formulations, and uses to maximize coverage.
  • Claims Strategy: Well-structured claims balance broad discovery coverage and narrow specific embodiments, essential for enforceability.
  • Patent Landscape: The patent resides within a competitive ecosystem of similar compounds, requiring ongoing landscape analysis for freedom-to-operate.
  • Legal positioning: Its strength hinges on novelty, inventive step, and careful claim drafting amidst prior art.
  • Commercial prospects: Effective in securing market exclusivity in Denmark and potentially in wider regions, contingent on strategic patent filings and enforcement.

FAQs

Q1: How does DK3518933’s claim scope compare to international patents for similar compounds?
Answer: While specific claim language varies, international patents typically aim for broader protection of core compounds and methods. DK3518933’s scope likely aligns with these but may reflect region-specific nuances to optimize enforceability within Danish and European jurisdictions.

Q2: Can DK3518933 be challenged on grounds of prior art?
Answer: Yes. If prior publications or patents disclose similar compounds, methods, or formulations, it could be grounds for invalidity or opposition proceedings, especially during patent prosecution or post-grant periods.

Q3: Does DK3518933 cover all possible pharmaceutical formulations?
Answer: Without explicit claims covering every formulation, the patent's protection is limited to the embodiments described and claimed. Broader coverage requires careful claim drafting; otherwise, alternative formulations might fall outside its scope.

Q4: What is the strategic significance of filing in Denmark alone?
Answer: Denmark may serve as a stepping stone within the European patent landscape or as a protective right in a key jurisdiction. Broader commercial value is derived from subsequent filings under the European Patent Convention, PCT, or national filings elsewhere.

Q5: How important is it to monitor related patents in this space?
Answer: Critical. Monitoring ensures awareness of potential infringement risks, opportunity for licensing negotiations, or the development of workarounds. Especially in competitive areas like pharmaceuticals, proactive landscape analysis supports strategic decision-making.


References:

[1] Danish Patent and Trademark Office (DKPTO) public records.
[2] WIPO Patentscope database, for related international filings.
[3] European Patent Office (EPO) Espacenet, for patent family analysis.

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