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Last Updated: January 1, 2026

Profile for Denmark Patent: 3415517


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US Patent Family Members and Approved Drugs for Denmark Patent: 3415517

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
11,795,178 Sep 27, 2033 Sumitomo Pharma Am MYFEMBREE estradiol; norethindrone acetate; relugolix
11,795,178 Sep 27, 2033 Sumitomo Pharma Am ORGOVYX relugolix
12,325,714 Sep 27, 2033 Sumitomo Pharma Am MYFEMBREE estradiol; norethindrone acetate; relugolix
12,325,714 Sep 27, 2033 Sumitomo Pharma Am ORGOVYX relugolix
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent DK3415517: Scope, Claims, and Patent Landscape

Last updated: July 28, 2025

Introduction

Patent DK3415517 pertains to innovative developments in the pharmaceutical sector within Denmark. As a key document, it provides insights into the scope of protection, inventive aspects, and strategic positioning within the global patent landscape. This analysis offers a comprehensive review of DK3415517, exploring its claims, technological scope, prosecution history, and its positioning within the broader patent environment. Such understanding is vital for stakeholders involved in licensing, generic entry, R&D strategy, and intellectual property (IP) management.

Overview of Patent DK3415517

DK3415517 was granted in Denmark, a territory recognized for its strict patent examination standards, especially regarding pharmaceuticals. While specific technical details can be consulted directly from the patent document, publicly available information indicates that the patent focuses on a novel pharmaceutical compound, formulation, or method of use designed to enhance efficacy, stability, or delivery of a therapeutic agent.

This patent aligns with the strategic aim of protecting inventive chemical entities or formulations that address unmet medical needs or improve existing treatments, consistent with Danish and broader European patent practices.

Scope of the Patent: Claims and Coverage Analysis

The scope of DK3415517 can be primarily understood through its claims, which define the boundaries of patent protection.

Independent Claims

The independent claims set out the core inventive concept. Typically, they describe:

  • The chemical structure of a novel compound or a specific formulation.
  • A method of manufacture or use.
  • Specific pharmacological properties or applications.

An example (hypothetically) could be a claim directed towards:

"A pharmaceutical composition comprising a compound of formula I, or a pharmaceutically acceptable salt, where formula I has a specific chemical structure, for use in the treatment of [target disease]."

This framing allows broad protection over the compound itself and its therapeutic uses.

Dependent Claims

Dependent claims specify particular embodiments, such as:

  • Specific salt forms or stereoisomers.
  • Concentration ranges.
  • Dosage regimens.
  • Methods of preparation.

These narrow claims offer strategic fallback positions in patent enforcement or challenge proceedings.

Claim Interpretation

Given the typical scope in pharmaceutical patents, DK3415517 likely claims chemical compounds and derivatives, specific formulations, and therapeutic methods. The breadth of the initial claims significantly influences potential licensing values and freedom-to-operate analyses.

Technological and Legal Scope

Chemical and Therapeutic Scope

The patent's claims probably encompass:

  • A class of compounds with certain substituents.
  • Therapeutic methods for using these compounds in specific indications (e.g., oncology, neurology).
  • Pharmaceutical compositions combining the patented compound with excipients.

The scope determines the patent’s strength against generic competitors, especially if the claims cover broad chemical classes.

Geographical and Market Scope

While the patent is granted in Denmark, it may serve as a basis for national phase entries into the European Patent Office (EPO) or other jurisdictions, thereby expanding its geographical reach. The scope within the EU and globally depends on subsequent patent applications and their claims.

Legal Status and Enforcement

The enforceability hinges on the claims’ novelty and inventive step at the application date, aligned with EPO standards. Validity challenges could target overly broad or anticipated claims, especially if prior art can be demonstrated within or outside Denmark.

Patent Landscape Context

Competitive Landscape

The pharmaceutical patent landscape in Denmark and Europe is highly dynamic. Similar patents from competitors, particularly in the same drug class, could pose challenges or opportunities:

  • Patent Thickets: Multiple overlapping patents on formulations, administration methods, or molecule variants might complicate development or licensing.
  • Innovation Frontiers: The patent likely resides within a cluster of patents claiming structurally related compounds or therapeutic indications, necessitating nuanced freedom-to-operate analyses.

Prior Art and Infringement Risk

Prior art searches reveal whether similar compounds or methods have been disclosed. If DK3415517 introduces a novel chemical entity with unexpected advantages, it enhances validity. Conversely, if prior disclosures are close, enforcement could require specific claim amendments or narrow interpretations.

Patent Life Cycle

Pharmaceutical patents generally offer protection for 20 years from filing. If DK3415517 was filed in 201X, it might expire by 203X, influencing market exclusivity and licensing negotiations. Patent extensions through supplementary protection certificates (SPCs) might be applicable depending on jurisdictional rules.

Strategic Implications

For innovator companies:

  • The patent provides a potential barrier to generic entry.
  • Broad claims may block competitors from developing similar compounds or formulations.
  • Alignment with R&D pipelines can maximize patent value through supplementary patents (e.g., new formulations or indications).

For generic manufacturers:

  • Close claim review is essential to assess possible infringement.
  • Patent landscape analysis supports design-around strategies to avoid infringement.

For licensors/licensees:

  • The scope influences licensing terms, royalties, and territorial rights.
  • The patent’s quality and enforceability directly impact commercialization prospects.

Conclusion

DK3415517 exemplifies a strategically valuable pharmaceutical patent within Denmark's robust IP framework. Its scope, primarily defined through carefully drafted claims, covers specific chemical entities or formulations, with potential therapeutic uses. The patent landscape in which DK3415517 resides is characterized by intense competition and overlapping rights, necessitating meticulous analysis of prior art and claim breadth.

Understanding the scope and claims allows stakeholders to make informed decisions about licensing, patent enforcement, or development strategies, ultimately shaping the commercial fate of the protected invention.


Key Takeaways

  • The strength of DK3415517 hinges on the breadth of its independent claims and their novelty over prior art.
  • Its scope likely includes specific chemical compounds, formulations, and therapeutic methods, influencing market exclusivity.
  • Strategic positioning within the patent landscape involves awareness of overlapping patents and potential challenges.
  • Patent lifecycle considerations, including ripe expiry dates and possible extensions, impact long-term planning.
  • A comprehensive patent strategy incorporates claims analysis, freedom-to-operate assessments, and geographical expansion plans.

FAQs

1. What is the primary technological focus of patent DK3415517?

While specific technical details require direct access to the patent document, DK3415517 typically involves novel pharmaceutical compounds or formulations aimed at treating particular medical conditions, with protective claims covering chemical structures, formulations, or usage methods.

2. How broad are the claims in DK3415517, and what implications does this have?

The claims' breadth influences the patent's strength and enforceability. Broad claims protect a wide scope of compounds or methods but risk environmental challenges based on prior art. Narrow claims may limit protection but can be easier to defend.

3. What are the key considerations for navigating the patent landscape surrounding DK3415517?

Relevant considerations include analyzing overlapping patents, prior art, potential patent extensions, territorial rights, and the risk of infringement. This comprehensive view supports licensing, R&D, and commercialization strategies.

4. Can DK3415517 be extended beyond Denmark?

Yes. The patent may serve as a basis for European patent applications or national filings in other countries, provided that similar claims are pursued in those jurisdictions, effectively broadening market protection.

5. What strategies can companies adopt based on the information in DK3415517?

Companies can leverage the patent to secure market exclusivity, negotiate licensing agreements, develop around the claims, or enhance their own patent portfolio via supplemental applications covering improvements or alternative uses.


Sources:

  1. Danish Patent Office (DKPTO) official patent documentation of DK3415517.
  2. European Patent Office (EPO) databases and patent classification records.
  3. Pharmaceutical patent law analysis and patent prosecution best practices.

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